Journal: Bioinformatics

Volume 33, Issue 9

1271 -- 1277Birgit Debrabant. The null hypothesis of GSEA, and a novel statistical model for competitive gene set analysis
1278 -- 1285Zheng-Zheng Tang, Guanhua Chen, Alexander V. Alekseyenko, Hongzhe Li. A general framework for association analysis of microbial communities on a taxonomic tree
1286 -- 1292Dan Luo, Sara Ziebell, Lingling An. An informative approach on differential abundance analysis for time-course metagenomic sequencing data
1293 -- 1300Joël Lafond-Lapalme, Marc-Olivier Duceppe, Shengrui Wang, Peter Moffett, Benjamin Mimee. A new method for decontamination of de novo transcriptomes using a hierarchical clustering algorithm
1301 -- 1308Chen Sun, Paul Medvedev. VarMatch: robust matching of small variant datasets using flexible scoring schemes
1309 -- 1316Qiang Kou, Si Wu, Nikola Tolic, Ljiljana Pasa-Tolic, Yunlong Liu, Xiaowen Liu. A mass graph-based approach for the identification of modified proteoforms using top-down tandem mass spectra
1317 -- 1323Masae Hosoda, Yukie Akune, Kiyoko F. Aoki-Kinoshita. Development and application of an algorithm to compute weighted multiple glycan alignments
1324 -- 1330Hamid Mohamadi, Hamza Khan, Inanç Birol. ntCard: a streaming algorithm for cardinality estimation in genomics data
1331 -- 1337Quan Le, Fabian Sievers, Desmond G. Higgins. Protein multiple sequence alignment benchmarking through secondary structure prediction
1338 -- 1345Jeremy Adams, Michael J. Mansfield, Daniel J. Richard, Andrew C. Doxey. Lineage-specific mutational clustering in protein structures predicts evolutionary shifts in function
1346 -- 1353Claire Marks, Jaroslaw Nowak, Stefan Klostermann, Guy Georges, James Dunbar, Jiye Shi, Sebastian Kelm, Charlotte M. Deane. Sphinx: merging knowledge-based and ab initio approaches to improve protein loop prediction
1354 -- 1361Sean Maxwell, Mark R. Chance, Mehmet Koyutürk. Linearity of network proximity measures: implications for set-based queries and significance testing
1362 -- 1369Olga Nikolova, Russell Moser, Christopher Kemp, Mehmet Gönen, Adam A. Margolin. Modeling gene-wise dependencies improves the identification of drug response biomarkers in cancer studies
1370 -- 1378Yifan Yang, Lei Xu, Zheyun Feng, Jeffrey A. Cruz, Linda J. Savage, David M. Kramer 0001, Jin Chen. PhenoCurve: capturing dynamic phenotype-environment relationships using phenomics data
1379 -- 1386Philipp Hanslovsky, John A. Bogovic, Stephan Saalfeld. Image-based correction of continuous and discontinuous non-planar axial distortion in serial section microscopy
1387 -- 1388Yan Holtz, Jacques David, Vincent Ranwez. The genetic map comparator: a user-friendly application to display and compare genetic maps
1389 -- 1391Audrey Lemaçon, Charles Joly Beauparlant, Penny Soucy, Jamie Allen, Douglas F. Easton, Peter Kraft, Jacques Simard, Arnaud Droit. VEXOR: an integrative environment for prioritization of functional variants in fine-mapping analysis
1392 -- 1393E. Drori, D. Levy, P. Smirin-Yosef, O. Rahimi, M. Salmon-Divon. CircosVCF: circos visualization of whole-genome sequence variations stored in VCF files
1394 -- 1395Martin Sosic, Mile Sikic. Edlib: a C/C ++ library for fast, exact sequence alignment using edit distance
1396 -- 1398Yongchao Liu, Fabian Ripp, Rene Koeppel, Hanno Schmidt, Sören Lukas Hellmann, Mathias Weber, Christopher Felix Krombholz, Bertil Schmidt, Thomas Hankeln. AFS: identification and quantification of species composition by metagenomic sequencing
1399 -- 1401Yong Qian, Thomas J. Butler, Krista Opsahl-Ong, Nicholas S. Giroux, Carlo Sidore, Ramaiah Nagaraja, Francesco Cucca, Luigi Ferrucci, Gonçalo R. Abecasis, David Schlessinger, Jun Ding. fastMitoCalc: an ultra-fast program to estimate mitochondrial DNA copy number from whole-genome sequences
1402 -- 1404Marco Necci, Damiano Piovesan, Zsuzsanna Dosztányi, Silvio C. E. Tosatto. MobiDB-lite: fast and highly specific consensus prediction of intrinsic disorder in proteins
1405 -- 1406Siqi Tian, Rhiju Das. Primerize-2D: automated primer design for RNA multidimensional chemical mapping
1407 -- 1410Raziur Rahman, John Otridge, Ranadip Pal. IntegratedMRF: random forest-based framework for integrating prediction from different data types
1411 -- 1413Izaskun Mallona, Anna Díez-Villanueva, Berta Martín, Miguel A. Peinado. Chainy: an universal tool for standardized relative quantification in real-time PCR
1414 -- 1415Richard H. Adams, Drew R. Schield, Daren C. Card, Heath Blackmon, Todd A. Castoe. GppFst: genomic posterior predictive simulations of FST and dXY for identifying outlier loci from population genomic data
1416 -- 1417Ivan Krukov, Bianca De Sanctis, A. P. Jason de Koning. Wright-Fisher exact solver (WFES): scalable analysis of population genetic models without simulation or diffusion theory
1418 -- 1420Fotis E. Psomopoulos, Dimitrios M. Vitsios, Shakuntala Baichoo, Christos A. Ouzounis. BioPAXViz: a cytoscape application for the visual exploration of metabolic pathway evolution
1421 -- 1423Laurent Heirendt, Ines Thiele, Ronan M. T. Fleming. DistributedFBA.jl: high-level, high-performance flux balance analysis in Julia
1424 -- 1425Surya Gupta, Veronic De Puysseleyr, José Van der Heyden, Davy Maddelein, Irma Lemmens, Sam Lievens, Sven Degroeve, Jan Tavernier, Lennart Martens. MAPPI-DAT: data management and analysis for protein-protein interaction data from the high-throughput MAPPIT cell microarray platform
1426 -- 1428John Christian Givhan Spainhour, JuHo Lim, Peng Qiu. GDISC: a web portal for integrative analysis of gene-drug interaction for survival in cancer
1429 -- 0Izaskun Mallona, Anna Díez-Villanueva, Berta Martín, Miguel A. Peinado. Chainy: an universal tool for standardized relative quantification in real-time PCR

Volume 33, Issue 8

1111 -- 1115Scott D. Brown, Greg Hapgood, Christian Steidl, Andrew P. Weng, Kerry J. Savage. Defining the clonality of peripheral T cell lymphomas using RNA-seq
1116 -- 1120Kasper Harpsøe, Michael W. Boesgaard, Christian Munk, Hans Bräuner-Osborne, David E. Gloriam. Structural insight to mutation effects uncover a common allosteric site in class C GPCRs
1121 -- 1129Li Zhu, Ying Ding, Cho-Yi Chen, Lin Wang, Zhiguang Huo. MetaDCN: meta-analysis framework for differential co-expression network detection with an application in breast cancer
1130 -- 1138Weicai Ye, Ying Chen, Yongdong Zhang, Yuesheng Xu. H-BLAST: a fast protein sequence alignment toolkit on heterogeneous computers with GPUs
1139 -- 1146Yongjun Piao, Seongkeon Lee, Eun-Joon Lee, Keith D. Robertson, Huidong Shi. CAME: identification of chromatin accessibility from nucleosome occupancy and methylome sequencing
1147 -- 1153Suyash S. Shringarpure, Rasika A. Mathias, Ryan D. Hernandez, Timothy D. O'Connor, Zachary A. Szpiech. Using genotype array data to compare multi- and single-sample variant calls and improve variant call sets from deep coverage whole-genome sequencing data
1154 -- 1159Mateusz Kaduk, Erik L. L. Sonnhammer. Improved orthology inference with Hieranoid 2
1160 -- 1168Ignazio Carbone, James B. White, Jolanta Miadlikowska, A. Elizabeth Arnold, Mark A. Miller. T-BAS: Tree-Based Alignment Selector toolkit for phylogenetic-based placement, alignment downloads and metadata visualization: an example with the Pezizomycotina tree of life
1169 -- 1178Jean-Pierre Séhi Glouzon, Jean-Pierre Perreault, Shengrui Wang. The super-n-motifs model: a novel alignment-free approach for representing and comparing RNA secondary structures
1179 -- 1186Davis J. McCarthy, Kieran R. Campbell, Aaron T. L. Lun, Quin F. Wills. Scater: pre-processing, quality control, normalization and visualization of single-cell RNA-seq data in R
1187 -- 1196Xujun Liang, Pengfei Zhang, Lu Yan, Ying Fu, Fang Peng. LRSSL: predict and interpret drug-disease associations based on data integration using sparse subspace learning
1197 -- 1204Gui-Min Qin, Rui-Yi Li, Xing-Ming Zhao. PhosD: inferring kinase-substrate interactions based on protein domains
1205 -- 1209Andreas Helfenstein, Päivi Tammela. Analyzing user-generated online content for drug discovery: development and use of MedCrawler
1210 -- 1215Xiaoling Chen, Jeffrey T. Chang. Planning bioinformatics workflows using an expert system
1216 -- 1217Hajk-Georg Drost, Jerzy Paszkowski. Biomartr: genomic data retrieval with R
1218 -- 1220Seung-Hyuk Choi, Hyunwoo Kim, Eunok Paek. ACTG: novel peptide mapping onto gene models
1221 -- 1223Pablo Mier, Miguel A. Andrade-Navarro. dAPE: a web server to detect homorepeats and follow their evolution
1224 -- 1226Andrzej Zielezinski, Michal Dziubek, Jan Sliski, Wojciech M. Karlowski. ORCAN - a web-based meta-server for real-time detection and functional annotation of orthologs
1227 -- 1229Ian Holmes. Historian: accurate reconstruction of ancestral sequences and evolutionary rates
1230 -- 1232Lionel Guy. phyloSkeleton: taxon selection, data retrieval and marker identification for phylogenomics
1233 -- 1234Matthew Colledge, B. A. Wallace. AnglerFish: a webserver for defining the geometry of α-helices in membrane proteins
1235 -- 1237Ling Wang, Xiaoqian Pang, Yecheng Li, Ziying Zhang, WenAn Tan. RADER: a RApid DEcoy Retriever to facilitate decoy based assessment of virtual screening
1238 -- 1240Thomas Litfin, Yaoqi Zhou, Yuedong Yang. SPOT-ligand 2: improving structure-based virtual screening by binding-homology search on an expanded structural template library
1241 -- 1242Kieran R. Campbell, Christopher Yau. switchde: inference of switch-like differential expression along single-cell trajectories
1243 -- 1245Peter J. van der Most, Leanne K. Küpers, Harold Snieder, Ilja M. Nolte. QCEWAS: automated quality control of results of epigenome-wide association studies
1246 -- 1247Alexandre Fournier-Level, Charles Robin, David J. Balding. GWAlpha: genome-wide estimation of additive effects (alpha) based on trait quantile distribution from pool-sequencing experiments
1248 -- 1249Gennaro Gambardella, Matteo Cereda, Lorena Benedetti, Francesca D. Ciccarelli. MEGA-V: detection of variant gene sets in patient cohorts
1250 -- 1252Alberto Franzin, Francesco Sambo, Barbara Di Camillo. bnstruct: an R package for Bayesian Network structure learning in the presence of missing data
1253 -- 1254Frank T. Bergmann, David P. Nickerson, Dagmar Waltemath, Martin Scharm. SED-ML web tools: generate, modify and export standard-compliant simulation studies
1255 -- 1257Sébastien Carrère, Jérôme Gouzy. myGenomeBrowser: building and sharing your own genome browser
1258 -- 1260Jiewen Du, Xin Yan, Zhihong Liu, Lu Cui, Peng Ding. cBinderDB: a covalent binding agent database
1261 -- 1270Justin Chu, Hamid Mohamadi, René L. Warren, Chen Yang, Inanç Birol. Innovations and challenges in detecting long read overlaps: an evaluation of the state-of-the-art

Volume 33, Issue 7

951 -- 955Mattia Cinelli, Yuxin Sun, Katharine Best, James M. Heather, Shlomit Reich-Zeliger. Feature selection using a one dimensional naïve Bayes' classifier increases the accuracy of support vector machine classification of CDR3 repertoires
956 -- 963Bryan Quach, Terrence S. Furey. DeFCoM: analysis and modeling of transcription factor binding sites using a motif-centric genomic footprinter
964 -- 970Arash Bayat, Bruno Gaëta, Aleksandar Ignjatovic, Sri Parameswaran. Improved VCF normalization for accurate VCF comparison
971 -- 979Chris-Andre Leimeister, Salma Sohrabi-Jahromi, Burkhard Morgenstern. Fast and accurate phylogeny reconstruction using filtered spaced-word matches
980 -- 987Edwin Jacox, Mathias Weller, Eric Tannier, Céline Scornavacca. Resolution and reconciliation of non-binary gene trees with transfers, duplications and losses
988 -- 996Sinan Ugur Umu, Paul P. Gardner. A comprehensive benchmark of RNA-RNA interaction prediction tools for all domains of life
997 -- 1004Frédéric Cazals, Tom Dreyfus. The structural bioinformatics library: modeling in biomolecular science and beyond
1005 -- 1013James H. Collier, Lloyd Allison, Arthur M. Lesk, Peter J. Stuckey, Maria Garcia de la Banda. Statistical inference of protein structural alignments using information and compression
1014 -- 1020Surendra S. Negi, Werner Braun. Cross-React: a new structural bioinformatics method for predicting allergen cross-reactivity
1021 -- 1030Sajad Mirzaei, Yufeng Wu. RENT+: an improved method for inferring local genealogical trees from haplotypes with recombination
1031 -- 1039Yang Chen, Rong Xu. Context-sensitive network-based disease genetics prediction and its implications in drug discovery
1040 -- 1048Itziar Irurzun-Arana, José Martín Pastor, Iñaki F. Trocóniz, José David Gómez-Mantilla. Advanced Boolean modeling of biological networks applied to systems pharmacology
1049 -- 1056Fabian Fröhlich, Fabian J. Theis, Joachim O. Rädler, Jan Hasenauer. Parameter estimation for dynamical systems with discrete events and logical operations
1057 -- 1063Ehsan Motamedian, Maryam Mohammadi, Seyed Abbas Shojaosadati, Mona Heydari. TRFBA: an algorithm to integrate genome-scale metabolic and transcriptional regulatory networks with incorporation of expression data
1064 -- 1072George Teodoro, Tahsin M. Kurç, Luis F. R. Taveira, Alba C. M. A. Melo, Yi Gao. Algorithm sensitivity analysis and parameter tuning for tissue image segmentation pipelines
1073 -- 1080Miroslav Radojevic, Erik Meijering. Automated neuron tracing using probability hypothesis density filtering
1081 -- 1082Thomas Lin Pedersen, Intawat Nookaew, David Wayne Ussery, Maria Månsson. PanViz: interactive visualization of the structure of functionally annotated pangenomes
1083 -- 1085Liron Ganel, Haley J. Abel, FinMetSeq Consortium, Ira M. Hall. SVScore: an impact prediction tool for structural variation
1086 -- 1089Maciej Dlugosz, Sebastian Deorowicz. RECKONER: read error corrector based on KMC
1090 -- 1092Wei Zhou, Ruilin Li, Shuo Yuan, Changchun Liu, Shaowen Yao. MetaSpark: a spark-based distributed processing tool to recruit metagenomic reads to reference genomes
1093 -- 1095Luyang Huo, Han Zhang, Xueting Huo, Yasong Yang, Xueqiong Li. pHMM-tree: phylogeny of profile hidden Markov models
1096 -- 1098Irina Balaur, Alexander Mazein, Mansoor Saqi, Artem Lysenko, Christopher J. Rawlings. Recon2Neo4j: applying graph database technologies for managing comprehensive genome-scale networks
1099 -- 1100Sudeepta Kumar Panda, Sanjay V. Boddul, Guillermina Yanek Jiménez-Andrade, Long Jiang, Zsolt Kasza. Green listed - a CRISPR screen tool
1101 -- 1103Ravi D. Shankar, Sanchita Bhattacharya, Chethan Jujjavarapu, Sandra Andorf, Jeffery A. Wiser. RImmPort: an R/Bioconductor package that enables ready-for-analysis immunology research data
1104 -- 1106Daniel Greene, Sylvia Richardson, Ernest Turro. ontologyX: a suite of R packages for working with ontological data
1107 -- 1109Ömer Nebil Yaveroglu, Noël Malod-Dognin, Tijana Milenkovic, Natasa Przulj. Rebuttal to the Letter to the Editor in response to the paper: proper evaluation of alignment-free network comparison methods

Volume 33, Issue 6

791 -- 798Yang Young Lu, Ting Chen, Jed A. Fuhrman, Fengzhu Sun. COCACOLA: binning metagenomic contigs using sequence COmposition, read CoverAge, CO-alignment and paired-end read LinkAge
799 -- 806Leena Salmela, Riku Walve, Eric Rivals, Esko Ukkonen. Accurate self-correction of errors in long reads using de Bruijn graphs
807 -- 813Joaquín Ezpeleta, Flavia J. Krsticevic, Pilar Bulacio, Elizabeth Tapia. Designing robust watermark barcodes for multiplex long-read sequencing
814 -- 821Yoo Ah Kim, Sanna Madan, Teresa M. Przytycka. WeSME: uncovering mutual exclusivity of cancer drivers and beyond
822 -- 833Hui-Yi Lin, Dung-Tsa Chen, Po-Yu Huang, Yung-Hsin Liu, Augusto Ochoa, Jovanny Zabaleta, Donald Mercante, Zhide Fang, Thomas A. Sellers, Julio M. Pow-Sang, Chia-Ho Cheng, Rosalind Eeles, Doug Easton, Zsofia Kote-Jarai, Ali Amin Al Olama, Sara Benlloch, Kenneth Muir, Graham G. Giles, Fredrik Wiklund, Henrik Gronberg, Christopher A. Haiman, Johanna Schleutker, Børge G. Nordestgaard, Ruth C. Travis, Freddie Hamdy, Nora Pashayan, Kay-Tee Khaw, Janet L. Stanford, William J. Blot, Stephen N. Thibodeau, Christiane Maier, Adam S. Kibel, Cezary Cybulski, Lisa A. Cannon-Albright, Hermann Brenner, Radka Kaneva, Jyotsna Batra, Manuel R. Teixeira, Hardev Pandha, Yong-Jie Lu, The PRACTICAL Consortium, Jong Y. Park. SNP interaction pattern identifier (SIPI): an intensive search for SNP-SNP interaction patterns
834 -- 842Linhao Jiang, Yichao Dong, Ning Chen, Ting Chen. DACE: a scalable DP-means algorithm for clustering extremely large sequence data
843 -- 853Hang Zhou, Yang Yang, Hong-bin Shen. Hum-mPLoc 3.0: prediction enhancement of human protein subcellular localization through modeling the hidden correlations of gene ontology and functional domain features
854 -- 862Xiaoli Zhang, Shiyong Liu. RBPPred: predicting RNA-binding proteins from sequence using SVM
863 -- 870Jiaqi Xia, Zhenling Peng, Dawei Qi, Hongbo Mu, Jianyi Yang. An ensemble approach to protein fold classification by integration of template-based assignment and support vector machine classifier
871 -- 878Feng Chen, Shuang Wang, Xiaoqian Jiang, Sijie Ding, Yao Lu, Jihoon Kim, Süleyman Cenk Sahinalp, Chisato Shimizu, Jane C. Burns, Victoria J. Wright, Eileen Png, Martin L. Hibberd, David D. Lloyd, Hai Yang, Amalio Telenti, Cinnamon S. Bloss, Dov Fox, Kristin E. Lauter, Lucila Ohno-Machado. PRINCESS: Privacy-protecting Rare disease International Network Collaboration via Encryption through Software guard extensionS
879 -- 885Anand Bhaskar, Adel Javanmard, Thomas A. Courtade, David Tse. Novel probabilistic models of spatial genetic ancestry with applications to stratification correction in genome-wide association studies
886 -- 892Hon-Cheong So, Pak C. Sham. Exploring the predictive power of polygenic scores derived from genome-wide association studies: a study of 10 complex traits
893 -- 900Matthew R. Long, Jennifer L. Reed. Improving flux predictions by integrating data from multiple strains
901 -- 908Zhen Gao, Yang Chen, XiaoShu Cai, Rong Xu. Predict drug permeability to blood-brain-barrier from clinical phenotypes: drug side effects and drug indications
909 -- 916Jessica S. Yu, Dante A. Pertusi, Adebola V. Adeniran, Keith E. J. Tyo. CellSort: a support vector machine tool for optimizing fluorescence-activated cell sorting and reducing experimental effort
917 -- 0Martin S. Lindner, Benjamin Strauch, Jakob M. Schulze, Simon H. Tausch, Piotr Wojtek Dabrowski, Andreas Nitsche, Bernhard Y. Renard. HiLive: real-time mapping of illumina reads while sequencing
920 -- 922Tilo Buschmann. DNABarcodes: an R package for the systematic construction of DNA sample tags
923 -- 925Alexey V. Kochetov, Jens Allmer, Alexandra I. Klimenko, Bulat S. Zuraev, Yury G. Matushkin, Sergey A. Lashin. AltORFev facilitates the prediction of alternative open reading frames in eukaryotic mRNAs
926 -- 928Michiaki Hamada, Yukiteru Ono, Kiyoshi Asai, Martin C. Frith. Training alignment parameters for arbitrary sequencers with LAST-TRAIN
929 -- 931Gauri Shende, Harshala Haldankar, Ram Shankar Barai, Mohammed Husain Bharmal, Vinit Shetty, Susan Idicula-Thomas. PBIT: Pipeline Builder for Identification of drug Targets for infectious diseases
932 -- 934Bradley R. Jones, Art F. Y. Poon. node.dating: dating ancestors in phylogenetic trees in R
935 -- 937Justas Dapkunas, Albertas Timinskas, Kliment Olechnovic, Mindaugas Margelevicius, Rytis Diciunas, Ceslovas Venclovas. The PPI3D web server for searching, analyzing and modeling protein-protein interactions in the context of 3D structures
938 -- 940Riccardo Panero, Antonio Rinaldi, Domenico Memoli, Giovanni Nassa, Maria Ravo, Francesca Rizzo, Roberta Tarallo, Luciano Milanesi, Alessandro Weisz, Giorgio Giurato. iSmaRT: a toolkit for a comprehensive analysis of small RNA-Seq data
941 -- 943Zefang Tang, Chenwei Li, Karena Zhang, Mingyu Yang, Xueda Hu. GE-mini: a mobile APP for large-scale gene expression visualization
944 -- 946Chuang Li, Tao Chen, Qiang He, Yunping Zhu, Kenli Li. MRUniNovo: an efficient tool for de novo peptide sequencing utilizing the hadoop distributed computing framework
947 -- 950Santiago Videla, Julio Saez-Rodriguez, Carito Guziolowski, Anne Siegel. caspo: a toolbox for automated reasoning on the response of logical signaling networks families

Volume 33, Issue 5

631 -- 639Pranjal Vachaspati, Tandy J. Warnow. FastRFS: fast and accurate Robinson-Foulds Supertrees using constrained exact optimization
640 -- 649Charlotte A. Darby, Maureen Stolzer, Patrick J. Ropp, Daniel Barker, Dannie Durand. Xenolog classification
650 -- 653Denye Ogeh, Richard Badge. A pipeline for local assembly of minisatellite alleles from single-molecule sequencing data
654 -- 660Agnès Lagnoux, Sabine Mercier, Pierre Vallois. Statistical significance based on length and position of the local score in a model of i.i.d. sequences
661 -- 668Jyun-Rong Wang, Wen-Lin Huang, Ming-Ju Tsai, Kai-Ti Hsu, Hui-Ling Huang, Shinn-Ying Ho. ESA-UbiSite: accurate prediction of human ubiquitination sites by identifying a set of effective negatives
669 -- 676Xavier Meyer, Bastien Chopard, Nicolas Salamin. Accelerating Bayesian inference for evolutionary biology models
677 -- 684Tong Wang, Yuedong Yang, Yaoqi Zhou, Haipeng Gong. LRFragLib: an effective algorithm to identify fragments for de novo protein structure prediction
685 -- 692Jack Hanson, Yuedong Yang, Kuldip K. Paliwal, Yaoqi Zhou. Improving protein disorder prediction by deep bidirectional long short-term memory recurrent neural networks
693 -- 700Cristóbal Fresno, Germán González, Gabriela Alejandra Merino, Ana Georgina Flesia, Osvaldo L. Podhajcer, Andrea S. Llera, Elmer Andrés Fernández. A novel non-parametric method for uncertainty evaluation of correlation-based molecular signatures: its application on PAM50 algorithm
701 -- 709Frederik Gwinner, Gwénola Boulday, Claire Vandiedonck, Minh Arnould, Cécile Cardoso, Iryna Nikolayeva, Oriol Guitart Pla, Cécile V. Denis, Olivier D. Christophe, Johann Beghain, Elisabeth Tournier-Lasserve, Benno Schwikowski. Network-based analysis of omics data: the LEAN method
710 -- 717Steven S. Andrews. Smoldyn: particle-based simulation with rule-based modeling, improved molecular interaction and a library interface
718 -- 725Corinna Maier, Carolin Loos, Jan Hasenauer. Robust parameter estimation for dynamical systems from outlier-corrupted data
726 -- 732Arya A. Das, T. Ajayakumar Darsana, Elizabeth Jacob. Agent-based re-engineering of ErbB signaling: a modeling pipeline for integrative systems biology
733 -- 739Xing Chen, Yu-An Huang, Zhu-Hong You, Guiying Yan, Xuesong Wang. A novel approach based on KATZ measure to predict associations of human microbiota with non-infectious diseases
740 -- 742Elizabeth Baskin, Rick Farouni, Ewy A. Mathé. ALTRE: workflow for defining ALTered Regulatory Elements using chromatin accessibility data
743 -- 745Hongliang Mao, Hao Wang. SINE_scan: an efficient tool to discover short interspersed nuclear elements (SINEs) in large-scale genomic datasets
746 -- 748Pedro Madrigal. fCCAC: functional canonical correlation analysis to evaluate covariance between nucleic acid sequencing datasets
749 -- 750Shibiao Wan, Man-Wai Mak, Sun-Yuan Kung. FUEL-mLoc: feature-unified prediction and explanation of multi-localization of cellular proteins in multiple organisms
751 -- 753Jeremiah Wala, Rameen Beroukhim. SeqLib: a C ++ API for rapid BAM manipulation, sequence alignment and sequence assembly
754 -- 756Julia Koehler Leman, Benjamin K. Mueller, Jeffrey J. Gray. Expanding the toolkit for membrane protein modeling in Rosetta
757 -- 759Jil Sander, Joachim L. Schultze, Nir Yosef. ImpulseDE: detection of differentially expressed genes in time series data using impulse models
760 -- 761Tomas Puelma, Viviana Araus, Javier Canales, Elena A. Vidal, Juan M. Cabello, Alvaro Soto, Rodrigo A. Gutiérrez. GENIUS: web server to predict local gene networks and key genes for biological functions
762 -- 763Ethan Bahl, Tanner Koomar, Jacob J. Michaelson. cerebroViz: an R package for anatomical visualization of spatiotemporal brain data
764 -- 766Alicia T. Specht, Jun Li. LEAP: constructing gene co-expression networks for single-cell RNA-sequencing data using pseudotime ordering
767 -- 769Andrian Yang, Michael Troup, Peijie Lin, Joshua W. K. Ho. Falco: a quick and flexible single-cell RNA-seq processing framework on the cloud
770 -- 772Hannes Klarner, Adam Streck, Heike Siebert. PyBoolNet: a python package for the generation, analysis and visualization of boolean networks
773 -- 775Andrea Rodriguez-Martinez, Rafael Ayala, Joram M. Posma, Ana L. Neves, Dominique Gauguier, Jeremy K. Nicholson, Marc-Emmanuel Dumas. MetaboSignal: a network-based approach for topological analysis of metabotype regulation via metabolic and signaling pathways
776 -- 778B. Muchmore, M. E. Alarcón-Riquelme. CymeR: cytometry analysis using KNIME, docker and R
779 -- 781Guillaume Gautreau, David Pejoski, Roger Le Grand, Antonio Cosma, Anne-Sophie Beignon, Nicolas Tchitchek. SPADEVizR: an R package for visualization, analysis and integration of SPADE results
782 -- 783Martha Zakrzewski, Carla Proietti, Jonathan J. Ellis, Shihab Hasan, Marie-Jo Brion, Bernard Berger, Lutz Krause. Calypso: a user-friendly web-server for mining and visualizing microbiome-environment interactions
784 -- 786Daniel A. Russell, Graham F. Hatfull. PhagesDB: the actinobacteriophage database
787 -- 788Sijin He, May Yong, Paul M. Matthews, Yike Guo. tranSMART-XNAT Connector tranSMART-XNAT connector - image selection based on clinical phenotypes and genetic profiles
789 -- 790Côme Pasqualin, François Gannier, Angèle Yu, Claire O. Malécot, Pierre Bredeloux, Véronique Maupoil. SarConfoCal: simultaneous sarcomere length and cytoplasmic calcium measurements for laser scanning confocal microscopy images

Volume 33, Issue 4

471 -- 474João Fadista, Nikolay Oskolkov, Ola Hansson, Leif Groop. LoFtool: a gene intolerance score based on loss-of-function variants in 60 706 individuals
475 -- 482Roye Rozov, Aya Brown Kav, David Bogumil, Naama Shterzer, Eran Halperin, Itzhak Mizrahi, Ron Shamir. Recycler: an algorithm for detecting plasmids from de novo assembly graphs
483 -- 490Hai Yang, Qiang Wei, Xue Zhong, Hushan Yang, Bingshan Li. Cancer driver gene discovery through an integrative genomics approach in a non-parametric Bayesian framework
491 -- 499Toby Dylan Hocking, Patricia Goerner-Potvin, Andreanne Morin, Xiaojian Shao, Tomi Pastinen, Guillaume Bourque. Optimizing ChIP-seq peak detectors using visual labels and supervised machine learning
500 -- 507Wei Jiang, Weichuan Yu. Controlling the joint local false discovery rate is more powerful than meta-analysis methods in joint analysis of summary statistics from multiple genome-wide association studies
508 -- 513Heydar Maboudi Afkham, Xuanbin Qiu, Matthew The, Lukas Käll. Uncertainty estimation of predictions of peptides' chromatographic retention times in shotgun proteomics
514 -- 521Janne H. Korhonen, Kimmo Palin, Jussi Taipale, Esko Ukkonen. Fast motif matching revisited: high-order PWMs, SNPs and indels
522 -- 528Weizhuang Zhou, Lichy Han, Russ B. Altman. Imputing gene expression to maximize platform compatibility
529 -- 536Raphael Petegrosso, SunHo Park, TaeHyun Hwang, Rui Kuang. Transfer learning across ontologies for phenome-genome association prediction
537 -- 544Ferhat Alkan, Cesim Erten. RedNemo: topology-based PPI network reconstruction via repeated diffusion with neighborhood modifications
545 -- 546Fabian Grandke, Rod Snowdon, Birgit Samans. gsrc: an R package for genome structure rearrangement calling
547 -- 548Emanuel Diego S. Penha, Egiebade Iriabho, Alex Dussaq, Diana Magalhaes de Oliveira, Jonas S. Almeida. Isomorphic semantic mapping of variant call format (VCF2RDF)
549 -- 551Diogo Almeida, Ida Skov, Artur Silva, Fabio Vandin, Qihua Tan, Richard Röttger, Jan Baumbach. Efficient detection of differentially methylated regions using DiMmeR
552 -- 554Blake L. Joyce, Asher Haug-Baltzell, Sean Davey, Matthew Bomhoff, James C. Schnable, Eric Lyons. FractBias: a graphical tool for assessing fractionation bias following polyploidy
555 -- 557Jin Zhang, Elaine R. Mardis, Christopher A. Maher. INTEGRATE-neo: a pipeline for personalized gene fusion neoantigen discovery
558 -- 560Jean-Philippe Fortin, Timothy Triche, Kasper D. Hansen. Preprocessing, normalization and integration of the Illumina HumanMethylationEPIC array with minfi
561 -- 563David C. Qian, Jonathan A. Busam, Xiangjun Xiao, Tracy A. O'Mara, Rosalind A. Eeles, Frederick R. Schumacher, Catherine M. Phelan, Christopher I. Amos. seXY: a tool for sex inference from genotype arrays
564 -- 565Diego J. Zea, Diego Anfossi, Morten Nielsen, Cristina Marino Buslje. MIToS.jl: mutual information tools for protein sequence analysis in the Julia language
566 -- 567Ankeeta Shah, Yingzhi Qian, Sebastien M. Weyn-Vanhentenryck, Chaolin Zhang. CLIP Tool Kit (CTK): a flexible and robust pipeline to analyze CLIP sequencing data
568 -- 570Jaroslaw Surkont, Yoan Diekmann, José B. Pereira-Leal. Rabifier2: an improved bioinformatic classifier of Rab GTPases
571 -- 573Ahmed Arslan, Vera van Noort. yMap: an automated method to map yeast variants to protein modifications and functional regions
574 -- 576Daniel Mapleson, Gonzalo Garcia Accinelli, George Kettleborough, Jonathan Wright, Bernardo J. Clavijo. KAT: a K-mer analysis toolkit to quality control NGS datasets and genome assemblies
577 -- 579Gabriel Renaud, Kristian Hanghøj, Eske Willerslev, Ludovic Orlando. gargammel: a sequence simulator for ancient DNA
580 -- 582Ralf Eggeling, Ivo Grosse, Jan Grau. InMoDe: tools for learning and visualizing intra-motif dependencies of DNA binding sites
583 -- 585Carlos García-Pérez, Rafael Peláez, Roberto Therón, José Luis López-Pérez. JADOPPT: java based AutoDock preparing and processing tool
586 -- 588Renzhi Cao, Badri Adhikari, Debswapna Bhattacharya, Miao Sun, Jie Hou, Jianlin Cheng. QAcon: single model quality assessment using protein structural and contact information with machine learning techniques
589 -- 591Renana Sabi, Renana Volvovitch Daniel, Tamir Tuller. stAIcalc: tRNA adaptation index calculator based on species-specific weights
592 -- 593Stefan J. Haunsberger, Niamh M. C. Connolly, Jochen H. M. Prehn. miRNAmeConverter: an R/bioconductor package for translating mature miRNA names to different miRBase versions
594 -- 595Joseph H. Marcus, John Novembre. Visualizing the geography of genetic variants
596 -- 598Jan Schröder, Vincent Corbin, Anthony T. Papenfuss. HYSYS: have you swapped your samples?
599 -- 600Arthur Wuster, Diana Chang, Timothy W. Behrens, Tushar Bhangale. geneAttribution: trait agnostic identification of candidate genes associated with noncoding variation
601 -- 604Julian Schwab, Andre Burkovski, Lea Siegle, Christoph Müssel, Hans A. Kestler. ViSiBooL - visualization and simulation of Boolean networks with temporal constraints
605 -- 607Alberto Noronha, Anna Dröfn Daníelsdóttir, Piotr Gawron, Freyr Jóhannsson, Soffía Jónsdóttir, Sindri Jarlsson, Jón Pétur Gunnarsson, Sigurður Brynjólfsson, Reinhard Schneider, Ines Thiele, Ronan M. T. Fleming. ReconMap: an interactive visualization of human metabolism
608 -- 611Tolutola Oyetunde, Muhan Zhang, Yixin Chen, Yinjie J. Tang, Cynthia Lo. BoostGAPFILL: improving the fidelity of metabolic network reconstructions through integrated constraint and pattern-based methods
612 -- 614Sara Ballouz, Melanie Weber 0001, Paul Pavlidis, Jesse Gillis. EGAD: ultra-fast functional analysis of gene networks
615 -- 617Bhusan K. Kuntal, Sharmila S. Mande. Web-igloo: a web based platform for multivariate data visualization
618 -- 620Dayne L. Filer, Parth Kothiya, R. Woodrow Setzer, Richard S. Judson, Matthew T. Martin. tcpl: the ToxCast pipeline for high-throughput screening data
621 -- 623Stefano Cacciatore, Leonardo Tenori, Claudio Luchinat, Phillip R. Bennett, David MacIntyre. KODAMA: an R package for knowledge discovery and data mining
624 -- 626Adrian Bickerstaffe, Thilina Ranaweera, Travis Endersby, Christopher Ellis, Sanjaya Maddumarachchi, George E. Gooden, Paul White, Eric K. Moses, Alex W. Hewitt, John L. Hopper. The Ark: a customizable web-based data management tool for health and medical research
627 -- 628Nicholas A. Watts, Frank Alex Feltus. Big Data Smart Socket (BDSS): a system that abstracts data transfer habits from end users
629 -- 630Mark C. Hiner, Curtis T. Rueden, Kevin W. Eliceiri. ImageJ-MATLAB: a bidirectional framework for scientific image analysis interoperability

Volume 33, Issue 3

311 -- 319Alden King-Yung Leung, Tsz-Piu Kwok, Raymond Wan, Ming Xiao, Pui-Yan Kwok, Kevin Y. Yip, Ting-Fung Chan. OMBlast: alignment tool for optical mapping using a seed-and-extend approach
320 -- 326Serge Moulin, Nicolas Seux, Stéphane Chrétien, Christophe Guyeux, Emmanuelle Lerat. Simulation-based estimation of branching models for LTR retrotransposons
327 -- 333Sufang Wang, Michael Gribskov. Comprehensive evaluation of de novo transcriptome assembly programs and their effects on differential gene expression analysis
334 -- 340Ilham A. Shahmuradov, Rozaimi Mohamad Razali, Salim Bougouffa, Aleksandar Radovanovic, Vladimir B. Bajic. bTSSfinder: a novel tool for the prediction of promoters in cyanobacteria and Escherichia coli
341 -- 346Xiang Cheng, Shu-Guang Zhao, Xuan Xiao, Kuo-Chen Chou. iATC-mISF: a multi-label classifier for predicting the classes of anatomical therapeutic chemicals
347 -- 353Castrense Savojardo, Pier Luigi Martelli, Piero Fariselli, Rita Casadio. SChloro: directing Viridiplantae proteins to six chloroplastic sub-compartments
354 -- 362Iakov I. Davydov, Marc Robinson-Rechavi, Nicolas Salamin. State aggregation for fast likelihood computations in molecular evolution
363 -- 372Shuaibing He, Manman Li, Xiaotong Ye, Hongyu Wang, Wenkang Yu, Wenjing He, Yun Wang, Yanjiang Qiao. Site of metabolism prediction for oxidation reactions mediated by oxidoreductases based on chemical bond
373 -- 381Saulo Henrique Pires de Oliveira, Jiye Shi, Charlotte M. Deane. Comparing co-evolution methods and their application to template-free protein structure prediction
382 -- 389Christopher L. Barrett, Fenix W. D. Huang, Christian M. Reidys. Sequence-structure relations of biopolymers
390 -- 396Dmytro Guzenko, Sergei V. Strelkov. Granular clustering of de novo protein models
397 -- 404Roman Hornung, David Causeur, Christoph Bernau, Anne-Laure Boulesteix. Improving cross-study prediction through addon batch effect adjustment or addon normalization
405 -- 413Lili Liu, Zijun Zhang, Taotao Sheng, Ming Chen. DEF: an automated dead-end filling approach based on quasi-endosymbiosis
414 -- 424Monther Alhamdoosh, Milica Ng, Nicholas J. Wilson, Julie M. Sheridan, Huy Huynh, Michael J. Wilson, Matthew E. Ritchie. Combining multiple tools outperforms individual methods in gene set enrichment analyses
425 -- 427Stefan Canzar, Karlynn E. Neu, Qingming Tang, Patrick C. Wilson, Aly A. Khan. BASIC: BCR assembly from single cells
428 -- 431Phuc-Loi Luu, Daniela Gerovska, Mikel Arrospide-Elgarresta, Sugoi Retegi-Carrión, Hans R. Schöler, Marcos J. Araúzo-Bravo. P3BSseq: parallel processing pipeline software for automatic analysis of bisulfite sequencing data
432 -- 434Ekaterina A. Khramtsova, Barbara E. Stranger. Assocplots: a Python package for static and interactive visualization of multiple-group GWAS results
435 -- 437Vojtech Bystrý, Tomas Reigl, Adam Krejci, Martin Demko, Barbora Hanakova, Andrea Grioni, Henrik Knecht, Max Schlitt, Peter Dreger, Leopold Sellner, Dietrich Herrmann, Marine Pingeon, Myriam Boudjoghra, Jos Rijntjes, Christiane Pott, Anton W. Langerak, Patricia J. T. A. Groenen, Frederic Davi, Monika Brüggemann, Nikos Darzentas, also on Behalf of EuroClonality-NGS. ARResT/Interrogate: an interactive immunoprofiler for IG/TR NGS data
438 -- 440Xingjian Xu, Zhaohua Ji, Zhang Zhang. CloudPhylo: a fast and scalable tool for phylogeny reconstruction
441 -- 443Krishna Choudhary, Luyao Ruan, Fei Deng, Nathan P. Shih, Sharon Aviran. SEQualyzer: interactive tool for quality control and exploratory analysis of high-throughput RNA structural profiling data
444 -- 446Giacomo Janson, Chengxin Zhang, Maria Giulia Prado, Alessandro Paiardini. PyMod 2.0: improvements in protein sequence-structure analysis and homology modeling within PyMOL
447 -- 449Jonathan W. Nelson, Jiri Sklenar, Anthony P. Barnes, Jessica Minnier. The START App: a web-based RNAseq analysis and visualization resource
450 -- 452Yu Zhang, Juan Xie, Jinyu Yang, Anne Fennell, Chi Zhang, Qin Ma. QUBIC: a bioconductor package for qualitative biclustering analysis of gene co-expression data
453 -- 455Luca Bianco, Samantha Riccadonna, Enrico Lavezzo, Marco Falda, Elide Formentin, Duccio Cavalieri, Stefano Toppo, Paolo Fontana. Pathway Inspector: a pathway based web application for RNAseq analysis of model and non-model organisms
456 -- 457Elisa Salviato, Vera Djordjilovic, Monica Chiogna, Chiara Romualdi. simPATHy: a new method for simulating data from perturbed biological PATHways
458 -- 460Wei Lan, Min Li, Kaijie Zhao, Jin Liu, Fang-Xiang Wu, Yi Pan, Jianxin Wang. LDAP: a web server for lncRNA-disease association prediction
461 -- 463Thomas Van Parys, Ine Melckenbeeck, Maarten Houbraken, Pieter Audenaert, Didier Colle, Mario Pickavet, Piet Demeester, Yves Van de Peer. A Cytoscape app for motif enumeration with ISMAGS
464 -- 466Daniel P. Russo, Marlene T. Kim, Wenyi Wang, Daniel Pinolini, Sunil M. Shende, Judy Strickland, Thomas Hartung, Hao Zhu. CIIPro: a new read-across portal to fill data gaps using public large-scale chemical and biological data
467 -- 469Zhi-Yong Liang, Hong-Yan Lai, Huan Yang, Chang-Jian Zhang, Hui Yang, Huan-Huan Wei, Xin-Xin Chen, Ya-Wei Zhao, Zhen-Dong Su, Wen-Chao Li, En-Ze Deng, Hua Tang, Wei Chen, Hao Lin. Pro54DB: a database for experimentally verified sigma-54 promoters
470 -- 0Dalia Cohn-Alperovich, Alona Rabner, Ilona Kifer, Yael Mandel-Gutfreund, Zohar Yakhini. Mutual enrichment in aggregated ranked lists with applications to gene expression regulation

Volume 33, Issue 24

3871 -- 3877Mehmet Tekman, Alan Medlar, Monika Mozere, Robert Kleta, Horia Stanescu. HaploForge: a comprehensive pedigree drawing and haplotype visualization web application
3878 -- 3886Jin Liu, Xiang Wan, Chaolong Wang, Chao Yang, Xiaowei Zhou, Can Yang. LLR: a latent low-rank approach to colocalizing genetic risk variants in multiple GWAS
3887 -- 3894Minli Bao, Kai Wang. Genome-wide association studies using a penalized moving-window regression
3895 -- 3901Nilah M. Ioannidis, Joe R. Davis, Marianne K. DeGorter, Nicholas B. Larson, Shannon K. McDonnell, Amy J. French, Alexis J. Battle, Trevor J. Hastie, Stephen N. Thibodeau, Stephen B. Montgomery, Carlos D. Bustamante, Weiva Sieh, Alice S. Whittemore. FIRE: functional inference of genetic variants that regulate gene expression
3902 -- 3908Gabriele Orlando, Daniele Raimondi, Taushif Khan, Tom Lenaerts, Wim F. Vranken. SVM-dependent pairwise HMM: an application to protein pairwise alignments
3909 -- 3916Duolin Wang, Shuai Zeng, Chunhui Xu, Wangren Qiu, Yanchun Liang, Trupti Joshi, Dong Xu. MusiteDeep: a deep-learning framework for general and kinase-specific phosphorylation site prediction
3917 -- 3921Martin Christen Frølund Thomsen, Henrik Hasman, Henrik Westh, Hülya Kaya, Ole Lund. RUCS: rapid identification of PCR primers for unique core sequences
3922 -- 3928Brandon Pickett, Justin Miller, Perry G. Ridge. Kmer-SSR: a fast and exhaustive SSR search algorithm
3929 -- 3937Wolfgang Kopp, Martin Vingron. An improved compound Poisson model for the number of motif hits in DNA sequences
3938 -- 3946Alexander Yermanos, Victor Greiff, Nike Julia Krautler, Ulrike Menzel, Andreas Dounas, Enkelejda Miho, Annette Oxenius, Tanja Stadler, Sai T. Reddy. Comparison of methods for phylogenetic B-cell lineage inference using time-resolved antibody repertoire simulations (AbSim)
3947 -- 3954Emma E. Kim, Seunghoon Lee, Cue Hyunkyu Lee, Hyunjung Oh, Kyuyoung Song, Buhm Han. FOLD: a method to optimize power in meta-analysis of genetic association studies with overlapping subjects
3955 -- 3963Aravind Sankar, Sayan Ranu, Karthik Raman. Predicting novel metabolic pathways through subgraph mining
3964 -- 3972Yue Deng, Hector Zenil, Jesper Tegnér, Narsis A. Kiani. HiDi: an efficient reverse engineering schema for large-scale dynamic regulatory network reconstruction using adaptive differentiation
3973 -- 3981Simon Baker, Imran Ali, Ilona Silins, Sampo Pyysalo, Yufan Guo, Johan Högberg, Ulla Stenius, Anna Korhonen. Cancer Hallmarks Analytics Tool (CHAT): a text mining approach to organize and evaluate scientific literature on cancer
3982 -- 3984Yuan Tian, Tiffany J. Morris, Amy P. Webster, Zhen Yang, Stephan Beck, Andrew Feber, Andrew E. Teschendorff. ChAMP: updated methylation analysis pipeline for Illumina BeadChips
3985 -- 3987Virag Sharma, Peter Schwede, Michael Hiller. CESAR 2.0 substantially improves speed and accuracy of comparative gene annotation
3988 -- 3990Son Hoang Nguyen, Tania P. S. Duarte, Lachlan J. M. Coin, Minh Duc Cao. Real-time demultiplexing Nanopore barcoded sequencing data with npBarcode
3991 -- 3992Gilbert Deléage. ALIGNSEC: viewing protein secondary structure predictions within large multiple sequence alignments
3993 -- 3995Pieter Libin, Ewout Vanden Eynden, Francesca Incardona, Ann Nowé, Antonia Bezenchek, EucoHIV Study Group, Anders Sönnerborg, Anne-Mieke Vandamme, Kristof Theys, Guy Baele. PhyloGeoTool: interactively exploring large phylogenies in an epidemiological context
3996 -- 3998Enrico Guarnera, Zhen Wah Tan, Zejun Zheng, Igor N. Berezovsky. AlloSigMA: allosteric signaling and mutation analysis server
3999 -- 4000Massimiliano Bonomi, Carlo Camilloni. Integrative structural and dynamical biology with PLUMED-ISDB
4001 -- 4003Aurora Torrente, Alvis Brazma. clustComp, a bioconductor package for the comparison of clustering results
4004 -- 4006Alba Gutiérrez-Sacristán, Carles Hernandez-Ferrer, Juan R. González, Laura Inés Furlong. psygenet2r: a R/Bioconductor package for the analysis of psychiatric disease genes
4007 -- 4009Yoann Gloaguen, Fraser Morton, Rónán Daly, Ross Gurden, Simon Rogers, Joe Wandy, David Wilson, Michael Barrett, Karl Burgess. PiMP my metabolome: an integrated, web-based tool for LC-MS metabolomics data
4010 -- 4011Enyu Dai, Feng Yang, Jing Wang, Xu Zhou, Qian Song, Weiwei An, Lihong Wang, Wei Jiang. ncDR: a comprehensive resource of non-coding RNAs involved in drug resistance
4012 -- 4014Stefan Rödiger, Michal Burdukiewicz, Andrej-Nikolai Spiess, Konstantin Blagodatskikh. Enabling reproducible real-time quantitative PCR research: the RDML package
4015 -- 4023Jana Ebler, Alexander Schönhuth, Tobias Marschall. Genotyping inversions and tandem duplications
4024 -- 4032Ilya Minkin, Son K. Pham, Paul Medvedev. TwoPaCo: an efficient algorithm to build the compacted de Bruijn graph from many complete genomes
4033 -- 4040Abhinav Nellore, Leonardo Collado-Torres, Andrew E. Jaffe, José Alquicira-Hernández, Christopher Wilks, Jacob Pritt, James Morton, Jeffrey T. Leek, Ben Langmead. Rail-RNA: scalable analysis of RNA-seq splicing and coverage
4041 -- 4048Snædís Kristmundsdóttir, Brynja D. Sigurpálsdóttir, Birte Kehr, Bjarni V. Halldórsson. popSTR: population-scale detection of STR variants
4049 -- 0José Juan Almagro Armenteros, Casper Kaae Sønderby, Søren Kaae Sønderby, Henrik Nielsen, Ole Winther. DeepLoc: prediction of protein subcellular localization using deep learning
4050 -- 0Riccardo Panero, Antonio Rinaldi, Domenico Memoli, Giovanni Nassa, Maria Ravo, Francesca Rizzo 0002, Roberta Tarallo, Luciano Milanesi, Alessandro Weisz, Giorgio Giurato. iSmaRT: a toolkit for a comprehensive analysis of small RNA-Seq data

Volume 33, Issue 23

3691 -- 3695Pedro Carmona-Saez, Nieves Varela, María José Luque, Daniel Toro-Domínguez, Jordi Martorell-Marugan, Marta E. Alarcón-Riquelme, Concepción Marañón. Metagene projection characterizes GEN2.2 and CAL-1 as relevant human plasmacytoid dendritic cell models
3696 -- 3700Trisevgeni Rapakoulia, Xin Gao, Yi Huang, Michiel J. L. de Hoon, Mariko Okada-Hatakeyama, Harukazu Suzuki, Erik Arner. Genome-scale regression analysis reveals a linear relationship for promoters and enhancers after combinatorial drug treatment
3701 -- 3708Linghao Shen, Jun Zhu, Shuo-Yen Robert Li, Xiaodan Fan. Detect differentially methylated regions using non-homogeneous hidden Markov model for methylation array data
3709 -- 3715Cuiping Pan, Gregory McInnes, Nicole Deflaux, Michael Snyder, Jonathan Bingham, Somalee Datta, Philip S. Tsao. Cloud-based interactive analytics for terabytes of genomic variants data
3716 -- 3725Meng Wang, Zhanglong Ji, Shuang Wang, Jihoon Kim, Hai Yang, Xiaoqian Jiang, Lucila Ohno-Machado. Mechanisms to protect the privacy of families when using the transmission disequilibrium test in genome-wide association studies
3726 -- 3732Pasi Rastas. Lep-MAP3: robust linkage mapping even for low-coverage whole genome sequencing data
3733 -- 3739Kai Wang. Conditional asymptotic inference for the kernel association test
3740 -- 3748André Müller, Christian Hundt 0002, Andreas Hildebrandt 0001, Thomas Hankeln, Bertil Schmidt. MetaCache: context-aware classification of metagenomic reads using minhashing
3749 -- 3757Jianwei Zhu, Haicang Zhang, Shuai Cheng Li, Chao Wang, Lupeng Kong, Shiwei Sun, Wei-Mou Zheng, Dongbo Bu. Improving protein fold recognition by extracting fold-specific features from predicted residue-residue contacts
3758 -- 3766Tushar Jain, Todd Boland, Asparouh Lilov, Irina Burnina, Michael Brown, Yingda Xu, Maximiliano Vásquez. Prediction of delayed retention of antibodies in hydrophobic interaction chromatography from sequence using machine learning
3767 -- 3775Alexis Delabrière, Ulli M. Hohenester, Benoit Colsch, Christophe Junot, François Fenaille, Etienne A. Thévenot. proFIA: a data preprocessing workflow for flow injection analysis coupled to high-resolution mass spectrometry
3776 -- 3783Zhenwen Dai, Mudassar Iqbal, Neil D. Lawrence, Magnus Rattray. Efficient inference for sparse latent variable models of transcriptional regulation
3784 -- 3792Chrysoula Zerva, Riza Batista-Navarro, Philip Day, Sophia Ananiadou. Using uncertainty to link and rank evidence from biomedical literature for model curation
3793 -- 3795Joshua S. Martin, Zheng Xu, Alex P. Reiner, Karen L. Mohlke, Patrick F. Sullivan, Bing Ren, Ming Hu, Yun Li. HUGIn: Hi-C Unifying Genomic Interrogator
3796 -- 3798Luis Vielva, María de Toro, Val F. Lanza, Fernando de la Cruz. PLACNETw: a web-based tool for plasmid reconstruction from bacterial genomes
3799 -- 3801Steven M. Foltz, Wen-Wei Liang, Mingchao Xie, Li Ding. MIRMMR: binary classification of microsatellite instability using methylation and mutations
3802 -- 3804Karol Pal, Vojtech Bystrý, Tomas Reigl, Martin Demko, Adam Krejci, Tasoula Touloumenidou, Evangelia Stalika, Boris Tichy, Paolo Ghia, Kostas Stamatopoulos, Sarka Pospisilova, Jitka Malcikova, Nikos Darzentas. GLASS: assisted and standardized assessment of gene variations from Sanger sequence trace data
3805 -- 3807Marco Enrico Piras, Luca Pireddu, Gianluigi Zanetti. wft4galaxy: a workflow testing tool for galaxy
3808 -- 3810João F. Matias Rodrigues, Thomas S. B. Schmidt, Janko Tackmann, Christian von Mering. MAPseq: highly efficient k-mer search with confidence estimates, for rRNA sequence analysis
3811 -- 3812Xuning Wang, Charles Tilford, Isaac Neuhaus, Gabe Mintier, Qi Guo, John N. Feder, Stefan Kirov. CRISPR-DAV: CRISPR NGS data analysis and visualization pipeline
3813 -- 3815Ignacio Faustino, Siewert J. Marrink. cgHeliParm: analysis of dsDNA helical parameters for coarse-grained MARTINI molecular dynamics simulations
3816 -- 3818Alexandre Borrel, Denis Fourches. RealityConvert: a tool for preparing 3D models of biochemical structures for augmented and virtual reality
3819 -- 3821Aleksandra M. Gierut, Wanda Niemyska, Pawel Dabrowski-Tumanski, Piotr Sulkowski, Joanna I. Sulkowska. PyLasso: a PyMOL plugin to identify lassos
3822 -- 3823Marcin Radom, Agnieszka Rybarczyk, Bartlomiej Szawulak, Hubert Andrzejewski, Piotr Chabelski, Adam Kozak, Piotr Formanowicz. Holmes: a graphical tool for development, simulation and analysis of Petri net based models of complex biological systems
3824 -- 3826Zachary Berndsen, Charles Bowman, Haerin Jang, Andrew B. Ward. EMHP: an accurate automated hole masking algorithm for single-particle cryo-EM image processing
3827 -- 3835Inuk Jung, Kyuri Jo, Hyejin Kang, Hongryul Ahn, Youngjae Yu, Sun Kim. TimesVector: a vectorized clustering approach to the analysis of time series transcriptome data from multiple phenotypes
3836 -- 3843Keisuke Yanagisawa, Shunta Komine, Shogo D. Suzuki, Masahito Ohue, Takashi Ishida, Yutaka Akiyama. Spresso: an ultrafast compound pre-screening method based on compound decomposition
3844 -- 3851Liang Zhao, Qingfeng Chen, Wencui Li, Peng Jiang, Limsoon Wong, Jinyan Li. MapReduce for accurate error correction of next-generation sequencing data
3852 -- 3860Yinglei Lai, Fanni Zhang, Tapan K. Nayak, Reza Modarres, Norman H. Lee, Timothy A. McCaffrey. An efficient concordant integrative analysis of multiple large-scale two-sample expression data sets
3861 -- 3870Yi Liu, Weiping Sun, Baozhen Shan, Kaizhong Zhang. DISC: DISulfide linkage Characterization from tandem mass spectra

Volume 33, Issue 22

3511 -- 3517José Carbonell-Caballero, Alicia Amadoz, Roberto Alonso, Marta R. Hidalgo, Cankut Çubuk, David V. Conesa, Antonio López-Quílez, Joaquín Dopazo. Reference genome assessment from a population scale perspective: an accurate profile of variability and noise
3518 -- 3523Wei Chen, Hui Yang, Peng-Mian Feng, Hui Ding, Hao Lin. iDNA4mC: identifying DNA N4-methylcytosine sites based on nucleotide chemical properties
3524 -- 3531Xiang Cheng, Shu-Guang Zhao, Wei-Zhong Lin, Xuan Xiao, Kuo-Chen Chou. pLoc-mAnimal: predict subcellular localization of animal proteins with both single and multiple sites
3532 -- 3537Jean-Michel Garant, Jean-Pierre Perreault, Michelle S. Scott. Motif independent identification of potential RNA G-quadruplexes by G4RNA screener
3538 -- 3548Feng Zhang, Yulan Lu, Sijia Yan, Qinghe Xing, Weidong Tian. SPRINT: an SNP-free toolkit for identifying RNA editing sites
3549 -- 3557Zixuan Cang, Guo-Wei Wei. Analysis and prediction of protein folding energy changes upon mutation by element specific persistent homology
3558 -- 3566Ashar Ahmad, Holger Fröhlich. Towards clinically more relevant dissection of patient heterogeneity via survival-based Bayesian clustering
3567 -- 3574Carl Brunius, Anders Pedersen, Daniel Malmodin, B. Göran Karlsson, Lars Andersson, Gunnel Tybring, Rikard Landberg. Prediction and modeling of pre-analytical sampling errors as a strategy to improve plasma NMR metabolomics data
3575 -- 3583Hanjun Dai, Ramzan Umarov, Hiroyuki Kuwahara, Yu Li, Le Song, Xin Gao. Sequence2Vec: a novel embedding approach for modeling transcription factor binding affinity landscape
3584 -- 3594V. M. Lourenço, P. C. Rodrigues, Ana M. Pires, Hans-Peter Piepho. A robust DF-REML framework for variance components estimation in genetic studies
3595 -- 3602Yao-Hwei Fang, Jie-Huei Wang, Chao A. Hsiung. TSGSIS: a high-dimensional grouped variable selection approach for detection of whole-genome SNP-SNP interactions
3603 -- 3609Siu Hung Joshua Chan, Jingyi Cai, Lin Wang, Margaret N. Simons-Senftle, Costas D. Maranas. Standardizing biomass reactions and ensuring complete mass balance in genome-scale metabolic models
3610 -- 3618Dana Ferranti, David Krane, David Craft. The value of prior knowledge in machine learning of complex network systems
3619 -- 3626Jonghwan Choi, Sanghyun Park, Youngmi Yoon, Jaegyoon Ahn. Improved prediction of breast cancer outcome by identifying heterogeneous biomarkers
3627 -- 3634Chao Pang, Fleur D. L. Kelpin, David van Enckevort, Niina Eklund, Kaisa Silander, Dennis Hendriksen, Mark de Haan, Jonathan Jetten, Tommy de Boer, Bart Charbon, Petr Holub, Hans L. Hillege, Morris A. Swertz. BiobankUniverse: automatic matchmaking between datasets for biobank data discovery and integration
3635 -- 3637Osamu Nishimura, Yuichiro Hara, Shigehiro Kuraku. gVolante for standardizing completeness assessment of genome and transcriptome assemblies
3638 -- 3641Matthew D. Whiteside, Victor P. J. Gannon, Chad R. Laing. Phylotyper: in silico predictor of gene subtypes
3642 -- 3644Yuanyan Xiong, Xiaowei Xie, Yanzhi Wang, Wenbin Ma, Puping Liang, Songyang Zhou, Zhiming Dai. pgRNAFinder: a web-based tool to design distance independent paired-gRNA
3645 -- 3647Omar Wagih. ggseqlogo: a versatile R package for drawing sequence logos
3648 -- 3651Ravi José Tristão Ramos, Allan Cézar de Azevedo Martins, Gabrielle da Silva Delgado, Crina-Maria Ionescu, Turán Peter Ürményi, Rosane Silva, Jaroslav Koca. CrocoBLAST: Running BLAST efficiently in the age of next-generation sequencing
3652 -- 3654Sean La, Ehsan Haghshenas, Cédric Chauve. LRCstats, a tool for evaluating long reads correction methods
3655 -- 3657Joan Segura, Rubén Sánchez García, Marta Martínez, Jesús Cuenca Alba, Daniel Tabas-Madrid, Carlos Oscar Sánchez Sorzano, José María Carazo. 3DBIONOTES v2.0: a web server for the automatic annotation of macromolecular structures
3658 -- 3660David Lagorce, Lina Bouslama, Jérôme Bécot, Maria A. Miteva, Bruno O. Villoutreix. FAF-Drugs4: free ADME-tox filtering computations for chemical biology and early stages drug discovery
3661 -- 3663Lin Li, Zhe Jia, Yunhui Peng, Arghya Chakravorty, Lexuan Sun, Emil Alexov. DelPhiForce web server: electrostatic forces and energy calculations and visualization
3664 -- 3666Chia-Lang Hsu, Jiankai Wang, Pei-Chun Lu, Hsuan-Cheng Huang, Hsueh-Fen Juan. DynaPho: a web platform for inferring the dynamics of time-series phosphoproteomics
3667 -- 3669Marek Kochanczyk, William S. Hlavacek, Tomasz Lipniacki. SPATKIN: a simulator for rule-based modeling of biomolecular site dynamics on surfaces
3670 -- 3672Glyn Bradley, Steven J. Barrett. CausalR: extracting mechanistic sense from genome scale data
3673 -- 3675Colin W. Combe, Marine Sivade, Henning Hermjakob, Joshua Heimbach, Birgit H. M. Meldal, Gos Micklem, Sandra E. Orchard, Juri Rappsilber. ComplexViewer: visualization of curated macromolecular complexes
3676 -- 3678Alessandro Pietrelli, Luca Valenti. myVCF: a desktop application for high-throughput mutations data management
3679 -- 3681Daniel Domingo-Fernández, Alpha Tom Kodamullil, Anandhi Iyappan, Mufassra Naz, Mohammad Asif Emon, Tamara Raschka, Reagon Karki, Stephan Springstubbe, Christian Ebeling, Martin Hofmann-Apitius. Multimodal mechanistic signatures for neurodegenerative diseases (NeuroMMSig): a web server for mechanism enrichment
3682 -- 3684Erzsébet Fichó, István Reményi, István Simon, Bálint Mészáros. MFIB: a repository of protein complexes with mutual folding induced by binding
3685 -- 3690Vanessa Isabell Jurtz, Alexander Rosenberg Johansen, Morten Nielsen, José Juan Almagro Armenteros, Henrik Nielsen, Casper Kaae Sønderby, Ole Winther, Søren Kaae Sønderby. An introduction to deep learning on biological sequence data: examples and solutions

Volume 33, Issue 21

3331 -- 3339Emmanuel Noutahi, Virginie Calderon, Mathieu Blanchette, B. Franz Lang, Nadia El-Mabrouk. CoreTracker: accurate codon reassignment prediction, applied to mitochondrial genomes
3340 -- 3347Zhiqun Xie, Haixu Tang. ISEScan: automated identification of insertion sequence elements in prokaryotic genomes
3348 -- 3354Yuchao Xia, Yun Liu, Minghua Deng, Ruibin Xi. SVmine improves structural variation detection by integrative mining of predictions from multiple algorithms
3355 -- 3363Mohammed Alser, Hasan Hassan, Hongyi Xin, Oguz Ergin, Onur Mutlu, Can Alkan. GateKeeper: a new hardware architecture for accelerating pre-alignment in DNA short read mapping
3364 -- 3372Yuansheng Liu, Hui Peng, Limsoon Wong, Jinyan Li. High-speed and high-ratio referential genome compression
3373 -- 3379Jirí Hon, Tomás Martínek, Jaroslav Zendulka, Matej Lexa. pqsfinder: an exhaustive and imperfection-tolerant search tool for potential quadruplex-forming sequences in R
3380 -- 3386Hirak Sarkar, Robert Patro. Quark enables semi-reference-based compression of RNA-seq data
3387 -- 3395José Juan Almagro Armenteros, Casper Kaae Sønderby, Søren Kaae Sønderby, Henrik Nielsen, Ole Winther. DeepLoc: prediction of protein subcellular localization using deep learning
3396 -- 3404Jan P. Meier-Kolthoff, Markus Göker. VICTOR: genome-based phylogeny and classification of prokaryotic viruses
3405 -- 3414Pawel P. Wozniak, Bogumil Konopka, J. Xu, Gert Vriend, Malgorzata Kotulska. Forecasting residue-residue contact prediction accuracy
3415 -- 3422Fabrizio Pucci, Jean Marc Kwasigroch, Marianne Rooman. SCooP: an accurate and fast predictor of protein stability curves as a function of temperature
3423 -- 3430Huamin Li, Uri Shaham, Kelly P. Stanton, Yi Yao, Ruth R. Montgomery, Yuval Kluger. Gating mass cytometry data by deep learning
3431 -- 3436Sébastien De Landtsheer, Panuwat Trairatphisan, Philippe Lucarelli, Thomas Sauter. FALCON: a toolbox for the fast contextualization of logical networks
3437 -- 3444Giorgos Minas, Dafyd J. Jenkins, David A. Rand, Bärbel Finkenstädt. Inferring transcriptional logic from multiple dynamic experiments
3445 -- 3453Satya Swarup Samal, Ovidiu Radulescu, Andreas Weber 0004, Holger Fröhlich. Linking metabolic network features to phenotypes using sparse group lasso
3454 -- 3460Sylvain Poux, Cecilia N. Arighi, Michele Magrane, Alex Bateman, Chih-Hsuan Wei, Zhiyong Lu, Emmanuel Boutet, Hema Bye-A-Jee, Maria Livia Famiglietti, Bernd Roechert, The UniProt Consortium. On expert curation and scalability: UniProtKB/Swiss-Prot as a case study
3461 -- 3467Konstantinos Sidiropoulos, Guilherme Viteri, Cristoffer Sevilla, Steven Jupe, Marissa Webber, Marija Orlic-Milacic, Bijay Jassal, Bruce May, Veronica Shamovsky, Corina Duenas, Karen Rothfels, Lisa Matthews, Heeyeon Song, Lincoln Stein, Robin Haw, Peter D'Eustachio, Peipei Ping, Henning Hermjakob, Antonio Fabregat. Reactome enhanced pathway visualization
3468 -- 3470Mete Akgün, Hüseyin Demirci. VCF-Explorer: filtering and analysing whole genome VCF files
3471 -- 3472Mathieu Schaeffer, Alain Gateau, Daniel Teixeira, Pierre-André Michel, Monique Zahn-Zabal, Lydie Lane. The neXtProt peptide uniqueness checker: a tool for the proteomics community
3473 -- 3476Junjie Chen, Mingyue Guo, Shumin Li, Bin Liu. ProtDec-LTR2.0: an improved method for protein remote homology detection by combining pseudo protein and supervised Learning to Rank
3477 -- 3479Jun Ding, Ziv Bar-Joseph. MethRaFo: MeDIP-seq methylation estimate using a Random Forest Regressor
3480 -- 3481Jinling Shang, Xi Dai, Yecheng Li, Marco Pistolozzi, Ling Wang. HybridSim-VS: a web server for large-scale ligand-based virtual screening using hybrid similarity recognition techniques
3482 -- 3485Anna Laddach, Mathias Gautel, Franca Fraternali. TITINdb - a computational tool to assess titin's role as a disease gene
3486 -- 3488Beate Vieth, Christoph Ziegenhain, Swati Parekh, Wolfgang Enard, Ines Hellmann. powsimR: power analysis for bulk and single cell RNA-seq experiments
3489 -- 3491Danica Wiredja, Mehmet Koyutürk, Mark R. Chance. The KSEA App: a web-based tool for kinase activity inference from quantitative phosphoproteomics
3492 -- 3494Leonard A. Harris, Marco S. Nobile, James C. Pino, Alexander L. R. Lubbock, Daniela Besozzi, Giancarlo Mauri, Paolo Cazzaniga, Carlos F. Lopez. GPU-powered model analysis with PySB/cupSODA
3495 -- 3496Kun Sun, Fiona F. M. Lun, Peiyong Jiang, Hao Sun 0001. BSviewer: a genotype-preserving, nucleotide-level visualizer for bisulfite sequencing data
3497 -- 3499Ahmed Allam, Michael Krauthammer. PySeqLab: an open source Python package for sequence labeling and segmentation
3500 -- 3501Katja Koeppen, Bruce A. Stanton, Thomas H. Hampton. ScanGEO: parallel mining of high-throughput gene expression data
3502 -- 3504Ian H. Holmes, Christopher J. Mungall. BioMake: a GNU make-compatible utility for declarative workflow management
3505 -- 3507Meng-Pin Weng, Ben-Yang Liao. modPhEA: model organism Phenotype Enrichment Analysis of eukaryotic gene sets
3508 -- 3510Rory Nolan, Luis A. J. Alvarez, Jonathan Elegheert, Maro Iliopoulou, G. Maria Jakobsdottir, Marina Rodriguez-Muñoz, A. Radu Aricescu, Sergi Padilla-Parra. nandb - number and brightness in R with a novel automatic detrending algorithm

Volume 33, Issue 20

3151 -- 3157Yu-Jia Shiah, Michael Fraser, Robert G. Bristow, Paul C. Boutros. Comparison of pre-processing methods for Infinium HumanMethylation450 BeadChip array
3158 -- 3165Elena D. Stavrovskaya, Tejasvi Niranjan, Elana J. Fertig, Sarah J. Wheelan, Alexander V. Favorov, Andrey A. Mironov. StereoGene: rapid estimation of genome-wide correlation of continuous or interval feature data
3166 -- 3172Qing Zhang, Xiaodan Fan, Yejun Wang, Ming-an Sun, Jianlin Shao, Dianjing Guo. BPP: a sequence-based algorithm for branch point prediction
3173 -- 3180Moritz Hess, Stefan Lenz, Tamara J. Blätte, Lars Bullinger, Harald Binder. Partitioned learning of deep Boltzmann machines for SNP data
3181 -- 3187Martin D. Muggli, Alexander Bowe, Noelle R. Noyes, Paul S. Morley, Keith E. Belk, Robert Raymond, Travis Gagie, Simon J. Puglisi, Christina Boucher. Succinct colored de Bruijn graphs
3188 -- 3194Antoine Recanati, Thomas Brüls, Alexandre d'Aspremont. A spectral algorithm for fast de novo layout of uncorrected long nanopore reads
3195 -- 3201Li Huang, Xianhong Li, Pengfei Guo, Yuhua Yao, Bo Liao, Weiwei Zhang, Fayou Wang, Jiasheng Yang, Yulong Zhao, Hailiang Sun, Pingan He, Jialiang Yang. Matrix completion with side information and its applications in predicting the antigenicity of influenza viruses
3202 -- 3210Marc G. Chevrette, Fabian Aicheler, Oliver Kohlbacher, Cameron R. Currie, Marnix H. Medema. SANDPUMA: ensemble predictions of nonribosomal peptide chemistry reveal biosynthetic diversity across Actinobacteria
3211 -- 3219Nikolaos K. Chlis, F. Alexander Wolf, Fabian J. Theis. Model-based branching point detection in single-cell data by K-branches clustering
3220 -- 3227Martin Schäfer, Hans-Ulrich Klein, Holger Schwender. Integrative analysis of multiple genomic variables using a hierarchical Bayesian model
3228 -- 3234Attila Csala, Frans Voorbraak, Aeilko H. Zwinderman, Michel H. Hof. Sparse redundancy analysis of high-dimensional genetic and genomic data
3235 -- 3242Arief Gusnanto, John Paul Gosling, Christopher Pope. Identification of transcript regulatory patterns in cell differentiation
3243 -- 3249Paul Vauterin, Ben Jeffery, Alistair Miles, Roberto Amato, Lee Hart, Ian Wright, Dominic Kwiatkowski. Panoptes: web-based exploration of large scale genome variation data
3250 -- 3257Xiaohui Yao, Jingwen Yan, Kefei Liu, Sungeun Kim, Kwangsik Nho, Shannon L. Risacher, Casey S. Greene, Jason H. Moore, Andrew J. Saykin, Li Shen 0001. Tissue-specific network-based genome wide study of amygdala imaging phenotypes to identify functional interaction modules
3258 -- 3267Iurie Caraus, Bogdan Mazoure, Robert Nadon, Vladimir Makarenkov. Detecting and removing multiplicative spatial bias in high-throughput screening technologies
3268 -- 3275Yu He, Ting Wang. EpiCompare: an online tool to define and explore genomic regions with tissue or cell type-specific epigenomic features
3276 -- 3282Xian Zeng, Lin Tao, Peng Zhang, Chu Qin, Shangying Chen, Weidong He, Ying Tan, Hong-Xia Liu, Sheng-Yong Yang, Zhe Chen, Yu Yang Jiang, Yu Zong Chen. HEROD: a human ethnic and regional specific omics database
3283 -- 3285Ludovic Mallet, Tristan Bitard-Feildel, Franck Cerutti, Hélène Chiapello. PhylOligo: a package to identify contaminant or untargeted organism sequences in genome assemblies
3286 -- 3288Li Yao, Heming Wang, Yuanyuan Song, Guangchao Sui. BioQueue: a novel pipeline framework to accelerate bioinformatics analysis
3289 -- 3291Changlin Wan, Jianing Gao, Huan Zhang, Xiaohua Jiang, Qiguang Zang, Rongjun Ban, Yuanwei Zhang, Qinghua Shi. CPSS 2.0: a computational platform update for the analysis of small RNA sequencing data
3292 -- 3295Philipp C. Münch, Bärbel Stecher, Alice C. McHardy. EDEN: evolutionary dynamics within environments
3296 -- 3298Minji Kim, Yeonsung Kim, Lei Qian, Jun S. Song. TeachEnG: a Teaching Engine for Genomics
3299 -- 3301Kathryn A. Porter, Bing Xia, Dmitri Beglov, Tanggis Bohnuud, Nawsad Alam, Ora Schueler-Furman, Dima Kozakov. ClusPro PeptiDock: efficient global docking of peptide recognition motifs using FFT
3302 -- 3304Igor Mandric, Yvette Temate-Tiagueu, Tatiana Shcheglova, Sahar Al Seesi, Alex Zelikovsky, Ion I. Mandoiu. Fast bootstrapping-based estimation of confidence intervals of expression levels and differential expression from RNA-Seq data
3305 -- 3307Alexey Uvarovskii, Christoph Dieterich. pulseR: Versatile computational analysis of RNA turnover from metabolic labeling experiments
3308 -- 3310Wenbin Guo, Cristiane P. G. Calixto, John W. S. Brown, Runxuan Zhang. TSIS: an R package to infer alternative splicing isoform switches for time-series data
3311 -- 3313Michael F. Lawrence, Robert Gentleman. VariantTools: an extensible framework for developing and testing variant callers
3314 -- 3316Xianwen Meng, Qi Chen, Peijing Zhang, Ming Chen. CircPro: an integrated tool for the identification of circRNAs with protein-coding potential
3317 -- 3319Sajid Mughal, Ismail Moghul, Jing Yu, Ukirdc, Tristan Clark, David S. Gregory, Nikolas Pontikos. Pheno4J: a gene to phenotype graph database
3320 -- 3322Sam Cooper, Alexis R. Barr, Robert Glen, Chris Bakal. NucliTrack: an integrated nuclei tracking application
3323 -- 3330Mikhail G. Dozmorov. Epigenomic annotation-based interpretation of genomic data: from enrichment analysis to machine learning

Volume 33, Issue 2

151 -- 154Ahmed Arslan, Vera van Noort. Evolutionary conservation of Ebola virus proteins predicts important functions at residue level
155 -- 160Niko Popitsch, WGS500 Consortium, Anna Schuh, Jenny C. Taylor. ReliableGenome: annotation of genomic regions with high/low variant calling concordance
161 -- 168Xiao Wang, Jinghua Gu, Leena Hilakivi-Clarke, Robert Clarke, Jianhua Xuan. DM-BLD: differential methylation detection using a hierarchical Bayesian model exploiting local dependency
169 -- 176Junwei Luo, Jianxin Wang, Zhen Zhang, Min Li, Fang-Xiang Wu. BOSS: a novel scaffolding algorithm based on an optimized scaffold graph
177 -- 183Xi Chen, Xu Shi, Leena Hilakivi-Clarke, Ayesha N. Shajahan-Haq, Robert Clarke, Jianhua Xuan. PSSV: a novel pattern-based probabilistic approach for somatic structural variation identification
184 -- 191Ying Liang, Kunlong Qiu, Bo Liao, Wen Zhu, Xuanlin Huang, Lin Li, Xiangtao Chen, Keqin Li. Seeksv: an accurate tool for somatic structural variation and virus integration detection
192 -- 201Bo Liu, Yan Gao, Yadong Wang. LAMSA: fast split read alignment with long approximate matches
202 -- 209Yuki Kato, Tomoya Mori, Kengo Sato, Shingo Maegawa, Hiroshi Hosokawa, Tatsuya Akutsu. An accessibility-incorporated method for accurate prediction of RNA-RNA interactions from sequence data
210 -- 218Irene Rodríguez-Luján, Jeff Hasty, Ramón Huerta. FBB: a fast Bayesian-bound tool to calibrate RNA-seq aligners
219 -- 226M. Altenbuchinger, T. Rehberg, H. U. Zacharias, F. Stämmler, K. Dettmer, D. Weber, A. Hiergeist, A. Gessner, E. Holler, Peter J. Oefner, R. Spang. Reference point insensitive molecular data analysis
227 -- 234Joseph Azofeifa, Robin D. Dowell. A generative model for the behavior of RNA polymerase
235 -- 242Chunxuan Shao, Thomas Höfer. Robust classification of single-cell transcriptome data by nonnegative matrix factorization
243 -- 247Wenyu Wang, Jingcan Hao, Shuyu Zheng, Qianrui Fan, Awen He, Yan Wen, Xiong Guo, Cuiyan Wu, Sen Wang, Tielin Yang, Hui Shen, Xiangding Chen, Qing Tian, Lijun Tan, Hong-Wen Deng, Feng Zhang. Tissue-specific pathway association analysis using genome-wide association study summaries
248 -- 255Gleb Kichaev, Megan Roytman, Ruth Johnson, Eleazar Eskin, Sara Lindström, Peter Kraft, Bogdan Pasaniuc. Improved methods for multi-trait fine mapping of pleiotropic risk loci
256 -- 265Yan Yan, Shangzhao Qiu, Zhuxuan Jin, Sihong Gong, Yun Bai, Jianwei Lu, Tianwei Yu. Detecting subnetwork-level dynamic correlations
266 -- 271Muhammad Shoaib, Adnan Ahmad Ansari, Sung-Min Ahn. cMapper: gene-centric connectivity mapper for EBI-RDF platform
272 -- 279Jie Zheng, Mesut A. Erzurumluoglu, Benjamin L. Elsworth, John P. Kemp, Laurence Howe, Philip C. Haycock, Gibran Hemani, Katherine Tansey, Charles Laurin, Early Genetics, Lifecourse Epidemiology (EAGLE) Eczema Consortium, Beate St. Pourcain, Nicole M. Warrington, Hilary K. Finucane, Alkes L. Price, Brendan K. Bulik-Sullivan, Verneri Anttila, Lavinia Paternoster, Tom R. Gaunt, David M. Evans, Benjamin M. Neale. LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis
280 -- 282Sergii Ivakhno, Camilla Colombo, Stephen Tanner, Philip Tedder, Stefano Berri, Anthony J. Cox. tHapMix: simulating tumour samples through haplotype mixtures
283 -- 285Val F. Lanza, Fernando Baquero, Fernando de la Cruz, Teresa M. Coque. AcCNET (Accessory Genome Constellation Network): comparative genomics software for accessory genome analysis using bipartite networks
286 -- 288Jeongbin Park, Kayeong Lim, Jin-Soo Kim, Sangsu Bae. Cas-analyzer: an online tool for assessing genome editing results using NGS data
289 -- 291Vladimir Perovic, Neven Sumonja, Branislava Gemovic, Eneda Toska, Stefan G. Roberts, Nevena Veljkovic. TRI_tool: a web-tool for prediction of protein-protein interactions in human transcriptional regulation
292 -- 293Aaron M. Rosenfeld, Wenzhao Meng, Eline T. Luning Prak, Uri Hershberg. ImmuneDB: a system for the analysis and exploration of high-throughput adaptive immune receptor sequencing data
294 -- 296Rasool Tahmasbi, Matthew C. Keller. GeneEvolve: a fast and memory efficient forward-time simulator of realistic whole-genome sequence and SNP data
297 -- 299Hasan Baig, Jan Madsen. D-VASim: an interactive virtual laboratory environment for the simulation and analysis of genetic circuits
300 -- 302Ruggero Ferrazza, Julian L. Griffin, Graziano Guella, Pietro Franceschi. IsotopicLabelling: an R package for the analysis of MS isotopic patterns of labelled analytes
303 -- 305Max Klein, Rati Sharma, Chris H. Bohrer, Cameron M. Avelis, Elijah Roberts. Biospark: scalable analysis of large numerical datasets from biological simulations and experiments using Hadoop and Spark
306 -- 308Matthew Norris, Chun Kit Kwok, Jitender Cheema, Matthew Hartley, Richard J. Morris, Sharon Aviran, Yiliang Ding. FoldAtlas: a repository for genome-wide RNA structure probing data
309 -- 0Andy L. Olivares, Miguel Ángel González Ballester, Jérôme Noailly. Virtual exploration of early stage atherosclerosis

Volume 33, Issue 19

2971 -- 2976Minh N. Nguyen, Mohan R. Pradhan, Chandra Verma, Pingyu Zhong. The interfacial character of antibody paratopes: analysis of antibody-antigen structures
2977 -- 2985Sylvain Mareschal, Philippe Ruminy, Marion Alcantara, Céline Villenet, Martin Figeac, Sydney Dubois, Philippe Bertrand, Abdelilah Bouzelfen, Pierre-Julien Viailly, Dominique Penther, Hervé Tilly, Christian Bastard, Fabrice Jardin. Application of the cghRA framework to the genomic characterization of Diffuse Large B-Cell Lymphoma
2986 -- 2994Milos Pavlovic, Pradipta Ray, Kristina Pavlovic, Aaron Kotamarti, Min Chen, Michael Q. Zhang. DIRECTION: a machine learning framework for predicting and characterizing DNA methylation and hydroxymethylation in mammalian genomes
2995 -- 3002Jacquiline W. Mugo, Ephifania Geza, Joel Defo, Samar S. M. Elsheikh, Gaston K. Mazandu, Nicola J. Mulder, Emile R. Chimusa. A multi-scenario genome-wide medical population genetics simulation framework
3003 -- 3010Wenxiu Ma, Lin Yang, Remo Rohs, William Stafford Noble. DNA sequence+shape kernel enables alignment-free modeling of transcription factor binding
3011 -- 3017Cristian Zambrano-Vega, Antonio J. Nebro, José García-Nieto, José Francisco Aldana Montes. M2Align: parallel multiple sequence alignment with a multi-objective metaheuristic
3018 -- 3027Hao Peng, Yifan Yang, Shandian Zhe, Jian Wang, Michael Gribskov, Yuan Qi. DEIsoM: a hierarchical Bayesian model for identifying differentially expressed isoforms using biological replicates
3028 -- 3035Ka Chun Wong. MotifHyades: expectation maximization for de novo DNA motif pair discovery on paired sequences
3036 -- 3042J. Jiménez, Stefan Doerr, G. Martínez-Rosell, A. S. Rose, Gianni De Fabritiis. DeepSite: protein-binding site predictor using 3D-convolutional neural networks
3043 -- 3050Christopher W. Wood, Jack W. Heal, Andrew R. Thomson, Gail J. Bartlett, Amaurys Ávila Ibarra, R. Leo Brady, Richard B. Sessions, Derek N. Woolfson. ISAMBARD: an open-source computational environment for biomolecular analysis, modelling and design
3051 -- 3057Sang-Jun Park, Jumin Lee, Dhilon S. Patel, Hongjing Ma, Hui Sun Lee, Sunhwan Jo, Wonpil Im. Glycan Reader is improved to recognize most sugar types and chemical modifications in the Protein Data Bank
3058 -- 3064Dimitrios V. Vavoulis, Jenny C. Taylor, Anna Schuh. Hierarchical probabilistic models for multiple gene/variant associations based on next-generation sequencing data
3065 -- 3071Alice Madonia, Cristiano Melchiorri, Simone Bonamano, Marco Marcelli, Chiara Bulfon, Filippo Castiglione, Marco Galeotti, Donatella Volpatti, Francesco Mosca, Pietro-Giorgio Tiscar, Nicla Romano. Computational modeling of immune system of the fish for a more effective vaccination in aquaculture
3072 -- 3079Christoph Schmal, Jihwan Myung, Hanspeter Herzel, Grigory V. Bordyugov. Moran's I quantifies spatio-temporal pattern formation in neural imaging data
3080 -- 3087Jiadong Ji, Di He, Yang Feng, Yong He, Fuzhong Xue, Lei Xie. JDINAC: joint density-based non-parametric differential interaction network analysis and classification using high-dimensional sparse omics data
3088 -- 3090Bernat Gel, Eduard Serra. karyoploteR: an R/Bioconductor package to plot customizable genomes displaying arbitrary data
3091 -- 3093Rallis Karamichalis, Lila Kari. MoDMaps3D: an interactive webtool for the quantification and 3D visualization of interrelationships in a dataset of DNA sequences
3094 -- 3095Giorgio Gonnella, Stefan Kurtz. GfaPy: a flexible and extensible software library for handling sequence graphs in Python
3096 -- 3097William L. Miller, W. David Walter. CWDPRNP: a tool for cervid prion sequence analysis in program R
3098 -- 3100Max Hebditch, M. Alejandro Carballo-Amador, Spyros Charonis, Robin Curtis, Jim Warwicker. Protein-Sol: a web tool for predicting protein solubility from sequence
3101 -- 3103Andrew Low, Nicolas Rodrigue, Alex Wong. COMPASS: the COMPletely Arbitrary Sequence Simulator
3104 -- 3106Alexandros Armaos, Davide Cirillo, Gian Gaetano Tartaglia. omiXcore: a web server for prediction of protein interactions with large RNA
3107 -- 3109Yuxuan Yuan, Philipp E. Bayer, Huey-Tyng Lee, David Edwards. runBNG: a software package for BioNano genomic analysis on the command line
3110 -- 3112Preeti Bais, Sandeep Namburi, Daniel M. Gatti, Xinyu Zhang, Jeffrey H. Chuang. CloudNeo: a cloud pipeline for identifying patient-specific tumor neoantigens
3113 -- 3114Clovis Galiez, Matthias Siebert, François Enault, Jonathan Vincent, Johannes Söding. WIsH: who is the host? Predicting prokaryotic hosts from metagenomic phage contigs
3115 -- 3116Jochen Kruppa, Erhard van der Vries, Wendy K. Jo, Alexander Postel, Paul Becher, Albert Osterhaus, Klaus Jung. kmerPyramid: an interactive visualization tool for nucleobase and k-mer frequencies
3117 -- 3120Jean-Pierre Séhi Glouzon, Jean-Pierre Perreault, Shengrui Wang. Structurexplor: a platform for the exploration of structural features of RNA secondary structures
3121 -- 3122Matthew A. Wyczalkowski, Kristine M. Wylie, Song Cao, Michael D. McLellan, Jennifer Flynn, Mo Huang, Kai Ye, Xian Fan, Ken Chen, Michael C. Wendl, Li Ding. BreakPoint Surveyor: a pipeline for structural variant visualization
3123 -- 3125Vincent Gardeux, Fabrice P. A. David, Adrian Shajkofci, Petra C. Schwalie, Bart Deplancke. ASAP: a web-based platform for the analysis and interactive visualization of single-cell RNA-seq data
3126 -- 3128Jason T. Serviss, Jesper Gådin, Per Eriksson, Lasse Folkersen, Dan Grandér. ClusterSignificance: a bioconductor package facilitating statistical analysis of class cluster separations in dimensionality reduced data
3129 -- 3130Ilya Y. Zhbannikov, Konstantin G. Arbeev, Anatoliy I. Yashin. rqt: an R package for gene-level meta-analysis
3131 -- 3133Taosheng Xu, Thuc Duy Le, Lin Liu 0003, Ning Su, Rujing Wang, Bing-Yu Sun, Antonio Colaprico, Gianluca Bontempi, Jiuyong Li. CancerSubtypes: an R/Bioconductor package for molecular cancer subtype identification, validation and visualization
3134 -- 3136Aditya Bharadwaj, Divit P. Singh, Anna M. Ritz, Allison N. Tegge, Christopher L. Poirel, Pavel K. Brazhnik, Neil Adames, Kurt Luther, Shiv D. Kale, Jean Peccoud, John J. Tyson, T. M. Murali. GraphSpace: stimulating interdisciplinary collaborations in network biology
3137 -- 3139Joseph W. Brown, Megan Pirrung, Lee Ann McCue. FQC Dashboard: integrates FastQC results into a web-based, interactive, and extensible FASTQ quality control tool
3140 -- 3141Elias Tappeiner, Francesca Finotello, Pornpimol Charoentong, Clemens Mayer, Dietmar Rieder, Zlatko Trajanoski. TIminer: NGS data mining pipeline for cancer immunology and immunotherapy
3142 -- 3144Kylie A. Bemis, Olga Vitek. matter: an R package for rapid prototyping with larger-than-memory datasets on disk
3145 -- 3147Chris Churas, Alex J. Perez, Hiroyuki Hakozaki, Willy Wong, David Lee, Steven Peltier, Mark H. Ellisman. Probability Map Viewer: near real-time probability map generator of serial block electron microscopy collections
3148 -- 3150Emil Jørsboe, Kristian Hanghøj, Anders Albrechtsen. fastNGSadmix: admixture proportions and principal component analysis of a single NGS sample

Volume 33, Issue 18

2791 -- 2798Nora Rieber, Regina Bohnert, Ulrike Ziehm, Gunther Jansen. Reliability of algorithmic somatic copy number alteration detection from targeted capture data
2799 -- 2807Zaixiang Tang, Yueping Shen, Xinyan Zhang, Nengjun Yi. The spike-and-slab lasso Cox model for survival prediction and associated genes detection
2808 -- 2817Ferdinando Montecuollo, Giovannni Schmid, Roberto Tagliaferri. E2FM: an encrypted and compressed full-text index for collections of genomic sequences
2818 -- 2828Burçak Otlu, Can Firtina, Sündüz Keles, Oznur Tastan. GLANET: genomic loci annotation and enrichment tool
2829 -- 2836Xiong Li. A fast and exhaustive method for heterogeneity and epistasis analysis based on multi-objective optimization
2837 -- 2841Loris Nanni, Sheryl Brahnam. Multi-label classifier based on histogram of gradients for predicting the anatomical therapeutic chemical class/classes of a given compound
2842 -- 2849Rhys Heffernan, Yuedong Yang, Kuldip K. Paliwal, Yaoqi Zhou. Capturing non-local interactions by long short-term memory bidirectional recurrent neural networks for improving prediction of protein secondary structure, backbone angles, contact numbers and solvent accessibility
2850 -- 2858Stefan Hammer, Birgit Tschiatschek, Christoph Flamm, Ivo L. Hofacker, Sven Findeiß. RNAblueprint: flexible multiple target nucleic acid sequence design
2859 -- 2866Mirco Michel, Marcin J. Skwark, David Menéndez Hurtado, Magnus Ekeberg, Arne Elofsson. Predicting accurate contacts in thousands of Pfam domain families using PconsC3
2867 -- 2872Bahjat F. Qaqish, Jonathon J. O'Brien, Jonathan C. Hibbard, Katie J. Clowers. Accelerating high-dimensional clustering with lossless data reduction
2873 -- 2881Jian Xiao, Hongyuan Cao, Jun Chen. False discovery rate control incorporating phylogenetic tree increases detection power in microbiome-wide multiple testing
2882 -- 2889Mingwei Dai, Jingsi Ming, Mingxuan Cai, Jin Liu, Can Yang, Xiang Wan, ZongBen Xu. IGESS: a statistical approach to integrating individual-level genotype data and summary statistics in genome-wide association studies
2890 -- 2896Nicolas Städler, Frank Dondelinger, Steven M. Hill, Rehan Akbani, Yiling Lu, Gordon B. Mills, Sach Mukherjee. Molecular heterogeneity at the network level: high-dimensional testing, clustering and a TCGA case study
2897 -- 2905Kristen A. Severson, Brinda Monian, J. Christopher Love, Richard D. Braatz. A method for learning a sparse classifier in the presence of missing data for high-dimensional biological datasets
2906 -- 2913Trang T. Le, W. Kyle Simmons, Masaya Misaki, Jerzy Bodurka, Bill C. White, Jonathan Savitz, Brett A. McKinney. Differential privacy-based evaporative cooling feature selection and classification with relief-F and random forests
2914 -- 2923Matthew Bernstein, AnHai Doan, Colin N. Dewey. MetaSRA: normalized human sample-specific metadata for the Sequence Read Archive
2924 -- 2929Nili Tickotsky, Tal Sagiv, Jaime Prilusky, Eric Shifrut, Nir Friedman. McPAS-TCR: a manually curated catalogue of pathology-associated T cell receptor sequences
2930 -- 2932Zhicheng Ji, Weiqiang Zhou, Hongkai Ji. Single-cell regulome data analysis by SCRAT
2933 -- 2935Alden King-Yung Leung, Nana Jin, Kevin Y. Yip, Ting-Fung Chan. OMTools: a software package for visualizing and processing optical mapping data
2936 -- 2937Byoungnam Min, Igor V. Grigoriev, In-Geol Choi. FunGAP: Fungal Genome Annotation Pipeline using evidence-based gene model evaluation
2938 -- 2940Jake R. Conway, Alexander Lex, Nils Gehlenborg. UpSetR: an R package for the visualization of intersecting sets and their properties
2941 -- 2942Johannes T. Roehr, Christoph Dieterich, Knut Reinert. Flexbar 3.0 - SIMD and multicore parallelization
2943 -- 2945Kamil Jan Cygan, Clayton Hendrick Sanford, William G. Fairbrother. Spliceman2: a computational web server that predicts defects in pre-mRNA splicing
2946 -- 2947Lukasz Kreft, Alexander Botzki, Frederik Coppens, Klaas Vandepoele, Michiel Van Bel. PhyD3: a phylogenetic tree viewer with extended phyloXML support for functional genomics data visualization
2948 -- 2950José Manuel Abuín, Tomás F. Pena, Juan Carlos Pichel. PASTASpark: multiple sequence alignment meets Big Data
2951 -- 2953Jiannong Li, Inna Smalley, Michael J. Schell, Keiran S. M. Smalley, Y. Ann Chen. SinCHet: a MATLAB toolbox for single cell heterogeneity analysis in cancer
2954 -- 2956Stian Lågstad, Sen Zhao, Andreas M. Hoff, Bjarne Johannessen, Ole Christian Lingjærde, Rolf I. Skotheim. chimeraviz: a tool for visualizing chimeric RNA
2957 -- 2959Jinghua Gu, Xuan Wang, Jinyan Chan, Nicole E. Baldwin, Jacob A. Turner. Phantom: investigating heterogeneous gene sets in time-course data
2960 -- 2962Christian Scheeder, Florian Heigwer, Michael Boutros. HTSvis: a web app for exploratory data analysis and visualization of arrayed high-throughput screens
2963 -- 2965Hyun-hwan Jeong, Seon-Young Kim, Maxime W. C. Rousseaux, Huda Y. Zoghbi, Zhandong Liu. CRISPRcloud: a secure cloud-based pipeline for CRISPR pooled screen deconvolution
2966 -- 2967Atis Elsts, Agris Pentjuss, Egils Stalidzans. SpaceScanner: COPASI wrapper for automated management of global stochastic optimization experiments
2968 -- 0Bonnie Berger, Terry Gaasterland, Thomas Lengauer, Christine A. Orengo, Bruno Gaëta, Scott Markel, Alfonso Valencia. ISCB's initial reaction to New England Journal of Medicine editorial on data sharing
2969 -- 0Alastair M. Kilpatrick. Message from the ISCB: The 5th ISCB Wikipedia competition: coming to a classroom near you?

Volume 33, Issue 17

2611 -- 2614Hebing Chen, Shuai Jiang, Zhuo Zhang, Hao Li, Yiming Lu, Xiaochen Bo. Exploring spatially adjacent TFBS-clustered regions with Hi-C data
2615 -- 2621Jens Lichtenberg, Laura Elnitski, David M. Bodine. SigSeeker: a peak-calling ensemble approach for constructing epigenetic signatures
2622 -- 2630Keqin Liu, Dominik Beck, Julie A. I. Thoms, Liang Liu, Weiling Zhao, John E. Pimanda, Xiaobo Zhou. Annotating function to differentially expressed LincRNAs in myelodysplastic syndrome using a network-based method
2631 -- 2641Xinjie Hui, Yueming Hu, Ming-an Sun, Xingsheng Shu, Rongfei Han, Qinggang Ge, Yejun Wang. EBT: a statistic test identifying moderate size of significant features with balanced power and precision for genome-wide rate comparisons
2642 -- 2650Nicolò Navarin, Fabrizio Costa. An efficient graph kernel method for non-coding RNA functional prediction
2651 -- 2657Weiwei Zhang, Hao Feng, Hao Wu, Xiaoqi Zheng. Accounting for tumor purity improves cancer subtype classification from DNA methylation data
2658 -- 2665Yeeleng Scott Vang, Xiaohui Xie. HLA class I binding prediction via convolutional neural networks
2666 -- 2674Tsukasa Fukunaga, Michiaki Hamada. RIblast: an ultrafast RNA-RNA interaction prediction system based on a seed-and-extension approach
2675 -- 2683Dapeng Xiong, Jianyang Zeng, Haipeng Gong. A deep learning framework for improving long-range residue-residue contact prediction using a hierarchical strategy
2684 -- 2690Daniel W. A. Buchan, David T. Jones. EigenTHREADER: analogous protein fold recognition by efficient contact map threading
2691 -- 2698Hongfu Liu, Rui Zhao, Hongsheng Fang, Feixiong Cheng, Yun Fu, Yang-Yu Liu. Entropy-based consensus clustering for patient stratification
2699 -- 2705Mingli Lei, Jia Xu, Li-Ching Huang, Lily Wang, Jing Li. Network module-based model in the differential expression analysis for RNA-seq
2706 -- 2714Qianqian Shi, Chuanchao Zhang, Minrui Peng, Xiangtian Yu, Tao Zeng, Juan Liu, Luonan Chen. Pattern fusion analysis by adaptive alignment of multiple heterogeneous omics data
2715 -- 2722Jian Ma, Cameron P. Casey, Xueyun Zheng, Yehia M. Ibrahim, Christopher S. Wilkins, Ryan S. Renslow, Dennis G. Thomas, Samuel H. Payne, Matthew E. Monroe, Richard D. Smith, Justin G. Teeguarden, Erin S. Baker, Thomas O. Metz. PIXiE: an algorithm for automated ion mobility arrival time extraction and collision cross section calculation using global data association
2723 -- 2730Mona Alshahrani, Mohammed Asif Khan, Omar Maddouri, Akira R. Kinjo, Núria Queralt-Rosinach, Robert Hoehndorf. Neuro-symbolic representation learning on biological knowledge graphs
2731 -- 2736Michael J. Bell, Phillip W. Lord. On patterns and re-use in bioinformatics databases
2737 -- 2739Kieran O'Neill, Mark Hills, Mike Gottlieb, Matthew Borkowski, Aly Karsan, Peter M. Lansdorp. Assembling draft genomes using contiBAIT
2740 -- 2742Giles Miclotte, Stéphane Plaisance, Stephane Rombauts, Yves Van de Peer, Pieter Audenaert, Jan Fostier. OMSim: a simulator for optical map data
2743 -- 2745Anthony Chiu, Mahmood Ayub, Caroline Dive, Ged Brady, Crispin J. Miller. twoddpcr: an R/Bioconductor package and Shiny app for Droplet Digital PCR analysis
2746 -- 2749Alice Héliou, Solon P. Pissis, Simon J. Puglisi. emMAW: computing minimal absent words in external memory
2750 -- 2752Bo Liu, Tao Jiang, S. M. Yiu, Junyi Li, Yadong Wang. rMFilter: acceleration of long read-based structure variation calling by chimeric read filtering
2753 -- 2755Alex T. Müller, Gisela Gabernet, Jan A. Hiss, Gisbert Schneider. modlAMP: Python for antimicrobial peptides
2756 -- 2758Jiawei Wang, Bingjiao Yang, Jerico Nico De Leon Revote, André Leier, Tatiana T. Marquez-Lago, Geoffrey I. Webb, Jiangning Song, Kuo-Chen Chou, Trevor Lithgow. POSSUM: a bioinformatics toolkit for generating numerical sequence feature descriptors based on PSSM profiles
2759 -- 2761Marek Kokot, Maciej Dlugosz, Sebastian Deorowicz. KMC 3: counting and manipulating k-mer statistics
2762 -- 2764Roberto R. Expósito, Jorge Veiga, Jorge González-Domínguez, Juan Touriño. MarDRe: efficient MapReduce-based removal of duplicate DNA reads in the cloud
2765 -- 2767Robert Kleffner, Jeff Flatten, Andrew Leaver-Fay, David Baker, Justin B. Siegel, Firas Khatib, Seth Cooper. Foldit Standalone: a video game-derived protein structure manipulation interface using Rosetta
2768 -- 2771David K. Brown, David L. Penkler, Olivier Sheik Amamuddy, Caroline Ross, Ali Rana Atilgan, Canan Atilgan, Özlem Tastan Bishop. MD-TASK: a software suite for analyzing molecular dynamics trajectories
2772 -- 2773Andrew Anand Brown. veqtl-mapper: variance association mapping for molecular phenotypes
2774 -- 2775Francesco Del Carratore, Andris Jankevics, Rob Eisinga, Tom Heskes, Fangxin Hong, Rainer Breitling. RankProd 2.0: a refactored bioconductor package for detecting differentially expressed features in molecular profiling datasets
2776 -- 2778Gad Abraham, Yixuan Qiu, Michael Inouye. FlashPCA2: principal component analysis of Biobank-scale genotype datasets
2779 -- 2780Sergi Hervas, Esteve Sanz, Sònia Casillas, John E. Pool, Antonio Barbadilla. PopFly: the Drosophila population genomics browser
2781 -- 2783Katherine Maia McCoy, Margaret L. Antonio, Tim van Opijnen. MAGenTA: a Galaxy implemented tool for complete Tn-Seq analysis and data visualization
2784 -- 2786Judong Shen, Kijoung Song, Andrew J. Slater, Enrico Ferrero, Matthew R. Nelson. STOPGAP: a database for systematic target opportunity assessment by genetic association predictions
2787 -- 2788Sherlyn Jemimah, K. Yugandhar, M. Michael Gromiha. PROXiMATE: a database of mutant protein-protein complex thermodynamics and kinetics
2789 -- 0Erdi Kucuk, Justin Chu, Benjamin P. Vandervalk, S. Austin Hammond, René L. Warren, Inanç Birol. Kollector: transcript-informed, targeted de novo assembly of gene loci
2790 -- 0M. Altenbuchinger, P. Schwarzfischer, T. Rehberg, J. Reinders, Ch. W. Kohler, W. Gronwald, J. Richter, M. Szczepanowski, N. Masqué-Soler, W. Klapper, Peter J. Oefner, R. Spang. Molecular signatures that can be transferred across different omics platforms

Volume 33, Issue 16

2431 -- 2435Donald W. Lee, Gary R. Whittaker. Use of AAScatterPlot tool for monitoring the evolution of the hemagglutinin cleavage site in H9 avian influenza viruses
2436 -- 2445Xiao-fei Zhang, Le Ou-Yang, Hong Yan. Incorporating prior information into differential network analysis using non-paranormal graphical models
2446 -- 2454Claudia Paicu, Irina Mohorianu, Matthew B. Stocks, Ping Xu, Aurore Coince, Martina Billmeier, Tamas Dalmay, Vincent Moulton, Simon Moxon. miRCat2: accurate prediction of plant and animal microRNAs from next-generation sequencing datasets
2455 -- 2463Sivan Leviyang, Igor Griva, Sergio Ita, Welkin E. Johnson. A penalized regression approach to haplotype reconstruction of viral populations arising in early HIV/SIV infection
2464 -- 2470M. Salvatore, Per Warholm, Nanjiang Shu, W. Basile, Arne Elofsson. SubCons: a new ensemble method for improved human subcellular localization predictions
2471 -- 2478Alejandro Ochoa, Mona Singh. Domain prediction with probabilistic directional context
2479 -- 2486Mélanie Boudard, Dominique Barth, Julie Bernauer, Alain Denise, Johanne Cohen. GARN2: coarse-grained prediction of 3D structure of large RNA molecules by regret minimization
2487 -- 2495Anand Sastry, Jonathan Monk, Hanna Tegel, Mathias Uhlen, Bernhard O. Palsson, Johan Rockberg, Elizabeth Brunk. Machine learning in computational biology to accelerate high-throughput protein expression
2496 -- 2503Balachandran Manavalan, Jooyoung Lee. SVMQA: support-vector-machine-based protein single-model quality assessment
2504 -- 2512Sabrina Rashid, Darrell N. Kotton, Ziv Bar-Joseph. TASIC: determining branching models from time series single cell data
2513 -- 2522Keelin Greenlaw, Elena Szefer, Jinko Graham, Mary Lesperance, Farouk S. Nathoo. A Bayesian group sparse multi-task regression model for imaging genetics
2523 -- 2531Majed Alzahrani, Hiroyuki Kuwahara, Wei Wang, Xin Gao. Gracob: a novel graph-based constant-column biclustering method for mining growth phenotype data
2532 -- 2538Xiaoyuan Zhou, Guofeng Meng, Christine Nardini, Hongkang Mei. Systemic evaluation of cellular reprogramming processes exploiting a novel R-tool: eegc
2539 -- 2546Uri Shaham, Kelly P. Stanton, Jun Zhao, Huamin Li, Khadir Raddassi, Ruth R. Montgomery, Yuval Kluger. Removal of batch effects using distribution-matching residual networks
2547 -- 2554Matthias Hörtenhuber, Enrique M. Toledo, Erik Smedler, Ernest Arenas, Seth Malmersjö, Lauri Louhivuori, Per Uhlén. Mapping genes for calcium signaling and their associated human genetic disorders
2555 -- 2562Tao Zeng, Bian Wu, Shuiwang Ji. DeepEM3D: approaching human-level performance on 3D anisotropic EM image segmentation
2563 -- 2569Corinna Blasse, Stephan Saalfeld, Raphaël Etournay, Andreas Sagner, Suzanne Eaton, Eugene W. Myers. PreMosa: extracting 2D surfaces from 3D microscopy mosaics
2570 -- 2572Alice C. L. Parodi, Laura M. Sangalli, Simone Vantini, Bruno Amati, Piercesare Secchi, Marco J. Morelli. FunChIP: an R/Bioconductor package for functional classification of ChIP-seq shapes
2573 -- 2574Patrick Czeczko, Steven C. Greenway, A. P. Jason de Koning. EzMap: a simple pipeline for reproducible analysis of the human virome
2575 -- 2576Renato A. C. dos Santos, Gustavo H. Goldman, Diego Mauricio Riaño-Pachón. ploidyNGS: visually exploring ploidy with Next Generation Sequencing data
2577 -- 2579Shengfeng Huang, Mingjing Kang, Anlong Xu. HaploMerger2: rebuilding both haploid sub-assemblies from high-heterozygosity diploid genome assembly
2580 -- 2582Felipe da Veiga Leprevost, Björn A. Grüning, Saulo Aflitos, Hannes L. Röst, Julian Uszkoreit, Harald Barsnes, Marc Vaudel, Pablo Moreno, Laurent Gatto, Jonas Weber, Mingze Bai, Rafael C. Jimenez, Timo Sachsenberg, Julianus Pfeuffer, Roberto Vera Alvarez, Johannes Griss, Alexey I. Nesvizhskii, Yasset Pérez-Riverol. BioContainers: an open-source and community-driven framework for software standardization
2583 -- 2585Sebastian Beier, Thomas Thiel, Thomas Münch, Uwe Scholz, Martin Mascher. MISA-web: a web server for microsatellite prediction
2586 -- 2588Jinyu Yang, Xin Chen, Adam McDermaid, Qin Ma. DMINDA 2.0: integrated and systematic views of regulatory DNA motif identification and analyses
2589 -- 2590Hitesh Patel, Tobias Brinkjost, Oliver Koch. PyGOLD: a python based API for docking based virtual screening workflow generation
2591 -- 2593José Fernández Navarro, Joel Sjöstrand, Fredrik Salmén, Joakim Lundeberg, Patrik L. Ståhl. ST Pipeline: an automated pipeline for spatial mapping of unique transcripts
2594 -- 2595Paul Saary, Kristoffer Forslund, Peer Bork, Falk Hildebrand. RTK: efficient rarefaction analysis of large datasets
2596 -- 2597James J. Kelley, Shay Maor, Min Kyung Kim, Anatoliy Lane, Desmond S. Lun. MOST-visualization: software for producing automated textbook-style maps of genome-scale metabolic networks
2598 -- 2600Martin Larralde, Thomas N. Lawson, Ralf J. M. Weber, Pablo Moreno, Kenneth Haug, Philippe Rocca-Serra, Mark R. Viant, Christoph Steinbeck, Reza M. Salek. mzML2ISA & nmrML2ISA: generating enriched ISA-Tab metadata files from metabolomics XML data
2601 -- 2603Daniel Cannon, Jeremy J. Yang, Stephen L. Mathias, Oleg Ursu, Subramani Mani, Anna Waller, Stephan C. Schürer, Lars Juhl Jensen, Larry A. Sklar, Cristian Bologa, Tudor I. Oprea. TIN-X: target importance and novelty explorer
2604 -- 2606David Weichselbaum, Bojan Zagrovic, Anton A. Polyansky. Fuento: functional enrichment for bioinformatics
2607 -- 2608Carlos Horro, Martin Cook, Teresa K. Attwood, Michelle D. Brazas, John M. Hancock, Patricia M. Palagi, Manuel Corpas, Rafael C. Jimenez. BioCIDER: a Contextualisation InDEx for biological Resources discovery
2609 -- 0Elizabeth Baskin, Rick Farouni, Ewy A. Mathé. ALTRE: workflow for defining ALTered regulatory elements using chromatin accessibility data
2610 -- 0Xiang Cheng, Shu-Guang Zhao, Xuan Xiao, Kuo-Chen Chou. iATC-mISF: a multi-label classifier for predicting the classes of anatomical therapeutic chemicals

Volume 33, Issue 15

2251 -- 2257Xiuwen Zheng, Stephanie M. Gogarten, Michael F. Lawrence, Adrienne Stilp, Matthew P. Conomos, Bruce S. Weir, Cathy C. Laurie, David Levine. SeqArray - a storage-efficient high-performance data format for WGS variant calls
2258 -- 2265Georg Stricker, Alexander Engelhardt, Daniel Schulz, Matthias Schmid, Achim Tresch, Julien Gagneur. GenoGAM: genome-wide generalized additive models for ChIP-Seq analysis
2266 -- 2272Maximilian Knoll, Jürgen Debus, Amir Abdollahi. cnAnalysis450k: an R package for comparative analysis of 450k/EPIC Illumina methylation array derived copy number data
2273 -- 2280Zhicong Huang, Huang Lin, Jacques Fellay, Zoltan Kutalik, Jean-Pierre Hubaux. SQC: secure quality control for meta-analysis of genome-wide association studies
2281 -- 2287Hsin-Nan Lin, Wen-Lian Hsu. Kart: a divide-and-conquer algorithm for NGS read alignment
2288 -- 2295Shuxiang Ruan, S. Joshua Swamidass, Gary D. Stormo. BEESEM: estimation of binding energy models using HT-SELEX data
2296 -- 2306Baoji He, S. M. Mortuza, Yanting Wang, Hong-bin Shen, Yang Zhang. NeBcon: protein contact map prediction using neural network training coupled with naïve Bayes classifiers
2307 -- 2313Robert Brown, Gleb Kichaev, Nicholas Mancuso, James Boocock, Bogdan Pasaniuc. Enhanced methods to detect haplotypic effects on gene expression
2314 -- 2321Hirotaka Matsumoto, Hisanori Kiryu, Chikara Furusawa, Minoru S. H. Ko, Shigeru B. H. Ko, Norio Gouda, Tetsutaro Hayashi, Itoshi Nikaido. SCODE: an efficient regulatory network inference algorithm from single-cell RNA-Seq during differentiation
2322 -- 2329Steven H. Wu, Rachel Schwartz, David J. Winter, Donald F. Conrad, Reed A. Cartwright. Estimating error models for whole genome sequencing using mixtures of Dirichlet-multinomial distributions
2330 -- 2336Maggie Haitian Wang, Haoyi Weng, Rui Sun, Jack Lee, William Ka Kei Wu, Ka Chun Chong, Benny Zee. A Zoom-Focus algorithm (ZFA) to locate the optimal testing region for rare variant association tests
2337 -- 2344Nansu Zong, Hyeoneui Kim, Victoria Ngo, Olivier Harismendy. Deep mining heterogeneous networks of biomedical linked data to predict novel drug-target associations
2345 -- 2353Hyun-Seob Song, Noam Goldberg, Ashutosh Mahajan, Doraiswami Ramkrishna. Sequential computation of elementary modes and minimal cut sets in genome-scale metabolic networks using alternate integer linear programming
2354 -- 2362Cheng-Hong Yang, Li-Yeh Chuang, Yu-Da Lin. CMDR based differential evolution identifies the epistatic interaction in genome-wide association studies
2363 -- 2371Yinxia Lou, Yue Zhang, Tao Qian, Fei Li, Shufeng Xiong, Donghong Ji. A transition-based joint model for disease named entity recognition and normalization
2372 -- 2378Weijia Zhang, Thuc Duy Le, Lin Liu 0003, Zhi-Hua Zhou, Jiuyong Li. Mining heterogeneous causal effects for personalized cancer treatment
2379 -- 2380Yosuke Nishimura, Takashi Yoshida, Megumi Kuronishi, Hideya Uehara, Hiroyuki Ogata, Susumu Goto. ViPTree: the viral proteomic tree server
2381 -- 2383Raymond G. Cavalcante, Maureen A. Sartor. annotatr: genomic regions in context
2384 -- 2385Feifei Xiao, Yue Niu, Ning Hao, Yanxun Xu, Zhilin Jin, Heping Zhang. modSaRa: a computationally efficient R package for CNV identification
2386 -- 2388Andrew J. Gartland, Nicholas Kullman, Allan C. deCamp, Graham Clenaghan, Wayne Yang, Craig A. Magaret, Paul Thatcher Edlefsen, Peter B. Gilbert. SieveSifter: a web-based tool for visualizing the sieve analyses of HIV-1 vaccine efficacy trials
2389 -- 2391Pedro J. Torres, Robert A. Edwards, Katelyn McNair. PARTIE: a partition engine to separate metagenomic and amplicon projects in the Sequence Read Archive
2392 -- 2394Timothy G. Vaughan. IcyTree: rapid browser-based visualization for phylogenetic trees and networks
2395 -- 2396Inanc Soylu, Stefano M. Marino. Cpipe: a comprehensive computational platform for sequence and structure-based analyses of Cysteine residues
2397 -- 2398Noé Fernández-Pozo, Yi Zheng, Stephen I. Snyder, Philippe Nicolas, Yoshihito Shinozaki, Zhangjun Fei, Carmen Catala, James J. Giovannoni, Jocelyn K. C. Rose, Lukas A. Mueller. The Tomato Expression Atlas
2399 -- 2401Jing Wang, David C. Samuels, Yu Shyr, Yan Guo. StrandScript: evaluation of Illumina genotyping array design and strand correction
2402 -- 2404Alessandro Romanel, Tuo Zhang, Olivier Elemento, Francesca Demichelis. EthSEQ: ethnicity annotation from whole exome sequencing data
2405 -- 2407Matti Pirinen, Christian Benner, Pekka Marttinen, Marjo-Riitta Järvelin, Manuel A. Rivas, Samuli Ripatti. biMM: efficient estimation of genetic variances and covariances for cohorts with high-dimensional phenotype measurements
2408 -- 2409Zhiqiang Hu, Chen Sun, Kuang-chen Lu, Xixia Chu, Yue Zhao, Jinyuan Lu, Jianxin Shi, Chaochun Wei. EUPAN enables pan-genome studies of a large number of eukaryotic genomes
2410 -- 2412Åsmund Flobak, Miguel Vazquez, Astrid Lægreid, Alfonso Valencia. CImbinator: a web-based tool for drug synergy analysis in small- and large-scale datasets
2413 -- 2415Aleksandr Ianevski, Liye He, Tero Aittokallio, Jing Tang. SynergyFinder: a web application for analyzing drug combination dose-response matrix data
2416 -- 2418Michael B. Mundy, Helena Mendes-Soares, Nicholas Chia. Mackinac: a bridge between ModelSEED and COBRApy to generate and analyze genome-scale metabolic models
2419 -- 2420Thomas Naake, Emmanuel Gaquerel. MetCirc: navigating mass spectral similarity in high-resolution MS/MS metabolomics data
2421 -- 2423Nikolas Pontikos, Jing Yu, Ismail Moghul, Lucy Withington, Fiona Blanco-Kelly, Tom Vulliamy, Tsz Lun Ernest Wong, Cian Murphy, Valentina Cipriani, Alessia Fiorentino, Gavin Arno, Daniel Greene, Julius O. B. Jacobsen, Tristan Clark, David S. Gregory, Andrea M. Nemeth, Stephanie Halford, Chris F. Inglehearn, Susan Downes, Graeme C. Black, Andrew R. Webster, Alison J. Hardcastle, Ukirdc, Vincent Plagnol. Phenopolis: an open platform for harmonization and analysis of genetic and phenotypic data
2424 -- 2426Ignacio Arganda-Carreras, Verena Kaynig, Curtis Rueden, Kevin W. Eliceiri, Johannes E. Schindelin, Albert Cardona, H. Sebastian Seung. Trainable Weka Segmentation: a machine learning tool for microscopy pixel classification
2427 -- 2428Pere Ràfols, Sonia Torres, Noelia Ramírez, Esteban del Castillo, Oscar Yanes, Jesús Brezmes, Xavier Correig. rMSI: an R package for MS imaging data handling and visualization
2429 -- 2430Kieran O'Neill, Vivek Rai, Alastair M. Kilpatrick. The International Society for Computational Biology and WikiProject Computational Biology: celebrating 10 years of collaboration towards open access

Volume 33, Issue 14

0 -- 0Pang Wei Koh, Emma Pierson, Anshul Kundaje. Denoising genome-wide histone ChIP-seq with convolutional neural networks
0 -- 0Kymberleigh A. Pagel, Vikas Pejaver, Guan Ning Lin, Hyun-Jun Nam, Matthew E. Mort, David N. Cooper, Jonathan Sebat, Lilia M. Iakoucheva, Sean D. Mooney, Predrag Radivojac. When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variants
0 -- 0Muhammad Ammad-ud-din, Suleiman A. Khan, Krister Wennerberg, Tero Aittokallio. Systematic identification of feature combinations for predicting drug response with Bayesian multi-view multi-task linear regression
0 -- 0Mark A. Hallen, Bruce Randall Donald. CATS (Coordinates of Atoms by Taylor Series): protein design with backbone flexibility in all locally feasible directions
0 -- 0Mirco Michel, David Menéndez Hurtado, Karolis Uziela, Arne Elofsson. Large-scale structure prediction by improved contact predictions and model quality assessment
0 -- 0. ISMB/ECCB 2017 PROCEEDINGS PAPERS COMMITTEE
0 -- 0Lila Rieber, Shaun Mahony. miniMDS: 3D structural inference from high-resolution Hi-C data
0 -- 0Xiaoke Hao, Chanxiu Li, Jingwen Yan, Xiaohui Yao, Shannon L. Risacher, Andrew J. Saykin, Li Shen 0001, Daoqiang Zhang. Identification of associations between genotypes and longitudinal phenotypes via temporally-constrained group sparse canonical correlation analysis
0 -- 0Lin Zhu 0008, Hong-Bo Zhang, De-Shuang Huang. Direct AUC optimization of regulatory motifs
0 -- 0Mohsen Zakeri, Avi Srivastava, Fatemeh Almodaresi, Robert Patro. Improved data-driven likelihood factorizations for transcript abundance estimation
0 -- 0Lei Ding, Daniel J. McDonald. Predicting phenotypes from microarrays using amplified, initially marginal, eigenvector regression
0 -- 0Omer Weissbrod, Elior Rahmani, Regev Schweiger, Saharon Rosset, Eran Halperin. Association testing of bisulfite-sequencing methylation data via a Laplace approximation
0 -- 0Anupama Jha, Matthew R. Gazzara, Yoseph Barash. Integrative deep models for alternative splicing
0 -- 0Michael Estrin, Haim J. Wolfson. SnapDock - template-based docking by Geometric Hashing
0 -- 0Juraj Michalik, Hélène Touzet, Yann Ponty. Efficient approximations of RNA kinetics landscape using non-redundant sampling
0 -- 0. Author Index
0 -- 0Min Xu, Xiaoqi Chai, Hariank Muthakana, Xiaodan Liang, Ge Yang, Tzviya Zeev-Ben-Mordehai, Eric P. Xing. Deep learning-based subdivision approach for large scale macromolecules structure recovery from electron cryo tomograms
0 -- 0Francesca Petralia, Vasily N. Aushev, Kalpana Gopalakrishnan, Maya Kappil, Nyan W. Khin, Jia Chen, Susan L. Teitelbaum, Pei Wang. A new method to study the change of miRNA-mRNA interactions due to environmental exposures
0 -- 0Prashant Pandey, Michael A. Bender, Rob Johnson, Robert Patro. deBGR: an efficient and near-exact representation of the weighted de Bruijn graph
0 -- 0Martina Fischer, Benjamin Strauch, Bernhard Y. Renard. Abundance estimation and differential testing on strain level in metagenomics data
0 -- 0Atefeh Kazeroonian, Fabian J. Theis, Jan Hasenauer. A scalable moment-closure approximation for large-scale biochemical reaction networks
0 -- 0Niko Beerenwinkel, Yana Bromberg. ISMB/ECCB 2017 proceedings
0 -- 0Guillaume Marçais, David Pellow, Daniel Bork, Yaron Orenstein, Ron Shamir, Carl Kingsford. Improving the performance of minimizers and winnowing schemes
0 -- 0Jing Guo, Jie Zheng. HopLand: single-cell pseudotime recovery using continuous Hopfield network-based modeling of Waddington's epigenetic landscape
0 -- 0Yoichiro Nakatani, Aoife McLysaght. Genomes as documents of evolutionary history: a probabilistic macrosynteny model for the reconstruction of ancestral genomes
0 -- 0Ishita K. Khan, Mansurul Bhuiyan, Daisuke Kihara. DextMP: deep dive into text for predicting moonlighting proteins
0 -- 0Gizem Sogancioglu, Hakime Öztürk, Arzucan Özgür. BIOSSES: a semantic sentence similarity estimation system for the biomedical domain
0 -- 0Xiongtao Ruan, Christoph Wülfing, Robert F. Murphy. Image-based spatiotemporal causality inference for protein signaling networks
0 -- 0Clément-Marie Train, Natasha Glover, Gaston H. Gonnet, Adrian M. Altenhoff, Christophe Dessimoz. Orthologous Matrix (OMA) algorithm 2.0: more robust to asymmetric evolutionary rates and more scalable hierarchical orthologous group inference
0 -- 0Stefan Avey, Subhasis Mohanty, Jean Wilson, Heidi Zapata, Samit R. Joshi, Barbara Siconolfi, Sui Tsang, Albert C. Shaw, Steven H. Kleinstein. Multiple network-constrained regressions expand insights into influenza vaccination responses
0 -- 0Maryam Habibi, Leon Weber, Mariana L. Neves, David Luis Wiegandt, Ulf Leser. Deep learning with word embeddings improves biomedical named entity recognition
0 -- 0Pinar Kavak, Yen-Yi Lin, Ibrahim Numanagic, Hossein Asghari, Tunga Güngör, Can Alkan, Faraz Hach. Discovery and genotyping of novel sequence insertions in many sequenced individuals
0 -- 0Eugenio Cinquemani, Valérie Laroute, Muriel Cocaign-Bousquet, Hidde de Jong, Delphine Ropers. Estimation of time-varying growth, uptake and excretion rates from dynamic metabolomics data
0 -- 0C.-H. Lee, Eleazar Eskin, Buhm Han. Increasing the power of meta-analysis of genome-wide association studies to detect heterogeneous effects
0 -- 0Dennis Pischel, Kai Sundmacher, Robert J. Flassig. Efficient simulation of intrinsic, extrinsic and external noise in biochemical systems
0 -- 0Chiara Damiani, Marzia Di Filippo, Dario Pescini, Davide Maspero, Riccardo Colombo, Giancarlo Mauri. popFBA: tackling intratumour heterogeneity with Flux Balance Analysis
0 -- 0Djork-Arné Clevert, Thomas Unterthiner, Gundula Povysil, Sepp Hochreiter. Rectified factor networks for biclustering of omics data
0 -- 0Sai Zhang, Hailin Hu, Tao Jiang, Lei Zhang, Jianyang Zeng. TITER: predicting translation initiation sites by deep learning
0 -- 0Gryte Satas, Benjamin J. Raphael. Tumor phylogeny inference using tree-constrained importance sampling
0 -- 0Xu Min, Wanwen Zeng, Ning Chen, Ting Chen, Rui Jiang. Chromatin accessibility prediction via convolutional long short-term memory networks with k-mer embedding
0 -- 0Sean Robinson, Jaakko Nevalainen, Guillaume Pinna, Anna Campalans, J. Pablo Radicella, Laurent Guyon. Incorporating interaction networks into the determination of functionally related hit genes in genomic experiments with Markov random fields
0 -- 0Dat Duong, Lisa Gai, Sagi Snir, Eun Yong Kang, Buhm Han, Jae Hoon Sul, Eleazar Eskin. Applying meta-analysis to genotype-tissue expression data from multiple tissues to identify eQTLs and increase the number of eGenes
0 -- 0Yohei Rosen, Jordan Eizenga, Benedict Paten. Modelling haplotypes with respect to reference cohort variation graphs
0 -- 0Mingfu Shao, Jianzhu Ma, Sheng Wang 0001. DeepBound: accurate identification of transcript boundaries via deep convolutional neural fields
0 -- 0Yang Yang, Ruochi Zhang, Shashank Singh 0005, Jian Ma. Exploiting sequence-based features for predicting enhancer-promoter interactions
0 -- 0Marinka Zitnik, Jure Leskovec. Predicting multicellular function through multi-layer tissue networks
0 -- 0M. Altenbuchinger, P. Schwarzfischer, T. Rehberg, J. Reinders, Ch. W. Kohler, W. Gronwald, J. Richter, M. Szczepanowski, N. Masqué-Soler, W. Klapper, Peter J. Oefner, R. Spang. Molecular signatures that can be transferred across different omics platforms
0 -- 0Vipin Vijayan, Dominic Critchlow, Tijana Milenkovic. Alignment of dynamic networks
2071 -- 2077Erik L. Clarke, Sesh A. Sundararaman, Stephanie N. Seifert, Frederic D. Bushman, Beatrice H. Hahn, Dustin Brisson. swga: a primer design toolkit for selective whole genome amplification
2078 -- 2081Shudong Wang, Sicheng He, Fayou Yuan, Xinjie Zhu. Tagging SNP-set selection with maximum information based on linkage disequilibrium structure in genome-wide association studies
2082 -- 2088Lorian Schaeffer, Harold Pimentel, Nicolas Bray, Páll Melsted, Lior Pachter. Pseudoalignment for metagenomic read assignment
2089 -- 2096Milad Miladi, Alexander Junge, Fabrizio Costa, Stefan E. Seemann, Jakob Hull Havgaard, Jan Gorodkin, Rolf Backofen. RNAscClust: clustering RNA sequences using structure conservation and graph based motifs
2097 -- 2105Zhen Gao, Jianhua Ruan. Computational modeling of in vivo and in vitro protein-DNA interactions by multiple instance learning
2106 -- 2113Luciano Censoni, Heloisa dos Santos Muniz, Leandro Martínez. A network model predicts the intensity of residue-protein thermal coupling
2114 -- 2122Amélie Héliou, Dominik Budday, Rasmus Fonseca, Henry van den Bedem. Fast, clash-free RNA conformational morphing using molecular junctions
2123 -- 2130Xiaoyu Song, Gen Li, Zhenwei Zhou, Xianling Wang, Iuliana Ionita-Laza, Ying Wei. QRank: a novel quantile regression tool for eQTL discovery
2131 -- 2139Musheng Li, Xueying Xie, Jing Zhou, Mengying Sheng, Xiaofeng Yin, Eun-A Ko, Tong Zhou, Wanjun Gu. Quantifying circular RNA expression from RNA-seq data using model-based framework
2140 -- 2147Lin Wang, Silvia Liu, Ying Ding, Shin-sheng Yuan, Yen-Yi Ho, George C. Tseng. Meta-analytic framework for liquid association
2148 -- 2155Jade Yu Cheng, Thomas Mailund, Rasmus Nielsen. Fast admixture analysis and population tree estimation for SNP and NGS data
2156 -- 2164Nil Mamano, Wayne B. Hayes. SANA: simulated annealing far outperforms many other search algorithms for biological network alignment
2165 -- 2172Mojdeh Faraji, Eberhard O. Voit. Stepwise inference of likely dynamic flux distributions from metabolic time series data
2173 -- 2181Zengmiao Wang, Huaying Fang, Nelson L. S. Tang, Minghua Deng. VCNet: vector-based gene co-expression network construction and its application to RNA-seq data
2182 -- 2190Murad Megjhani, Pedro Correa de Sampaio, Julienne Leigh Carstens, Raghu Kalluri, Badrinath Roysam. Morphologically constrained spectral unmixing by dictionary learning for multiplex fluorescence microscopy
2191 -- 2193Charles Curnin, Assaf Gordon, Yaniv Erlich. DNA Compass: a secure, client-side site for navigating personal genetic information
2194 -- 2196Matthias Monfort, Eileen E. M. Furlong, Charles Girardot. Dynamix: dynamic visualization by automatic selection of informative tracks from hundreds of genomic datasets
2197 -- 2198Asher Haug-Baltzell, Sean A. Stephens, Sean Davey, Carlos Eduardo Scheidegger, Eric Lyons. SynMap2 and SynMap3D: web-based whole-genome synteny browsers
2199 -- 2201Koon-Kiu Yan, Galip Gürkan Yardimci, Chengfei Yan, William S. Noble, Mark Gerstein. HiC-spector: a matrix library for spectral and reproducibility analysis of Hi-C contact maps
2202 -- 2204Gregory W. Vurture, Fritz J. Sedlazeck, Maria Nattestad, Charles J. Underwood, Han Fang, James Gurtowski, Michael C. Schatz. GenomeScope: fast reference-free genome profiling from short reads
2205 -- 2206Konstantin S. Yarygin, Boris Kovarsky, Tanya Bibikova, Damir Melnikov, Alexander V. Tyakht, Dmitry G. Alexeev. ResistoMap - online visualization of human gut microbiota antibiotic resistome
2207 -- 2208Robert D. Stewart, Mick Watson. poRe GUIs for parallel and real-time processing of MinION sequence data
2209 -- 2211Felix Simkovic, Jens M. H. Thomas, Daniel J. Rigden. ConKit: a python interface to contact predictions
2212 -- 2213Sandrine Perrin, Cyril Firmo, Sophie Lemoine, Stéphane Le Crom, Laurent Jourdren. Aozan: an automated post-sequencing data-processing pipeline
2214 -- 2215Qi Wu, Zu-Guo Yu, Jianyi Yang. DLTree: efficient and accurate phylogeny reconstruction using the dynamical language method
2216 -- 2217Jinkai Wang, Yang Pan, Shihao Shen, Lan Lin, Yi Xing. rMATS-DVR: rMATS discovery of differential variants in RNA
2218 -- 2220Robert Petryszak, Nuno A. Fonseca, Anja Füllgrabe, Laura Huerta, Maria Keays, Y. Amy Tang, Alvis Brazma. The RNASeq-er API - a gateway to systematically updated analysis of public RNA-seq data
2221 -- 2223Thomas O. McDonald, Franziska Michor. SIApopr: a computational method to simulate evolutionary branching trees for analysis of tumor clonal evolution
2224 -- 2225Christopher Heffelfinger, Christopher A. Fragoso, Mathias Lorieux. Constructing linkage maps in the genomics era with MapDisto 2.0
2226 -- 2228Gautier Stoll, Barthélémy Caron, Eric Viara, Aurélien Dugourd, Andrei Zinovyev, Aurélien Naldi, Guido Kroemer, Emmanuel Barillot, Laurence Calzone. MaBoSS 2.0: an environment for stochastic Boolean modeling
2229 -- 2231Sascha Herzinger, Wei Gu, Venkata P. Satagopam, Serge Eifes, Kavita Rege, Adriano Barbosa-Silva, Reinhard Schneider 0002, On behalf of the eTRIKS Consortium. SmartR: an open-source platform for interactive visual analytics for translational research data
2232 -- 2234Daniel Schlauch, Joseph N. Paulson, Albert Young, Kimberly Glass, John Quackenbush. Estimating gene regulatory networks with pandaR
2235 -- 2237Zhiwei Zhou, Xin Xiong, Zheng-Jiang Zhu. MetCCS predictor: a web server for predicting collision cross-section values of metabolites in ion mobility-mass spectrometry based metabolomics
2238 -- 2240Istemi Bahceci, Ugur Dogrusoz, Konnor C. La, Özgün Babur, Jianjiong Gao, Nikolaus Schultz. PathwayMapper: a collaborative visual web editor for cancer pathways and genomic data
2241 -- 2242Clemens Messerschmidt, Manuel Holtgrewe, Dieter Beule. HLA-MA: simple yet powerful matching of samples using HLA typing results
2243 -- 2244Christiana N. Fogg, Diane E. Kovats, Bonnie Berger. Message from the ISCB: 2017 ISCB Innovator Award Given to Aviv Regev
2245 -- 2246Christiana N. Fogg, Diane E. Kovats, Bonnie Berger. Message from the ISCB: 2017 ISCB Accomplishment by a Senior Scientist Award Given to Pavel Pevzner
2247 -- 2248Christiana N. Fogg, Diane E. Kovats, Bonnie Berger. Message from the ISCB: 2017 ISCB Overton Prize Awarded to Christoph Bock
2249 -- 2250Christiana N. Fogg, Diane E. Kovats, Bonnie Berger. Message from the ISCB: 2017 Outstanding Contributions to ISCB Award Given to Fran Lewitter

Volume 33, Issue 13

1911 -- 1915Morena Pappalardo, Ian G. Reddin, Diego Cantoni, Jeremy S. Rossman, Martin Michaelis, Mark N. Wass. Changes associated with Ebola virus adaptation to novel species
1916 -- 1920Pengyi Yang, Andrew Oldfield, Taiyun Kim, Andrian Yang, Jean Yee Hwa Yang, Joshua W. K. Ho. Integrative analysis identifies co-dependent gene expression regulation of BRG1 and CHD7 at distal regulatory sites in embryonic stem cells
1921 -- 1929Musa Nur Gabere, William Stafford Noble. Empirical comparison of web-based antimicrobial peptide prediction tools
1930 -- 1936Bite Yang, Feng Liu, Chao Ren, Zhangyi Ouyang, Ziwei Xie, Xiaochen Bo, Wenjie Shu. BiRen: predicting enhancers with a deep-learning-based model using the DNA sequence alone
1937 -- 1943Yugo Shimizu, Hiroyuki Ogata, Susumu Goto. Discriminating the reaction types of plant type III polyketide synthases
1944 -- 1952Yun Zhang, David J. Topham, Juilee Thakar, Xing Qiu. FUNNEL-GSEA: FUNctioNal ELastic-net regression in time-course gene set enrichment analysis
1953 -- 1962Sascha Jung, András Hartmann, Antonio del Sol. RefBool: a reference-based algorithm for discretizing gene expression data
1963 -- 1971Changshuai Wei, Qing Lu. A generalized association test based on U statistics
1972 -- 1979Daniel Schlauch, Heide Loehlein Fier, Christoph Lange 0003. Identification of genetic outliers due to sub-structure and cryptic relationships
1980 -- 1986Sucheendra K. Palaniappan, François Bertaux, Matthieu Pichené, Eric Fabre, Grégory Batt, Blaise Genest. Abstracting the dynamics of biological pathways using information theory: a case study of apoptosis pathway
1987 -- 1994Sahar Ansari, Michele Donato, Nafiseh Saberian, Sorin Draghici. An approach to infer putative disease-specific mechanisms using neighboring gene networks
1995 -- 2001Yu Chen, Yonghong Wang, Jens Nielsen. Systematic inference of functional phosphorylation events in yeast metabolism
2002 -- 2009Vlad Popovici, Eva Budinska, Ladislav Dusek, Michal Kozubek, Fred Bosman. Image-based surrogate biomarkers for molecular subtypes of colorectal cancer
2010 -- 2019William J. Godinez, Imtiaz Hossain, Stanley E. Lazic, John W. Davies, Xian Zhang. A multi-scale convolutional neural network for phenotyping high-content cellular images
2020 -- 2028Oliver Hilsenbeck, Michael Schwarzfischer, Dirk Loeffler, Sotiris Dimopoulos, Simon Hastreiter, Carsten Marr, Fabian J. Theis, Timm Schroeder. fastER: a user-friendly tool for ultrafast and robust cell segmentation in large-scale microscopy
2029 -- 2031Yu Liu, Sha Sun, Timothy Bredy, Marcelo Wood, Robert C. Spitale, Pierre Baldi. MotifMap-RNA: a genome-wide map of RBP binding sites
2032 -- 2033Jacob E. Munro, Sally L. Dunwoodie, Eleni Giannoulatou. SVPV: a structural variant prediction viewer for paired-end sequencing datasets
2034 -- 2036Rogan Magee, Phillipe Loher, Eric Londin, Isidore Rigoutsos. Threshold-seq: a tool for determining the threshold in short RNA-seq datasets
2037 -- 2039Petr Danecek, Shane A. McCarthy. BCFtools/csq: haplotype-aware variant consequences
2040 -- 2041Xavier Watkins, Leyla J. Garcia, Sangya Pundir, Maria Jesus Martin, The UniProt Consortium. ProtVista: visualization of protein sequence annotations
2042 -- 2044Dominik Kopczynski, Harald Barsnes, Pål R. Njølstad, Albert Sickmann, Marc Vaudel, Robert Ahrends. PeptideMapper: efficient and versatile amino acid sequence and tag mapping
2045 -- 2046Tomasz Magdziarz, Karolina Mitusinska, Sandra Goldowska, Alicja Pluciennik, Michal Stolarczyk, Magdalena Lugowska, Artur Góra. AQUA-DUCT: a ligands tracking tool
2047 -- 2049Jianjiong Gao, Andreas Prlic, Chunxiao Bi, Wolfgang Bluhm, Dimitris Dimitropoulos, Dong Xu, Philip E. Bourne, Peter W. Rose. BioJava-ModFinder: identification of protein modifications in 3D structures from the Protein Data Bank
2050 -- 2052Shian Su, Charity W. Law, Casey Ah-Cann, Marie-Liesse Asselin-Labat, Marnie E. Blewitt, Matthew E. Ritchie. Glimma: interactive graphics for gene expression analysis
2053 -- 2055Michal Sharabi-Schwager, Etti Or, Ron Ophir. ctsGE - clustering subgroups of expression data
2056 -- 2058Daniel Taliun, Sonia P. Chothani, Sebastian Schönherr, Lukas Forer, Michael Boehnke, Gonçalo R. Abecasis, Chaolong Wang. LASER server: ancestry tracing with genotypes or sequence reads
2059 -- 2062Zachary A. Szpiech, Alexandra Blant, Trevor J. Pemberton. GARLIC: Genomic Autozygosity Regions Likelihood-based Inference and Classification
2063 -- 2064Felipe Albrecht, Markus List, Christoph Bock, Thomas Lengauer. DeepBlueR: large-scale epigenomic analysis in R
2065 -- 2067Qi Liu, Changjun Ding, Yanguang Chu, Weixi Zhang, Ganggang Guo, Jiafei Chen, Xiaohua Su. Pln24NT: a web resource for plant 24-nt siRNA producing loci
2068 -- 2070Jungsul Lee, ChulHee Choi. Oncopression: gene expression compendium for cancer with matched normal tissues

Volume 33, Issue 12

1751 -- 1757Hashem A. Shihab, Mark F. Rogers, Colin Campbell, Tom R. Gaunt. HIPred: an integrative approach to predicting haploinsufficient genes
1758 -- 1764Feng-Biao Guo, Chuan Dong, Hong-Li Hua, Shuo Liu, Hao Luo, Hong-Wan Zhang, Yan-Ting Jin, Kai-Yue Zhang. Accurate prediction of human essential genes using only nucleotide composition and association information
1765 -- 1772Hokeun Sun, Ya Wang, Yong Chen, Yun Li, Shuang Wang. pETM: a penalized Exponential Tilt Model for analysis of correlated high-dimensional DNA methylation data
1773 -- 1781Ralph Patrick, Bostjan Kobe, Kim-Anh Lê Cao, Mikael Bodén. PhosphoPICK-SNP: quantifying the effect of amino acid variants on protein phosphorylation
1782 -- 1788Erdi Kucuk, Justin Chu, Benjamin P. Vandervalk, S. Austin Hammond, René L. Warren, Inanç Birol. Kollector: transcript-informed, targeted de novo assembly of gene loci
1789 -- 1797Jingwen Pei, Yufeng Wu. STELLS2: fast and accurate coalescent-based maximum likelihood inference of species trees from gene tree topologies
1798 -- 1805Guy Baele, Philippe Lemey, Andrew Rambaut, Marc A. Suchard. Adaptive MCMC in Bayesian phylogenetics: an application to analyzing partitioned data in BEAST
1806 -- 1813Iain H. Moal, Didier Barradas-Bautista, Brian Jiménez-García, Mieczyslaw Torchala, Arjan van der Velde, Thom Vreven, Zhiping Weng, Paul A. Bates, Juan Fernández-Recio. IRaPPA: information retrieval based integration of biophysical models for protein assembly selection
1814 -- 1819Yina Gu, Da-wei Li, Rafael Brüschweiler. Statistical database analysis of the role of loop dynamics for protein-protein complex formation and allostery
1820 -- 1828Felipe Llinares-López, Laetitia Papaxanthos, Dean A. Bodenham, Damian Roqueiro, COPDGene Investigators, Karsten M. Borgwardt. Genome-wide genetic heterogeneity discovery with categorical covariates
1829 -- 1836Biaobin Jiang, Kyle Kloster, David F. Gleich, Michael Gribskov. AptRank: an adaptive PageRank model for protein function prediction on bi-relational graphs
1837 -- 1844Evi Berchtold, Gergely Csaba, Ralf Zimmer. RelExplain - integrating data and networks to explain biological processes
1845 -- 1851Claudia Hernandez-Armenta, David Ochoa, Emanuel J. V. Gonçalves, Julio Saez-Rodriguez, Pedro Beltrao. Benchmarking substrate-based kinase activity inference using phosphoproteomic data
1852 -- 1858Juan Miguel Cejuela, Aleksandar Bojchevski, Carsten Uhlig, Rustem Bekmukhametov, Sanjeev Kumar Karn, Shpend Mahmuti, Ashish Baghudana, Ankit Dubey, Venkata P. Satagopam, Burkhard Rost. nala: text mining natural language mutation mentions
1859 -- 1866Lu Wang, Daniele Durante, Rex E. Jung, David B. Dunson. Bayesian network-response regression
1867 -- 1869Brent S. Pedersen, Aaron R. Quinlan. cyvcf2: fast, flexible variant analysis with Python
1870 -- 1872Elior Rahmani, Reut Yedidim, Liat Shenhav, Regev Schweiger, Omer Weissbrod, Noah Zaitlen, Eran Halperin. GLINT: a user-friendly toolset for the analysis of high-throughput DNA-methylation array data
1873 -- 1875Wei-Zhi Song, Torsten Thomas. Binning_refiner: improving genome bins through the combination of different binning programs
1876 -- 1878Adam Price, Cynthia Gibas. Simulome: a genome sequence and variant simulator
1879 -- 1880Simone Marini, Nelson Nazzicari, Filippo Biscarini, Guang-Zhong Wang. Dscam1 web server: online prediction of Dscam1 self- and hetero-affinity
1881 -- 1882Yuanqiang Zou, Zhiqiang Wu, Lizong Deng, Aiping Wu, Fan Wu, Kenli Li, Taijiao Jiang, Yousong Peng. cooccurNet: an R package for co-occurrence network construction and analysis
1883 -- 1885André R. F. Silva, Diogo B. Lima, Alejandro Leyva, Rosario Duran, Carlos Batthyany, Priscila F. Aquino, Juliana C. Leal, Jimmy E. Rodriguez, Gilberto B. Domont, Marlon D. M. Santos, Julia Chamot-Rooke, Valmir C. Barbosa, Paulo C. Carvalho. DiagnoProt: a tool for discovery of new molecules by mass spectrometry
1886 -- 1888Joseph W. Brown, Joseph F. Walker, Stephen A. Smith. Phyx: phylogenetic tools for unix
1889 -- 1891Damiano Piovesan, Ian Walsh, Giovanni Minervini, Silvio C. E. Tosatto. FELLS: fast estimator of latent local structure
1892 -- 1894Genevieve L. Stein-O'Brien, Jacob L. Carey, Waishing Lee, Michael Considine, Alexander V. Favorov, Emily Flam, Theresa Guo, Sijia Li, Luigi Marchionni, Thomas Sherman, Shawn Sivy, Daria A. Gaykalova, Ronald McKay, Michael F. Ochs, Carlo Colantuoni, Elana J. Fertig. PatternMarkers & GWCoGAPS for novel data-driven biomarkers via whole transcriptome NMF
1895 -- 1897Alexandre Fort, Nikolaos I. Panousis, Marco Garieri, Stylianos E. Antonarakis, Tuuli Lappalainen, Emmanouil T. Dermitzakis, Olivier Delaneau. MBV: a method to solve sample mislabeling and detect technical bias in large combined genotype and sequencing assay datasets
1898 -- 1899Ramón Díaz-Uriarte. OncoSimulR: genetic simulation with arbitrary epistasis and mutator genes in asexual populations
1900 -- 1901Victor Trevino, José G. Tamez-Peña. VALORATE: fast and accurate log-rank test in balanced and unbalanced comparisons of survival curves and cancer genomics
1902 -- 1904Kevin Titeca, Pieter Meysman, Kris Laukens, Lennart Martens, Jan Tavernier, Sven Eyckerman. sfinx: an R package for the elimination of false positives from affinity purification-mass spectrometry datasets
1905 -- 1906Daniel Cuevas, Robert A. Edwards. PMAnalyzer: a new web interface for bacterial growth curve analysis
1907 -- 1909Ilan Y. Smoly, Eugene Lerman, Michal Ziv-Ukelson, Esti Yeger Lotem. MotifNet: a web-server for network motif analysis

Volume 33, Issue 11

1591 -- 1595Shuai Zhang, Chunxia Qin, Guoqiong Cao, Limin Guo, Chengqiang Feng, Wensheng Zhang. Genome-wide analysis of DNA methylation profiles in a senescence-accelerated mouse prone 8 brain using whole-genome bisulfite sequencing
1596 -- 1603Hernando G. Suarez, Bjoern E. Langer, Pradnya Ladde, Michael Hiller. chainCleaner improves genome alignment specificity and sensitivity
1604 -- 1612Thomas Lin Pedersen. Hierarchical sets: analyzing pangenome structure through scalable set visualizations
1613 -- 1620Goro Terai, Satoshi Kamegai, Akito Taneda, Kiyoshi Asai. Evolutionary design of multiple genes encoding the same protein
1621 -- 1629Amrita Roy Choudhury, Tiejun Cheng, Lon Phan, Stephen H. Bryant, Yanli Wang. Supporting precision medicine by data mining across multi-disciplines: an integrative approach for generating comprehensive linkages between single nucleotide variants (SNVs) and drug-binding sites
1630 -- 1638Paschalia Kapli, S. Lutteropp, Jiajie Zhang, Kassian Kobert, Pavlos Pavlidis, Alexandros Stamatakis, Tomás Flouri. Multi-rate Poisson tree processes for single-locus species delimitation under maximum likelihood and Markov chain Monte Carlo
1639 -- 1646Martin Nettling, Hendrik Treutler, Jesús Cerquides, Ivo Grosse. Unrealistic phylogenetic trees may improve phylogenetic footprinting
1647 -- 1655Chanin Tolson Woods, Alain Laederach. Classification of RNA structure change by 'gazing' at experimental data
1656 -- 1663Castrense Savojardo, Piero Fariselli, Pier Luigi Martelli, Rita Casadio. ISPRED4: interaction sites PREDiction in protein structures with a refining grammar model
1664 -- 1671Wei Tian, Meishan Lin, Hammad Naveed, Jie Liang. Efficient computation of transfer free energies of amino acids in beta-barrel membrane proteins
1672 -- 1680Koji Iwayama, Yuri Aisaka, Natsumaro Kutsuna, Atsushi J. Nagano. FIT: statistical modeling tool for transcriptome dynamics under fluctuating field conditions
1681 -- 1688Cheng-Yu Ma, Yi-Ping Phoebe Chen, Bonnie Berger, Chung-Shou Liao. Identification of protein complexes by integrating multiple alignment of protein interaction networks
1689 -- 1695Hao-Chih Lee, Roman Kosoy, Christine E. Becker, Joel T. Dudley, Brian A. Kidd. Automated cell type discovery and classification through knowledge transfer
1696 -- 1702Jiao Zhang, Sam Kwong, Yuheng Jia, Ka Chun Wong. NSSRF: global network similarity search with subgraph signatures and its applications
1703 -- 1711Ruby Peters, Marta Benthem Muñiz, Juliette Griffié, David J. Williamson, George W. Ashdown, Christian D. Lorenz, Dylan M. Owen. Quantification of fibrous spatial point patterns from single-molecule localization microscopy (SMLM) data
1712 -- 1720Zhiqing Zhang, Nikolay V. Kuzmin, Marie Louise Groot, Jan C. de Munck. Extracting morphologies from third harmonic generation images of structurally normal human brain tissue
1721 -- 1722Christopher M. Schroeder, Franz J. Hilke, Markus W. Löffler, Michael Bitzer, Florian Lenz, Marc Sturm. A comprehensive quality control workflow for paired tumor-normal NGS experiments
1723 -- 1724Ted Wong, Ira W. Deveson, Simon A. Hardwick, Tim R. Mercer. ANAQUIN: a software toolkit for the analysis of spike-in controls for next generation sequencing
1725 -- 1726Lauren M. Brinkac, Erin Beck, Jason M. Inman, Pratap Venepally, Derrick E. Fouts, Granger G. Sutton. LOCUST: a custom sequence locus typer for classifying microbial isolates
1727 -- 1729Arnald Alonso, Brittany N. Lasseigne, Kelly Williams, Josh Nielsen, Ryne C. Ramaker, Andrew A. Hardigan, Bobbi Johnston, Brian S. Roberts, Sara J. Cooper, Sara Marsal, Richard M. Myers. aRNApipe: a balanced, efficient and distributed pipeline for processing RNA-seq data in high-performance computing environments
1730 -- 1732Bruno Fosso, Monica Santamaria, M. D'Antonio, D. Lovero, G. Corrado, E. Vizza, N. Pássaro, A. R. Garbuglia, M. R. Capobianchi, M. Crescenzi, Gabriel Valiente, Graziano Pesole. MetaShot: an accurate workflow for taxon classification of host-associated microbiome from shotgun metagenomic data
1733 -- 1734Charalampos Kyriakopoulos, Pascal Giehr, Verena Wolf. H(O)TA: estimation of DNA methylation and hydroxylation levels and efficiencies from time course data
1735 -- 1737Wenzheng Li, Weili Wang, Philip J. Uren, Luiz O. F. Penalva, Andrew D. Smith. Riborex: fast and flexible identification of differential translation from Ribo-seq data
1738 -- 1740Kalle Leppälä, Svend V. Nielsen, Thomas Mailund. admixturegraph: an R package for admixture graph manipulation and fitting
1741 -- 1743Hulda S. Haraldsdóttir, Ben Cousins, Ines Thiele, Ronan M. T. Fleming, Santosh Vempala. CHRR: coordinate hit-and-run with rounding for uniform sampling of constraint-based models
1744 -- 1746Jennifer E. Kyle, Kevin L. Crowell, Cameron P. Casey, Grant M. Fujimoto, Sangtae Kim, Sydney E. Dautel, Richard D. Smith, Samuel H. Payne, Thomas O. Metz. LIQUID: an-open source software for identifying lipids in LC-MS/MS-based lipidomics data
1747 -- 1749Jan J. Domanski, Oliver Beckstein, Bogdan I. Iorga. Ligandbook: an online repository for small and drug-like molecule force field parameters

Volume 33, Issue 10

1431 -- 1436Haihua Liu, Xiaoxiao Shang, Hao Zhu. LncRNA/DNA binding analysis reveals losses and gains and lineage specificity of genomic imprinting in mammals
1437 -- 1446William H. Majoros, Michael Campbell, Carson Holt, Erin K. DeNardo, Doreen Ware, Andrew S. Allen, Mark Yandell, Timothy E. Reddy. High-throughput interpretation of gene structure changes in human and nonhuman resequencing data, using ACE
1447 -- 1456Feng Zeng, ZiCheng Wang, Ying Wang, Jizhong Zhou, Ting Chen. Large-scale 16S gene assembly using metagenomics shotgun sequences
1457 -- 1463Li-na Wang, Shao-Ping Shi, Hao-Dong Xu, Ping-Ping Wen, Jian-Ding Qiu. Computational prediction of species-specific malonylation sites via enhanced characteristic strategy
1464 -- 1472Tom Paridaens, Glenn Van Wallendael, Wesley De Neve, Peter Lambert. AFRESh: an adaptive framework for compression of reads and assembled sequences with random access functionality
1473 -- 1478Anthony Westbrook, Jordan Ramsdell, Taruna Schuelke, Louisa Normington, R. Daniel Bergeron, W. Kelley Thomas, Matthew D. MacManes. PALADIN: protein alignment for functional profiling whole metagenome shotgun data
1479 -- 1487Qingzhen Hou, Paul F. G. De Geest, Wim F. Vranken, Jaap Heringa, K. Anton Feenstra. Seeing the trees through the forest: sequence-based homo- and heteromeric protein-protein interaction sites prediction using random forest
1488 -- 1496Anjali Soni, Pooja Khurana, Tanya Singh, Bhyravabhotla Jayaram. A DNA intercalation methodology for an efficient prediction of ligand binding pose and energetics
1497 -- 1504Pawel P. Wozniak, Gert Vriend, Malgorzata Kotulska. Correlated mutations select misfolded from properly folded proteins
1505 -- 1513Malathi S. I. Dona, Luke A. Prendergast, Suresh Mathivanan, Shivakumar Keerthikumar, Agus Salim. Powerful differential expression analysis incorporating network topology for next-generation sequencing data
1514 -- 1520Bradley C. Naylor, Michael T. Porter, Elise Wilson, Adam Herring, Spencer Lofthouse, Austin Hannemann, Stephen R. Piccolo, Alan L. Rockwood, John C. Price. DeuteRater: a tool for quantifying peptide isotope precision and kinetic proteomics
1521 -- 1527Niki L. Dimou, Konstantinos D. Tsirigos, Arne Elofsson, Pantelis G. Bagos. GWAR: robust analysis and meta-analysis of genome-wide association studies
1528 -- 1535Xiao-Tai Huang, Yuan Zhu, Leanne Lai Hang Chan, Zhongying Zhao, Hong Yan. Inference of cellular level signaling networks using single-cell gene expression data in Caenorhabditis elegans reveals mechanisms of cell fate specification
1536 -- 1544Yuanlong Liu, Myriam Brossard, Damian Roqueiro, Patricia Margaritte-Jeannin, Chloé Sarnowski, Emmanuelle Bouzigon, Florence Demenais. SigMod: an exact and efficient method to identify a strongly interconnected disease-associated module in a gene network
1545 -- 1553Sumanta Basu, William Duren, Charles R. Evans, Charles F. Burant, George Michailidis, Alla Karnovsky. Sparse network modeling and metscape-based visualization methods for the analysis of large-scale metabolomics data
1554 -- 1560Bharat Panwar, Gilbert S. Omenn, Yuanfang Guan. miRmine: a database of human miRNA expression profiles
1561 -- 1562Mariusz Butkiewicz, Jonathan L. Haines, William S. Bush. Introducing COCOS: codon consequence scanner for annotating reading frame changes induced by stop-lost and frame shift variants
1563 -- 1564Anthony O. Olarerin-George, Samie R. Jaffrey. MetaPlotR: a Perl/R pipeline for plotting metagenes of nucleotide modifications and other transcriptomic sites
1565 -- 1567Maximilian Hastreiter, Tim Jeske, Jonathan Hoser, Michael Kluge, Kaarin Ahomaa, Marie-Sophie Friedl, Sebastian J. Kopetzky, Jan-Dominik Quell, H.-Werner Mewes, Robert Küffner. KNIME4NGS: a comprehensive toolbox for next generation sequencing analysis
1568 -- 1569Dario Beraldi. ASCIIGenome: a command line genome browser for console terminals
1570 -- 1571Xing Tang, Arunima Srivastava, Huayang Liu, Raghu Machiraju, Kun Huang, Gustavo Leone. annoPeak: a web application to annotate and visualize peaks from ChIP-seq/ChIP-exo-seq
1572 -- 1574Putri W. Novianti, Barbara C. Snoek, Saskia M. Wilting, Mark A. van de Wiel. Better diagnostic signatures from RNAseq data through use of auxiliary co-data
1575 -- 1577Umberto Ferraro Petrillo, Gianluca Roscigno, Giuseppe Cattaneo, Raffaele Giancarlo. FASTdoop: a versatile and efficient library for the input of FASTA and FASTQ files for MapReduce Hadoop bioinformatics applications
1578 -- 1580Karolis Uziela, David Menéndez Hurtado, Nanjiang Shu, Björn Wallner, Arne Elofsson. ProQ3D: improved model quality assessments using deep learning
1581 -- 1582Daniel E. Cook, Erik C. Andersen. VCF-kit: assorted utilities for the variant call format
1583 -- 1585Jing Guo, Feng Lin, Xiaomeng Zhang, Vivek Tanavde, Jie Zheng. NetLand: quantitative modeling and visualization of Waddington's epigenetic landscape using probabilistic potential
1586 -- 1588P. Derouault, B. Parfait, R. Moulinas, C.-C. Barrot, F. Sturtz, S. Merillou, A.-S. Lia. 'COV'COP' allows to detect CNVs responsible for inherited diseases among amplicons sequencing data
1589 -- 1590Martin Peters, Johann J. Eicher, David D. van Niekerk, Dagmar Waltemath, Jacky L. Snoep. The JWS online simulation database

Volume 33, Issue 1

1 -- 7Wei Yang, Saurabh Sinha. A novel method for predicting activity of cis-regulatory modules, based on a diverse training set
8 -- 16Rafael Rosales, Rodrigo D. Drummond, Renan Valieris, Emmanuel Dias-Neto, Israel T. da Silva. signeR: an empirical Bayesian approach to mutational signature discovery
17 -- 25Sandra L. Taylor, L. Renee Ruhaak, Robert H. Weiss, Karen Kelly, Kyoungmi Kim. Multivariate two-part statistics for analysis of correlated mass spectrometry data from multiple biological specimens
26 -- 34Can Kockan, Faraz Hach, Iman Sarrafi, Robert H. Bell, Brian McConeghy, Kevin Beja, Anne Haegert, Alexander W. Wyatt, Stanislav Volik, Kim N. Chi, Colin Collins, Süleyman Cenk Sahinalp. SiNVICT: ultra-sensitive detection of single nucleotide variants and indels in circulating tumour DNA
35 -- 41Bin Liu 0014, Shanyi Wang, Ren Long, Kuo-Chen Chou. iRSpot-EL: identify recombination spots with an ensemble learning approach
42 -- 48Akinori Awazu. Prediction of nucleosome positioning by the incorporation of frequencies and distributions of three different nucleotide segment lengths into a general pseudo k-tuple nucleotide composition
49 -- 55Matei David, L. J. Dursi, Delia Yao, Paul C. Boutros, Jared T. Simpson. Nanocall: an open source basecaller for Oxford Nanopore sequencing data
56 -- 63Lazaros Mavridis, Robert W. Janes. PDB2CD: a web-based application for the generation of circular dichroism spectra from protein atomic coordinates
64 -- 71Il-Youp Kwak, Wei Pan. Gene- and pathway-based association tests for multiple traits with GWAS summary statistics
72 -- 78Verena Heinrich, Tom Kamphans, Stefan Mundlos, Peter N. Robinson, Peter M. Krawitz. A likelihood ratio-based method to predict exact pedigrees for complex families from next-generation sequencing data
79 -- 86Jie Zheng, Santiago Rodríguez, Charles Laurin, Denis Baird, Lea Trela-Larsen, Mesut A. Erzurumluoglu, Yi Zheng, Jon White, Claudia Giambartolomei, Delilah Zabaneh, Richard Morris, Meena Kumari, Juan P. Casas, Aroon D. Hingorani, David M. Evans, Tom R. Gaunt, Ian N. M. Day. HAPRAP: a haplotype-based iterative method for statistical fine mapping using GWAS summary statistics
87 -- 94Minsuk Kim, Gwanggyu Sun, Dong-Yup Lee, Byung-Gee Kim. BeReTa: a systematic method for identifying target transcriptional regulators to enhance microbial production of chemicals
95 -- 103Igor Marin de Mas, Eric Fanchon, Balázs Papp, Susana G. Kalko, Josep Roca, Marta Cascante. Molecular mechanisms underlying COPD-muscle dysfunction unveiled through a systems medicine approach
104 -- 111Victor Jaravine, Silke Raffegerst, Dolores J. Schendel, Dmitrij Frishman. Assessment of cancer and virus antigens for cross-reactivity in human tissues
112 -- 118Xiaowei Chen, Yajing Hao, Ya Cui, Zhen Fan, Shunmin He, Jianjun Luo, Runsheng Chen. LncVar: a database of genetic variation associated with long non-coding genes
119 -- 121Anuj Gupta, I. King Jordan, Lavanya Rishishwar. stringMLST: a fast k-mer based tool for multilocus sequence typing
122 -- 124Yongchun Zuo, Yuan Li, Yingli Chen, Guangpeng Li, Zhenhe Yan, Lei Yang. PseKRAAC: a flexible web server for generating pseudo K-tuple reduced amino acids composition
125 -- 127M. Stanley Fujimoto, Anton Suvorov, Nicholas O. Jensen, Mark J. Clement, Quinn Snell, Seth M. Bybee. The OGCleaner: filtering false-positive homology clusters
128 -- 129Marta Nascimento, Adriano Sousa, Mário Ramirez, Alexandre P. Francisco, João A. Carriço, Cátia Vaz. PHYLOViZ 2.0: providing scalable data integration and visualization for multiple phylogenetic inference methods
130 -- 132Michael R. McKain, Ryan H. Hartsock, Molly M. Wohl, Elizabeth A. Kellogg. Verdant: automated annotation, alignment and phylogenetic analysis of whole chloroplast genomes
133 -- 134Sébastien Buchoux. FATSLiM: a fast and robust software to analyze MD simulations of membranes
135 -- 136Samuel Wieczorek, Florence Combes, Cosmin Lazar, Quentin Giai Gianetto, Laurent Gatto, Alexia Dorffer, Anne-Marie Hesse, Yohann Couté, Myriam Ferro, Christophe Bruley, Thomas Burger. DAPAR & ProStaR: software to perform statistical analyses in quantitative discovery proteomics
137 -- 138Ilias Georgakopoulos-Soares, Naman Jain, Jesse M. Gray, Martin Hemberg. MPRAnator: a web-based tool for the design of massively parallel reporter assay experiments
139 -- 141Yi Zhong, Theofanis Karaletsos, Philipp Drewe, Vipin T. Sreedharan, David Kuo, Kamini Singh, Hans-Guido Wendel, Gunnar Rätsch. RiboDiff: detecting changes of mRNA translation efficiency from ribosome footprints
142 -- 144Rudy Arthur, Ole Schulz-Trieglaff, Anthony J. Cox, Jared O'Connell. AKT: ancestry and kinship toolkit
145 -- 147Takaya Saito, Marc Rehmsmeier. Precrec: fast and accurate precision-recall and ROC curve calculations in R
148 -- 149Carlo Ravagli, Francois Pognan, Philippe Marc. OntoBrowser: a collaborative tool for curation of ontologies by subject matter experts
150 -- 0Charlotte Siska, Russell Bowler, Katerina Kechris. The discordant method: a novel approach for differential correlation