Journal: Bioinformatics

Volume 32, Issue 9

1281 -- 1285Sebastián Duchêne, Charles S. P. Foster, Simon Y. W. Ho. Estimating the number and assignment of clock models in analyses of multigene datasets
1286 -- 1292Tuan Trieu, Jianlin Cheng. MOGEN: a tool for reconstructing 3D models of genomes from chromosomal conformation capturing data
1293 -- 1300Sean Simmons, Bonnie Berger. Realizing privacy preserving genome-wide association studies
1301 -- 1307Yao-Ting Huang, Chen-Fu Liao. Integration of string and de Bruijn graphs for genome assembly
1308 -- 1315Tanzy M. T. Love, Sung-Yong Park, Elena E. Giorgi, Wendy J. Mack, Alan S. Perelson, Ha Youn Lee. SPMM: estimating infection duration of multivariant HIV-1 infections
1316 -- 1322Xiaowei Wang. Improving microRNA target prediction by modeling with unambiguously identified microRNA-target pairs from CLIP-ligation studies
1323 -- 1330Maria Hauser, Martin Steinegger, Johannes Söding. MMseqs software suite for fast and deep clustering and searching of large protein sequence sets
1331 -- 1337Diego Darriba, Michael Weiß, Alexandros Stamatakis. Prediction of missing sequences and branch lengths in phylogenomic data
1338 -- 1345Amir Nikooienejad, Wenyi Wang, Valen E. Johnson. Bayesian variable selection for binary outcomes in high-dimensional genomic studies using non-local priors
1346 -- 1352Antti Häkkinen, Andre S. Ribeiro. Characterizing rate limiting steps in transcription from RNA production times in live cells
1353 -- 1365Michal P. Switnicki, Malene Juul, Tobias Madsen, Karina D. Sørensen, Jakob S. Pedersen. PINCAGE: probabilistic integration of cancer genomics data for perturbed gene identification and sample classification
1366 -- 1372Dmitry Prokopenko, Julian Hecker, Edwin K. Silverman, Marcello Pagano, Markus M. Nöthen, Christian Dina, Christoph Lange 0003, Heide Loehlein Fier. Utilizing the Jaccard index to reveal population stratification in sequencing data: a simulation study and an application to the 1000 Genomes Project
1373 -- 1379Jonathan H. Young, Michael Peyton, Hyun Seok Kim, Elizabeth McMillan, John D. Minna, Michael A. White, Edward M. Marcotte. Computational discovery of pathway-level genetic vulnerabilities in non-small-cell lung cancer
1380 -- 1387Ahmad Pesaranghader, Stan Matwin, Marina Sokolova, Robert G. Beiko. simDEF: definition-based semantic similarity measure of gene ontology terms for functional similarity analysis of genes
1388 -- 1394Paul Blomstedt, Ritabrata Dutta, Sohan Seth, Alvis Brazma, Samuel Kaski. Modelling-based experiment retrieval: a case study with gene expression clustering
1395 -- 1401Raphaël Marée, Loic Rollus, Benjamin Stevens, Renaud Hoyoux, Gilles Louppe, Remy Vandaele, Jean-Michel Begon, Philipp Kainz, Pierre Geurts, Louis Wehenkel. Collaborative analysis of multi-gigapixel imaging data using Cytomine
1402 -- 1404Frederic Commo, Justin Guinney, Charles Ferté, Brian Bot, Celine Lefebvre, Jean-Charles Soria, Fabrice André. rCGH: a comprehensive array-based genomic profile platform for precision medicine
1405 -- 1407Clovis Galiez, Christophe N. Magnan, François Coste, Pierre Baldi. VIRALpro: a tool to identify viral capsid and tail sequences
1408 -- 1410Ning Leng, Jeea Choi, Li-Fang Chu, James A. Thomson, Christina Kendziorski, Ron M. Stewart. OEFinder: a user interface to identify and visualize ordering effects in single-cell RNA-seq data
1411 -- 1413Karolis Uziela, Björn Wallner. ProQ2: estimation of model accuracy implemented in Rosetta
1414 -- 1416Josef Laimer, Julia Hiebl-Flach, Daniel Lengauer, Peter Lackner. MAESTROweb: a web server for structure-based protein stability prediction
1417 -- 1419Tikira Temu, Matthias Mann 0002, Markus Räschle, Jürgen Cox. Homology-driven assembly of NOn-redundant protEin sequence sets (NOmESS) for mass spectrometry
1420 -- 1422Seung Hwan Lee, Julius H. J. Van der Werf. MTG2: an efficient algorithm for multivariate linear mixed model analysis based on genomic information
1423 -- 1426Xiaowei Zhan, Youna Hu, Bingshan Li, Gonçalo R. Abecasis, Dajiang J. Liu. RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data
1427 -- 1429Oliver Philipp, Heinz D. Osiewacz, Ina Koch. Path2PPI: an R package to predict protein-protein interaction networks for a set of proteins
1430 -- 1432Angie S. Hinrichs, Brian J. Raney, Matthew L. Speir, Brooke L. Rhead, Jonathan Casper, Donna Karolchik, Robert M. Kuhn, Kate R. Rosenbloom, Ann S. Zweig, David Haussler, W. James Kent. UCSC Data Integrator and Variant Annotation Integrator
1433 -- 1435Jian Yang, Gaofeng Deng, Haoyang Cai. ChromothripsisDB: a curated database of chromothripsis
1436 -- 1438Catherine Mooney, Brett A. Becker, Rana Raoof, David C. Henshall. EpimiRBase: a comprehensive database of microRNA-epilepsy associations
1439 -- 1440Andrea Vargas, Marc Angeli, Chiara Pastrello, Rosanne McQuaid, Han Li, Andrea Jurisicova, Igor Jurisica. Robust quantitative scratch assay

Volume 32, Issue 8

1121 -- 1129Yoli Shavit, Barnabas James Walker, Pietro Liò. Hierarchical block matrices as efficient representations of chromosome topologies and their application for 3C data integration
1130 -- 1137Yongzhuang Liu, Jian Liu, Jianguo Lu, Jiajie Peng, Liran Juan, Xiaolin Zhu, Bingshan Li, Yadong Wang. Joint detection of copy number variations in parent-offspring trios
1138 -- 1143Thomas Wolf, Vladimir Shelest, Neetika Nath, Ekaterina Shelest. CASSIS and SMIPS: promoter-based prediction of secondary metabolite gene clusters in eukaryotic genomes
1144 -- 1150Fatma-Elzahraa Eid, Mahmoud ElHefnawi, Lenwood S. Heath. DeNovo: virus-host sequence-based protein-protein interaction prediction
1151 -- 1157Hwee Kim, Yo-Sub Han. OMPPM: online multiple palindrome pattern matching
1158 -- 1162Christoph Peters, Konstantinos D. Tsirigos, Nanjiang Shu, Arne Elofsson. Improved topology prediction using the terminal hydrophobic helices rule
1163 -- 1169Edoardo Milanetti, Domenico Raimondo, Anna Tramontano. Prediction of the permeability of neutral drugs inferred from their solvation properties
1170 -- 1177Jiao Yuan, Peng Zhang, Ya Cui, Jiajia Wang, Geir Skogerbø, Da Wei Huang, Runsheng Chen, Shunmin He. Computational identification of piRNA targets on mouse mRNAs
1178 -- 1184Il-Youp Kwak, Wei Pan. Adaptive gene- and pathway-trait association testing with GWAS summary statistics
1185 -- 1194Jiajie Peng, Tao Wang, Jixuan Wang, Yadong Wang, Jin Chen. Extending gene ontology with gene association networks
1195 -- 1203Vladimir Gligorijevic, Noël Malod-Dognin, Natasa Przulj. Fuse: multiple network alignment via data fusion
1204 -- 1210Helge Hass, Clemens Kreutz, Jens Timmer, Daniel Kaschek. Fast integration-based prediction bands for ordinary differential equation models
1211 -- 1213Tsu-Pei Chiu, Federico Comoglio, Tianyin Zhou, Lin Yang, Renato Paro, Remo Rohs. DNAshapeR: an R/Bioconductor package for DNA shape prediction and feature encoding
1214 -- 1216Li Chen, Zhaohui S. Qin. traseR: an R package for performing trait-associated SNP enrichment analysis in genomic intervals
1217 -- 1219Charles E. Grant, James Johnson, Timothy L. Bailey, William Stafford Noble. cis-regulatory motif clusters
1220 -- 1222Xiaoyu Chen, Ole Schulz-Trieglaff, Richard Shaw, Bret Barnes, Felix Schlesinger, Morten Källberg, Anthony J. Cox, Semyon Kruglyak, Christopher T. Saunders. Manta: rapid detection of structural variants and indels for germline and cancer sequencing applications
1223 -- 1225Sandeep K. Kushwaha, Pallavi Chauhan, Katarina Hedlund, Dag G. Ahrén. NBSPred: a support vector machine-based high-throughput pipeline for plant resistance protein NBSLRR prediction
1226 -- 1228Youri Hoogstrate, René Böttcher, Saskia D. Hiltemann, Peter J. van der Spek, Guido Jenster, Andrew Stubbs. FuMa: reporting overlap in RNA-seq detected fusion genes
1229 -- 1231R. Gonzalo Parra, Cristian Oscar Rohr, Daniel Koile, Carolina Perez-Castro, Patricio Yankilevich. cis-regulatory modules prediction
1232 -- 1234R. T. Good, T. Varghese, John Golz, D. A. Russell, A. Papanicolaou, O. Edwards, C. Robin. OfftargetFinder: a web tool for species-specific RNAi design
1235 -- 1237Leandro E. Lombardi, Marcelo A. Marti, Luciana Capece. CG2AA: backmapping protein coarse-grained structures
1238 -- 1240Daniel Sundfeld, Jakob Hull Havgaard, Alba Cristina Magalhaes Alves de Melo, Jan Gorodkin. Foldalign 2.5: multithreaded implementation for pairwise structural RNA alignment
1241 -- 1243Philipp Angerer, Laleh Haghverdi, Maren Büttner, Fabian J. Theis, Carsten Marr, Florian Buettner. destiny: diffusion maps for large-scale single-cell data in R
1244 -- 1246Petr Smirnov, Zhaleh Safikhani, Nehme Hachem, Dong Wang, Adrian She, Catharina Olsen, Mark Freeman, Heather Selby, Deena M. A. Gendoo, Patrick Grossmann, Andrew H. Beck, Hugo J. W. L. Aerts, Mathieu Lupien, Anna Goldenberg, Benjamin Haibe-Kains. PharmacoGx: an R package for analysis of large pharmacogenomic datasets
1247 -- 1249Gilderlanio S. Araújo, Lucas Henrique C. Lima, Silvana Schneider, Thiago P. Leal, Ana Paula Couto da Silva, Pedro O. S. Vaz de Melo, Eduardo Tarazona-Santos, Marília O. Scliar, Maíra R. Rodrigues. Integrating, summarizing and visualizing GWAS-hits and human diversity with DANCE (Disease-ANCEstry networks)
1250 -- 1252Michael Matschiner. Fitchi: haplotype genealogy graphs based on the Fitch algorithm
1253 -- 1255Daniel Bottomly, Shannon K. McWeeney, Beth Wilmot. HitWalker2: visual analytics for precision medicine and beyond
1256 -- 1258Ahmadreza Ghaffarizadeh, Samuel H. Friedman, Paul Macklin. BioFVM: an efficient, parallelized diffusive transport solver for 3-D biological simulations
1259 -- 1261Maximilian Malek, Rashid Ibragimov, Mario Albrecht, Jan Baumbach. CytoGEDEVO - global alignment of biological networks with Cytoscape
1262 -- 1264Augustin Luna, Özgün Babur, Bülent Arman Aksoy, Emek Demir, Chris Sander. PaxtoolsR: pathway analysis in R using Pathway Commons
1265 -- 1266Jan Bert Van Klinken, Ko Willems van Dijk. FluxModeCalculator: an efficient tool for large-scale flux mode computation
1267 -- 1268Alastair P. Droop. qsubsec: a lightweight template system for defining sun grid engine workflows
1269 -- 1271Dennis Goldfarb, Wei Wang, Michael B. Major. MSAcquisitionSimulator: data-dependent acquisition simulator for LC-MS shotgun proteomics
1272 -- 1274Augustin Luna, Vinodh N. Rajapakse, Fabricio G. Sousa, Jianjiong Gao, Nikolaus Schultz, Sudhir Varma, William C. Reinhold, Chris Sander, Yves Pommier. rcellminer: exploring molecular profiles and drug response of the NCI-60 cell lines in R
1275 -- 1277Damion M. Dooley, Aaron J. Petkau, Gary H. Van Domselaar, William W. L. Hsiao. Sequence database versioning for command line and Galaxy bioinformatics servers
1278 -- 1280Zsuzsanna Püspöki, Daniel Sage, John Paul Ward, Michael Unser. SpotCaliper: fast wavelet-based spot detection with accurate size estimation

Volume 32, Issue 7

961 -- 967Birte Kehr, Páll Melsted, Bjarni V. Halldórsson. PopIns: population-scale detection of novel sequence insertions
968 -- 975Simona Constantinescu, Ewa Szczurek, Pejman Mohammadi, Jörg Rahnenführer, Niko Beerenwinkel. TiMEx: a waiting time model for mutually exclusive cancer alterations
976 -- 983Monica Golumbeanu, Pejman Mohammadi, Niko Beerenwinkel. BMix: probabilistic modeling of occurring substitutions in PAR-CLIP data
984 -- 992Daria Iakovishina, Isabelle Janoueix-Lerosey, Emmanuel Barillot, Mireille Régnier, Valentina Boeva. SV-Bay: structural variant detection in cancer genomes using a Bayesian approach with correction for GC-content and read mappability
993 -- 1000Jie Ren, Kai Song, Minghua Deng, Gesine Reinert, Charles H. Cannon, Fengzhu Sun. Inference of Markovian properties of molecular sequences from NGS data and applications to comparative genomics
1001 -- 1008Yuzhen Ye, Haixu Tang. Utilizing de Bruijn graph of metagenome assembly for metatranscriptome analysis
1009 -- 1015Dmitry Antipov, Anton Korobeynikov, Jeffrey S. McLean, Pavel A. Pevzner. hybridSPAdes: an algorithm for hybrid assembly of short and long reads
1016 -- 1022Lee Mendelowitz, David C. Schwartz, Mihai Pop. Maligner: a fast ordered restriction map aligner
1023 -- 1032Kevin Vervier, Pierre Mahé, Maud Tournoud, Jean-Baptiste Veyrieras, Jean-Philippe Vert. Large-scale machine learning for metagenomics sequence classification
1033 -- 1039Laura DiChiacchio, Michael F. Sloma, David H. Mathews. AccessFold: predicting RNA-RNA interactions with consideration for competing self-structure
1040 -- 1047Martina Fischer, Bernhard Y. Renard. iPQF: a new peptide-to-protein summarization method using peptide spectra characteristics to improve protein quantification
1048 -- 1056Anna Paola Carrieri, Filippo Utro, Laxmi Parida. Sampling ARG of multiple populations under complex configurations of subdivision and admixture
1057 -- 1064Zhanchao Li, Meng-Hua Huang, Wen-Qian Zhong, Zhi-Qing Liu, Yun Xie, Zong Dai, Xiaoyong Zou. Identification of drug-target interaction from interactome network with 'guilt-by-association' principle and topology features
1065 -- 1073Wim Verleyen, Sara Ballouz, Jesse Gillis. Positive and negative forms of replicability in gene network analysis
1074 -- 1079Suzanne M. Paley, Markus Krummenacker, Peter D. Karp. Representation and inference of cellular architecture for metabolic reconstruction and modeling
1080 -- 1082Nour-al-dain Marzouka, Jessica Nordlund, Christofer L. Bäcklin, Gudmar Lönnerholm, Ann-Christine Syvänen, Jonas Carlsson Almlöf. CopyNumber450kCancer: baseline correction for accurate copy number calling from the 450k methylation array
1083 -- 1084Thomas Lacroix, Sylvie Thérond, Marc Rugeri, Pierre Nicolas, Annie Gendrault, Valentin Loux, Jean-François Gibrat. Synchronized navigation and comparative analyses across Ensembl complete bacterial genomes with INSYGHT
1085 -- 1087Andrea Franceschini, Jianyi Lin, Christian von Mering, Lars Juhl Jensen. SVD-phy: improved prediction of protein functional associations through singular value decomposition of phylogenetic profiles
1088 -- 1090Alla Mikheenko, Vladislav Saveliev, Alexey A. Gurevich. MetaQUAST: evaluation of metagenome assemblies
1091 -- 1093Denis Seyres, Elodie Darbo, Laurent Perrin, Carl Herrmann, Aitor González. LedPred: an R/bioconductor package to predict regulatory sequences using support vector machines
1094 -- 1096Jun Cheng, Franziska Metge, Christoph Dieterich. Specific identification and quantification of circular RNAs from sequencing data
1097 -- 1099Deena M. A. Gendoo, Natchar Ratanasirigulchai, Markus S. Schröder, Laia Paré, Joel S. Parker, Aleix Prat, Benjamin Haibe-Kains. Genefu: an R/Bioconductor package for computation of gene expression-based signatures in breast cancer
1100 -- 1102Chee Lee, Snehal Patil, Maureen A. Sartor. RNA-Enrich: a cut-off free functional enrichment testing method for RNA-seq with improved detection power
1103 -- 1105Rongfeng Cui, Molly Schumer, Gil G. Rosenthal. Admix'em: a flexible framework for forward-time simulations of hybrid populations with selection and mate choice
1106 -- 1108Gilles Guillot, Hákon Jónsson, Antoine Hinge, Nabil Manchih, Ludovic Orlando. Accurate continuous geographic assignment from low- to high-density SNP data
1109 -- 1111Lars Barquist, Matthew Mayho, Carla A. Cummins, Amy K. Cain, Christine J. Boinett, Andrew J. Page, Gemma C. Langridge, Michael A. Quail, Jacqueline A. Keane, Julian Parkhill. The TraDIS toolkit: sequencing and analysis for dense transposon mutant libraries
1112 -- 1114Christopher Schmied, Peter Steinbach, Tobias Pietzsch, Stephan Preibisch, Pavel Tomancak. An automated workflow for parallel processing of large multiview SPIM recordings
1115 -- 1117Sebastian Deorowicz, Szymon Grabowski, Idoia Ochoa, Mikel Hernaez, Tsachy Weissman. Comment on: 'ERGC: an efficient referential genome compression algorithm'
1118 -- 1119Subrata Saha, Sanguthevar Rajasekaran. Authors' response to 'Comment on: ERGC: An efficient Referential Genome Compression Algorithm'
1120 -- 0Paulo Gaspar, José Luís Oliveira, Jörg Frommlet, Manuel A. S. Santos, Gabriela R. Moura. EuGene: maximizing synthetic gene design for heterologous expression

Volume 32, Issue 6

801 -- 807Mookyung Cheon, Choongrak Kim, Iksoo Chang. Uncovering multiloci-ordering by algebraic property of Laplacian matrix and its Fiedler vector
808 -- 813Kyle S. Smith, Vinod Kumar Yadav, Shanshan Pei, Daniel A. Pollyea, Craig T. Jordan, Subhajyoti De. SomVarIUS: somatic variant identification from unpaired tissue samples
814 -- 820Gearoid Fox, Fabian Sievers, Desmond G. Higgins. de novo protein structure predictions to measure the quality of very large multiple sequence alignments
821 -- 827Enrique Audain, Yassel Ramos, Henning Hermjakob, Darren R. Flower, Yasset Perez-Riverol. Accurate estimation of isoelectric point of protein and peptide based on amino acid sequences
828 -- 834Goro Terai, Satoshi Kamegai, Kiyoshi Asai. CDSfold: an algorithm for designing a protein-coding sequence with the most stable secondary structure
835 -- 842Filippo Utro, Valeria Di Benedetto, Davide F. V. Corona, Raffaele Giancarlo. The intrinsic combinatorial organization and information theoretic content of a sequence are correlated to the DNA encoded nucleosome organization of eukaryotic genomes
843 -- 849Rhys Heffernan, Abdollah Dehzangi, James G. Lyons, Kuldip K. Paliwal, Alok Sharma, Jihua Wang, Abdul Sattar, Yaoqi Zhou, Yuedong Yang. Highly accurate sequence-based prediction of half-sphere exposures of amino acid residues in proteins
850 -- 858Sangjin Kim, Paul Schliekelman. Prioritizing hypothesis tests for high throughput data
859 -- 866Pierre Pudlo, Jean-Michel Marin, Arnaud Estoup, Jean-Marie Cornuet, Mathieu Gautier, Christian P. Robert. Reliable ABC model choice via random forests
867 -- 874Matthew B. Biggs, Jason A. Papin. Metabolic network-guided binning of metagenomic sequence fragments
875 -- 883S. M. Minhaz Ud-Dean, Rudiyanto Gunawan. Optimal design of gene knockout experiments for gene regulatory network inference
884 -- 892Aristidis G. Vrahatis, Konstantina Dimitrakopoulou, Panos Balomenos, Athanasios K. Tsakalidis, Anastasios Bezerianos. CHRONOS: a time-varying method for microRNA-mediated subpathway enrichment analysis
893 -- 900Martin Pirkl, Elisabeth Hand, Dieter Kube, Rainer Spang. Analyzing synergistic and non-synergistic interactions in signalling pathways using Boolean Nested Effect Models
901 -- 907Yusuke Komiyama, Masaki Banno, Kokoro Ueki, Gul Saad, Kentaro Shimizu. Automatic generation of bioinformatics tools for predicting protein-ligand binding sites
908 -- 917Goksel Misirli, Matteo Cavaliere, William Waites, Matthew R. Pocock, Curtis Madsen, Owen Gilfellon, Ricardo Honorato-Zimmer, Paolo Zuliani, Vincent Danos, Anil Wipat. Annotation of rule-based models with formal semantics to enable creation, analysis, reuse and visualization
918 -- 925Samuel Croset, Joachim Rupp, Martin Romacker. Flexible data integration and curation using a graph-based approach
926 -- 928Xuefeng Wang, Mengjie Chen, Xiaoqing Yu, Natapol Pornputtapong, Hao Chen, Nancy R. Zhang, R. Scott Powers, Michael Krauthammer. Global copy number profiling of cancer genomes
929 -- 931Michael Richter, Ramon Rosselló-Mora, Frank Oliver Glöckner, Jörg Peplies. JSpeciesWS: a web server for prokaryotic species circumscription based on pairwise genome comparison
932 -- 936Joanna Lange, Lucjan Stanislaw Wyrwicz, Gert Vriend. KMAD: knowledge-based multiple sequence alignment for intrinsically disordered proteins
937 -- 939Kun Yang, Giovanni Stracquadanio, Jingchuan Luo, Jef D. Boeke, Joel S. Bader. BioPartsBuilder: a synthetic biology tool for combinatorial assembly of biological parts
940 -- 942Nan Li, Richard I. Ainsworth, Meixin Wu, Bo Ding, Wei Wang. MIEC-SVM: automated pipeline for protein peptide/ligand interaction prediction
943 -- 945Wentao Yang, Katja Dierking, Hinrich Schulenburg. Caenorhabditis elegans-specific gene expression enrichment analysis
946 -- 948Yan Wen, Wenyu Wang, Xiong Guo, Feng Zhang. PAPA: a flexible tool for identifying pleiotropic pathways using genome-wide association study summaries
949 -- 951Tokhir Dadaev, Daniel A. Leongamornlert, Edward J. Saunders, Rosalind Eeles, Zsofia Kote-Jarai. LocusExplorer: a user-friendly tool for integrated visualization of human genetic association data and biological annotations
952 -- 954Ying-Wooi Wan, Genevera I. Allen, Zhandong Liu. TCGA2STAT: simple TCGA data access for integrated statistical analysis in R
955 -- 957Filippo Piccinini, Alexa Kiss, Péter Horváth. CellTracker (not only) for dummies
958 -- 960Dominic Waithe, Mathias P. Clausen, Erdinc Sezgin, Christian Eggeling. FoCuS-point: software for STED fluorescence correlation and time-gated single photon counting

Volume 32, Issue 5

641 -- 649Feng Liu, Chao Ren, Hao Li, Pingkun Zhou, Xiaochen Bo, Wenjie Shu. De novo identification of replication-timing domains in the human genome by deep learning
650 -- 656Zheng Xu, Guosheng Zhang, Fulai Jin, Mengjie Chen, Terrence S. Furey, Patrick F. Sullivan, Zhaohui S. Qin, Ming Hu, Yun Li. A hidden Markov random field-based Bayesian method for the detection of long-range chromosomal interactions in Hi-C data
657 -- 663Tomasz Konopka, Sebastian M. B. Nijman. Comparison of genetic variants in matched samples using thesaurus annotation
664 -- 672Wonyul Lee, Jeffrey S. Morris. Identification of differentially methylated loci using wavelet-based functional mixed models
673 -- 681Lorena Pantano, Marc R. Friedländer, Geòrgia Escaramís, Esther Lizano, Joan Pallarès-Albanell, Isidre Ferrer, Xavier Estivill, Eulalia Martí. Specific small-RNA signatures in the amygdala at premotor and motor stages of Parkinson's disease revealed by deep sequencing analysis
682 -- 689Ben Li, Zhaonan Sun, Qing He, Yu Zhu, Zhaohui S. Qin. Bayesian inference with historical data-based informative priors improves detection of differentially expressed genes
690 -- 696Charlotte Siska, Russell Bowler, Katerina Kechris. The discordant method: a novel approach for differential correlation
697 -- 704Valerio Cestarelli, Giulia Fiscon, Giovanni Felici, Paola Bertolazzi, Emanuel Weitschek. CAMUR: Knowledge extraction from RNA-seq cancer data through equivalent classification rules
705 -- 712Qi Shen, Jiyuan Hu, Ning Jiang, Xiaohua Hu, Zewei Luo, Hong Zhang. contamDE: differential expression analysis of RNA-seq data for contaminated tumor samples
713 -- 721Wei Hao, Minsun Song, John D. Storey. Probabilistic models of genetic variation in structured populations applied to global human studies
722 -- 729Eduardo Palma, Lilian Salinas, Julio Aracena. Enumeration and extension of non-equivalent deterministic update schedules in Boolean networks
730 -- 737Matthias P. Gerstl, Steffen Klamt, Christian Jungreuthmayer, Jürgen Zanghellini. Exact quantification of cellular robustness in genome-scale metabolic networks
738 -- 746Marie Denis, Mahlet G. Tadesse. Evaluation of hierarchical models for integrative genomic analyses
747 -- 754A. Mazouchi, J. N. Milstein. Fast Optimized Cluster Algorithm for Localizations (FOCAL): a spatial cluster analysis for super-resolved microscopy
755 -- 763Hao-Chih Lee, Tao Liao, Yongjie Jessica Zhang, Ge Yang. Shape component analysis: structure-preserving dimension reduction on biological shape spaces
764 -- 766Minh Duc Cao, Devika Ganesamoorthy, Matthew A. Cooper, Lachlan J. M. Coin. Realtime analysis and visualization of MinION sequencing data with npReader
767 -- 769Katharina J. Hoff, Simone Lange, Alexandre Lomsadze, Mark Borodovsky, Mario Stanke. BRAKER1: Unsupervised RNA-Seq-Based Genome Annotation with GeneMark-ET and AUGUSTUS
770 -- 772André Kahles, Jonas Behr, Gunnar Rätsch. MMR: a tool for read multi-mapper resolution
773 -- 775Carmen Maria Livi, Petr Klus, Riccardo Delli Ponti, Gian Gaetano Tartaglia. signature: identification of ribonucleoproteins and RNA-binding regions
776 -- 778Sumit Mukherjee, Supratim Sengupta. Riboswitch Scanner: an efficient pHMM-based web-server to detect riboswitches in genomic sequences
779 -- 781Sneha Mitra, Leelavati Narlikar. de novo promoter architectures from genome-wide transcription start sites
782 -- 785Dietmar Rieder, Thomas Amort, Elisabeth Kugler, Alexandra Lusser, Zlatko Trajanoski. meRanTK: methylated RNA analysis ToolKit
786 -- 788Brant C. Faircloth. PHYLUCE is a software package for the analysis of conserved genomic loci
789 -- 791Sebastian Höhna, Michael R. May, Brian R. Moore. TESS: an R package for efficiently simulating phylogenetic trees and performing Bayesian inference of lineage diversification rates
792 -- 794Florian Kaiser, Alexander Eisold, Sebastian Bittrich, Dirk Labudde. Fit3D: a web application for highly accurate screening of spatial residue patterns in protein structure data
795 -- 797Matthias Steinrücken, Ethan M. Jewett, Yun S. Song. SpectralTDF: transition densities of diffusion processes with time-varying selection parameters, mutation rates and effective population sizes
798 -- 800Brandon R. Thomas, Lily A. Chylek, Joshua Colvin, Suman Sirimulla, Andrew H. A. Clayton, William S. Hlavacek, Richard G. Posner. BioNetFit: a fitting tool compatible with BioNetGen, NFsim and distributed computing environments

Volume 32, Issue 4

481 -- 489Guido Capitani, Jose M. Duarte, Kumaran Baskaran, Spencer Bliven, Joseph C. Somody. Understanding the fabric of protein crystals: computational classification of biological interfaces and crystal contacts
490 -- 496Haoyang Zeng, Tatsunori B. Hashimoto, Daniel D. Kang, David K. Gifford. GERV: a statistical method for generative evaluation of regulatory variants for transcription factor binding
497 -- 504Uwe Baier, Timo Beller, Enno Ohlebusch. Graphical pan-genome analysis with compressed suffix trees and the Burrows-Wheeler transform
505 -- 510M. Kroon, Eric-Wubbo Lameijer, N. Lakenberg, Jayne Y. Hehir-Kwa, D. T. Thung, P. Eline Slagboom, Joost N. Kok, Kai Ye. Detecting dispersed duplications in high-throughput sequencing data using a database-free approach
511 -- 517Massimo Andreatta, Morten Nielsen. Gapped sequence alignment using artificial neural networks: application to the MHC class I system
518 -- 522Sarah Bastkowski, Vincent Moulton, Andreas Spillner 0001, Taoyang Wu. The minimum evolution problem is hard: a link between tree inference and graph clustering problems
523 -- 532Alex Lewin, Habib Saadi, James E. Peters, Aida Moreno-Moral, James C. Lee, Kenneth G. C. Smith, Enrico Petretto, Leonardo Bottolo, Sylvia Richardson. MT-HESS: an efficient Bayesian approach for simultaneous association detection in OMICS datasets, with application to eQTL mapping in multiple tissues
533 -- 541Sheida Nabavi, Daniel Schmolze, Mayinuer Maitituoheti, Sadhika Malladi, Andrew H. Beck. EMDomics: a robust and powerful method for the identification of genes differentially expressed between heterogeneous classes
542 -- 548Qiongshi Lu, Xinwei Yao, Yiming Hu, Hongyu Zhao. GenoWAP: GWAS signal prioritization through integrated analysis of genomic functional annotation
549 -- 556Emile R. Chimusa, Mamana Mbiyavanga, Gaston K. Mazandu, Nicola J. Mulder. ancGWAS: a post genome-wide association study method for interaction, pathway and ancestry analysis in homogeneous and admixed populations
557 -- 562Po-Ju Yao, Ren Hua Chung. SeqSIMLA2_exact: simulate multiple disease sites in large pedigrees with given disease status for diseases with low prevalence
563 -- 570Martin Scharm, Olaf Wolkenhauer, Dagmar Waltemath. An algorithm to detect and communicate the differences in computational models describing biological systems
571 -- 578Thorsten Will, Volkhard Helms. PPIXpress: construction of condition-specific protein interaction networks based on transcript expression
579 -- 586Chen Wang, Gang Hu, Kui Wang, Michal Brylinski, Lei Xie, Lukasz A. Kurgan. PDID: database of molecular-level putative protein-drug interactions in the structural human proteome
587 -- 589Nathan C. Sheffield, Christoph Bock. LOLA: enrichment analysis for genomic region sets and regulatory elements in R and Bioconductor
590 -- 592Heng Li. BGT: efficient and flexible genotype query across many samples
593 -- 595Kathleen Oros Klein, Stepan Grinek, Sasha Bernatsky, Luigi Bouchard, Antonio Ciampi, Ines Colmegna, Jean-Philippe Fortin, Long Gao, Marie-France Hivert, Marie Hudson, Michael S. Kobor, Aurélie Labbe, Julia L. MacIsaac, Michael J. Meaney, Alexander M. Morin, Kieran J. O'Donnell, Tomi Pastinen, Marinus H. Van Ijzendoorn, Gregory Voisin, Celia M. T. Greenwood. funtooNorm: an R package for normalization of DNA methylation data when there are multiple cell or tissue types
596 -- 598Jeffrey Staples, Lynette Ekunwe, Ethan M. Lange, James G. Wilson, Deborah A. Nickerson, Jennifer E. Below. PRIMUS: improving pedigree reconstruction using mitochondrial and Y haplotypes
599 -- 601Cyril Denby Wilkes, Olivier Arnaiz, Linda Sperling. Paramecium interspersed DNA elimination studies
602 -- 604Mayya Sedova, Lukasz Jaroszewski, Adam Godzik. Protael: protein data visualization library for the web
605 -- 607Yu-Wei Wu, Blake A. Simmons, Steven W. Singer. MaxBin 2.0: an automated binning algorithm to recover genomes from multiple metagenomic datasets
608 -- 610François Chevenet, Jean-Philippe Doyon, Céline Scornavacca, Edwin Jacox, Emmanuelle Jousselin, Vincent Berry. SylvX: a viewer for phylogenetic tree reconciliations
611 -- 613Hyojung Ryu, GyuTae Lim, Bong Hyun Sung, Jinhyuk Lee. NMRe: a web server for NMR protein structure refinement with high-quality structure validation scores
614 -- 615Lin Wang, Min Zhang, Emil Alexov. a of proteins, RNAs and DNAs
616 -- 618Alexey G. Kikhney, Alejandro Panjkovich, Anna V. Sokolova, Dmitri I. Svergun. DARA: a web server for rapid search of structural neighbours using solution small angle X-ray scattering data
619 -- 620Hirofumi Suzuki, Takeshi Kawabata, Haruki Nakamura. Omokage search: shape similarity search service for biomolecular structures in both the PDB and EMDB
621 -- 623Matthieu Chartier, Etienne Adriansen, Rafael Najmanovich. IsoMIF Finder: online detection of binding site molecular interaction field similarities
624 -- 626Ming-Huei Chen, Qiong Yang. RVFam: an R package for rare variant association analysis with family data
627 -- 628António Múrias dos Santos, Maria Pilar Cabezas, Ana Isabel Tavares, Raquel Xavier, Madalena Branco. tcsBU: a tool to extend TCS network layout and visualization
629 -- 631Bruce E. Shapiro, Eric Mjolsness. Pycellerator: an arrow-based reaction-like modelling language for biological simulations
632 -- 634Jan Winter, Marco Breinig, Florian Heigwer, Dirk Brügemann, Svenja Leible, Oliver Pelz, Tianzuo Zhan, Michael Boutros. caRpools: an R package for exploratory data analysis and documentation of pooled CRISPR/Cas9 screens
635 -- 637Juan J. Diaz-Montana, Owen J. L. Rackham, Norberto Díaz-Díaz, Enrico Petretto. Web-based Gene Pathogenicity Analysis (WGPA): a web platform to interpret gene pathogenicity from personal genome data
638 -- 640Caterina Barillari, Diana S. M. Ottoz, Juan Mariano Fuentes-Serna, Chandrasekhar Ramakrishnan, Bernd Rinn, Fabian Rudolf. openBIS ELN-LIMS: an open-source database for academic laboratories

Volume 32, Issue 3

321 -- 324Ka Chun Wong, Yue Li, Chengbin Peng. Identification of coupling DNA motif pairs on long-range chromatin interactions in human K562 cells
325 -- 329Michael Knudsen, Dan Søndergaard, Claus Tofting-Olesen, Frederik T. Hansen, Ditlev Egeskov Brodersen, Christian N. S. Pedersen. Computational discovery of specificity-conferring sites in non-ribosomal peptide synthetases
330 -- 337Shaolong Cao, Huaizhen Qin, Alexej Gossmann, Hong-Wen Deng, Yu-Ping Wang. Unified tests for fine-scale mapping and identifying sparse high-dimensional sequence associations
338 -- 344Swati Kaushik, Anu G. Nair, Eshita Mutt, Hari Prasanna Subramanian, Ramanathan Sowdhamini. Rapid and enhanced remote homology detection by cascading hidden Markov model searches in sequence space
345 -- 353Juliana S. Bernardes, Fabio Vieira, Gerson Zaverucha, Alessandra Carbone. A multi-objective optimization approach accurately resolves protein domain architectures
354 -- 361Genivaldo Gueiros Z. Silva, Kevin T. Green, Bas E. Dutilh, Robert A. Edwards. SUPER-FOCUS: a tool for agile functional analysis of shotgun metagenomic data
362 -- 369Bin Liu 0014, Longyun Fang, Ren Long, Xun Lan, Kuo-Chen Chou. k-tuple nucleotide composition
370 -- 377Peter Brown, Wayne Pullan, Yuedong Yang, Yaoqi Zhou. Fast and accurate non-sequential protein structure alignment using a new asymmetric linear sum assignment heuristic
378 -- 387Haiyou Deng, Ya Jia, Yang Zhang. 3DRobot: automated generation of diverse and well-packed protein structure decoys
388 -- 397Isik Baris Fidaner, Ayca Cankorur-Cetinkaya, Duygu Dikicioglu, Betül Kirdar, Ali Taylan Cemgil, Stephen G. Oliver. CLUSTERnGO: a user-defined modelling platform for two-stage clustering of time-series data
398 -- 408Mehrshad Khosraviani, Morteza Saheb Zamani, Gholamreza Bidkhori. FogLight: an efficient matrix-based approach to construct metabolic pathways by search space reduction
409 -- 416Tin Nguyen, Rebecca Tagett, Michele Donato, Cristina Mitrea, Sorin Draghici. A novel bi-level meta-analysis approach: applied to biological pathway analysis
417 -- 423Jeremy Hyrkas, Sophie Clayton, Francois Ribalet, Daniel Halperin, E. Virginia Armbrust, Bill Howe. Scalable clustering algorithms for continuous environmental flow cytometry
424 -- 431Marcel Mischnik, Francesca Sacco, Jürgen Cox, Hans-Christoph Schneider, Matthias Schäfer, Manfred Hendlich, Daniel Crowther, Matthias Mann 0002, Thomas Klabunde. IKAP: A heuristic framework for inference of kinase activities from Phosphoproteomics data
432 -- 440Simon Baker, Ilona Silins, Yufan Guo, Imran Ali, Johan Högberg, Ulla Stenius, Anna Korhonen. Automatic semantic classification of scientific literature according to the hallmarks of cancer
441 -- 443Mitchell J. Sullivan, Nathan L. Bachmann, Peter Timms, Adam Polkinghorne. HapFlow: visualizing haplotypes in sequencing data
444 -- 446Johannes Köster. Rust-Bio: a fast and safe bioinformatics library
447 -- 449Ibrahim Tanyalcin, Carla Al Assaf, Alexander Gheldof, Katrien Stouffs, Willy Lissens, Anna C. Jansen. I-PV: a CIRCOS module for interactive protein sequence visualization
450 -- 452Parth Patel, S. Deepthi Ramachandruni, Atul Kakrana, Mayumi Nakano, Blake C. Meyers. Analysis
453 -- 455Ivan Borozan, Vincent Ferretti. CSSSCL: a python package that uses combined sequence similarity scores for accurate taxonomic classification of long and short sequence reads
456 -- 458Jérôme Mariette, Frédéric Escudié, Philippe Bardou, Nabihoudine Ibouniyamine, Céline Noirot, Marie-Stéphane Trotard, Christine Gaspin, Christophe Klopp. Jflow: a workflow management system for web applications
459 -- 461Danny Incarnato, Francesco Neri, Francesca Anselmi, Salvatore Oliviero. RNA structure framework: automated transcriptome-wide reconstruction of RNA secondary structures from high-throughput structure probing data
462 -- 464Chao Wang, Haicang Zhang, Wei-Mou Zheng, Dong Xu, Jianwei Zhu, Bing Wang, Kang Ning, Shiwei Sun, Shuai Cheng Li, Dongbo Bu. FALCON@home: a high-throughput protein structure prediction server based on remote homologue recognition
465 -- 468Christoph Müssel, Florian Schmid, Tamara J. Blätte, Martin Hopfensitz, Ludwig Lausser, Hans A. Kestler. BiTrinA - multiscale binarization and trinarization with quality analysis
469 -- 471Jun Chen, Allan C. Just, Joel Schwartz, Lifang Hou, Nadereh Jafari, Zhifu Sun, Jean-Pierre A. Kocher, Andrea A. Baccarelli, Xihong Lin. CpGFilter: model-based CpG probe filtering with replicates for epigenome-wide association studies
472 -- 473Weizhong Tu, Haoran Zhang, Juan Liu, Qian-Nan Hu. BioSynther: a customized biosynthetic potential explorer
474 -- 476Tim Schäfer, Andreas Scheck, Daniel Bruneß, Patrick May, Ina Koch. The new protein topology graph library web server
477 -- 479Gaston K. Mazandu, Emile R. Chimusa, Mamana Mbiyavanga, Nicola J. Mulder. A-DaGO-Fun: an adaptable Gene Ontology semantic similarity-based functional analysis tool

Volume 32, Issue 24

3695 -- 3701Hua-Jun Wu, Franziska Michor. A computational strategy to adjust for copy number in tumor Hi-C data
3702 -- 3708Rolf Hilker, Kai Bernd Stadermann, Oliver Schwengers, Evgeny Anisiforov, Sebastian Jaenicke, Bernd Weisshaar, Tobias Zimmermann, Alexander Goesmann. ReadXplorer 2 - detailed read mapping analysis and visualization from one single source
3709 -- 3716Rodrigo Cánovas, Alistair Moffat, Andrew Turpin. CSAM: Compressed SAM format
3717 -- 3728Jack P. Hou, Amin Emad, Gregory J. Puleo, Jian Ma, Olgica Milenkovic. A new correlation clustering method for cancer mutation analysis
3729 -- 3734Lisle E. Mose, Sara R. Selitsky, Lisa M. Bixby, David L. Marron, Michael D. Iglesia, Jonathan S. Serody, Charles M. Perou, Benjamin Vincent, Joel S. Parker. Assembly-based inference of B-cell receptor repertoires from short read RNA sequencing data with V'DJer
3735 -- 3744Minzhu Xie, Qiong Wu, Jianxin Wang, Tao Jiang 0001. H-PoP and H-PoPG: heuristic partitioning algorithms for single individual haplotyping of polyploids
3745 -- 3752Weizhong Lin, Dong Xu. Imbalanced multi-label learning for identifying antimicrobial peptides and their functional types
3753 -- 3759Cristina Frías-López, José F. Sánchez-Herrero, Sara Guirao-Rico, Elisa Mora, Miquel A. Arnedo, Alejandro Sánchez-Gracia, Julio Rozas. DOMINO: development of informative molecular markers for phylogenetic and genome-wide population genetic studies in non-model organisms
3760 -- 3767Jinchao Yu, Raphaël Guérois. PPI4DOCK: large scale assessment of the use of homology models in free docking over more than 1000 realistic targets
3768 -- 3773Jianzhao Gao, Yuedong Yang, Yaoqi Zhou. Predicting the errors of predicted local backbone angles and non-local solvent- accessibilities of proteins by deep neural networks
3774 -- 3781Qiwei Li, David B. Dahl, Marina Vannucci, Hyun Joo, Jerry W. Tsai. KScons: a Bayesian approach for protein residue contact prediction using the knob-socket model of protein tertiary structure
3782 -- 3789Yiyi Liu, Hongyu Zhao. Predicting synergistic effects between compounds through their structural similarity and effects on transcriptomes
3790 -- 3797Eoin C. Whelan, Alexander C. Nwala, Christopher Osgood, Stephan Olariu. Selective mutation accumulation: a computational model of the paternal age effect
3798 -- 3806Andy L. Olivares, Miguel Ángel González Ballester, Jérôme Noailly. Virtual exploration of early stage atherosclerosis
3807 -- 3814Pedro Saa, Lars K. Nielsen. Fast-SNP: a fast matrix pre-processing algorithm for efficient loopless flux optimization of metabolic models
3815 -- 3822Sara Hillenmeyer, Lea K. Davis, Eric R. Gamazon, Edwin H. Cook Jr., Nancy J. Cox, Russ B. Altman. STAMS: STRING-assisted module search for genome wide association studies and application to autism
3823 -- 3825Rachid Ounit, Stefano Lonardi. S
3826 -- 3828Jorge González-Domínguez, Yongchao Liu, Juan Touriño, Bertil Schmidt. MSAProbs-MPI: parallel multiple sequence aligner for distributed-memory systems
3829 -- 3832Bayo Lau, Marghoob Mohiyuddin, John C. Mu, Li Tai Fang, Narges Bani Asadi, Carolina Dallett, Hugo Y. K. Lam. in silico sequencing of lengthy and noisy datatypes
3833 -- 3835Andreas Prlic, Tara Kalro, Roshni Bhattacharya, Cole H. Christie, Stephen K. Burley, Peter W. Rose. Integrating genomic information with protein sequence and 3D atomic level structure at the RCSB protein data bank
3836 -- 3838Solaiappan Manimaran, Heather Selby, Kwame Okrah, Claire Ruberman, Jeffrey T. Leek, John Quackenbush, Benjamin Haibe-Kains, Héctor Corrada Bravo, W. Evan Johnson. BatchQC: interactive software for evaluating sample and batch effects in genomic data
3839 -- 3841Andrew D. Kern, Daniel R. Schrider. Discoal: flexible coalescent simulations with selection
3842 -- 3843Amit Frishberg, Avital Brodt, Yael Steuerman, Irit Gat-Viks. ImmQuant: a user-friendly tool for inferring immune cell-type composition from gene-expression data
3844 -- 3846Aristidis G. Vrahatis, Panos Balomenos, Athanasios K. Tsakalidis, Anastasios Bezerianos. DEsubs: an R package for flexible identification of differentially expressed subpathways using RNA-seq experiments
3847 -- 3849Jamie Soul, Sara L. Dunn, Tim E. Hardingham, Ray P. Boot-Handford, Jean-Marc Schwartz. PhenomeScape: a cytoscape app to identify differentially regulated sub-networks using known disease associations
3850 -- 3851Joseph Ward, Christian Cole, Melanie Febrer, Geoffrey J. Barton. AlmostSignificant: simplifying quality control of high-throughput sequencing data
3852 -- 3854Eisuke Hayakawa, Yoshinori Fujimura, Daisuke Miura. MSIdV: a versatile tool to visualize biological indices from mass spectrometry imaging data
3855 -- 0Arnon Mazza, Konrad Klockmeier, Erich E. Wanker, Roded Sharan. An integer programming framework for inferring disease complexes from network data

Volume 32, Issue 23

3535 -- 3542Niels W. Hanson, Kishori M. Konwar, Steven J. Hallam. LCA*: an entropy-based measure for taxonomic assignment within assembled metagenomes
3543 -- 3551Tianshun Gao, Bing He, Sheng Liu, Heng Zhu, Kai Tan, Jiang Qian. EnhancerAtlas: a resource for enhancer annotation and analysis in 105 human cell/tissue types
3552 -- 3558Alexander V. Alekseyenko. t-test on distances
3559 -- 3565Ruoyan Chen, Yu-Lung Lau, Yan Zhang, Wanling Yang. SRinversion: a tool for detecting short inversions by splitting and re-aligning poorly mapped and unmapped sequencing reads
3566 -- 3574Nicole E. Wheeler, Lars Barquist, Robert A. Kingsley, Paul P. Gardner. A profile-based method for identifying functional divergence of orthologous genes in bacterial genomes
3575 -- 3583Krishna Choudhary, Nathan P. Shih, Fei Deng, Mirko Ledda, Bo Li, Sharon Aviran. Metrics for rapid quality control in RNA structure probing experiments
3584 -- 3592Jing Lu, Heather A. Carlson. ChemTreeMap: an interactive map of biochemical similarity in molecular datasets
3593 -- 3602Ei-Wen Yang, Tao Jiang 0001. SDEAP: a splice graph based differential transcript expression analysis tool for population data
3603 -- 3610Xiang Zhan, Santhosh Girirajan, Ni Zhao, Michael C. Wu, Debashis Ghosh. A novel copy number variants kernel association test with application to autism spectrum disorders studies
3611 -- 3618S. Cogill, L. Wang. Support vector machine model of developmental brain gene expression data for prioritization of Autism risk gene candidates
3619 -- 3626Dong Xu, Meizhuo Zhang, Yanping Xie, Fan Wang, Ming Chen, Kenny Q. Zhu, Jia Wei. DTMiner: identification of potential disease targets through biomedical literature mining
3627 -- 3634Gianluca Corrado, Toma Tebaldi, Fabrizio Costa, Paolo Frasconi, Andrea Passerini. RNAcommender: genome-wide recommendation of RNA-protein interactions
3635 -- 3644Serguei V. S. Pakhomov, Greg Finley, Reed McEwan, Yan Wang, Genevieve B. Melton. Corpus domain effects on distributional semantic modeling of medical terms
3645 -- 3653Vedrana Vidulin, Tomislav Smuc, Fran Supek. Extensive complementarity between gene function prediction methods
3654 -- 3660Shicai Wang, Mihaela A. Mares, Yike Guo. CGDM: collaborative genomic data model for molecular profiling data using NoSQL
3661 -- 3663Louis-Philippe Lemieux Perreault, Marc-André Legault, Géraldine Asselin, Marie-Pierre Dube. genipe: an automated genome-wide imputation pipeline with automatic reporting and statistical tools
3664 -- 3666Rickard Hammarén, Chandan Pal, Johan Bengtsson-Palme. FARAO: the flexible all-round annotation organizer
3667 -- 3669Zongli Xu, Jack A. Taylor, Yuet-Kin Leung, Shuk-Mei Ho, Liang Niu. oxBS-MLE: an efficient method to estimate 5-methylcytosine and 5-hydroxymethylcytosine in paired bisulfite and oxidative bisulfite treated DNA
3670 -- 3672Jamie Waese, Asher Pasha, Tingting Wang, Anna van Weringh, David S. Guttman, Nicholas J. Provart. Gene Slider: sequence logo interactive data-visualization for education and research
3673 -- 3675Erwin Holzhauser, Ping Ge, Shaojie Zhang. WebSTAR3D: a web server for RNA 3D structural alignment
3676 -- 3678Li C. Xue, João P. G. L. M. Rodrigues, Panagiotis L. Kastritis, Alexandre M. J. J. Bonvin, Anna Vangone. PRODIGY: a web server for predicting the binding affinity of protein-protein complexes
3679 -- 3681Jasmine Dumas, Michael A. Gargano, Garrett M. Dancik. shinyGEO: a web-based application for analyzing gene expression omnibus datasets
3682 -- 3684Thomas Eder, Florian Grebien, Thomas Rattei. NVT: a fast and simple tool for the assessment of RNA-seq normalization strategies
3685 -- 3687Zhou Lan, Yize Zhao, Jian Kang, Tianwei Yu. Bayesian network feature finder (BANFF): an R package for gene network feature selection
3688 -- 3690Stephen G. Gaffney, Jeffrey P. Townsend. PathScore: a web tool for identifying altered pathways in cancer data
3691 -- 3693Jan R. Detrez, Jean-Marie Vanderwinden, Michaël Barbier, Marlies Verschuuren, Rony Nuydens, Xavier Langlois, Jean-Pierre Timmermans, Winnok De Vos. BiDiFuse: a FIJI plugin for fusing bi-directionally recorded microscopic image volumes
3694 -- 0X. Hu, Q. Dong, J. Yang, Y. Zhang. ab initio modeling with template-based transferals

Volume 32, Issue 22

3375 -- 3379Sebastián Duchêne, Jemma L. Geoghegan, Edward C. Holmes, Simon Y. W. Ho. Estimating evolutionary rates using time-structured data: a general comparison of phylogenetic methods
3380 -- 3387Dmitry Antipov, Nolan Hartwick, Max Shen, Mikhail Raiko, Alla Lapidus, Pavel A. Pevzner. plasmidSPAdes: assembling plasmids from whole genome sequencing data
3388 -- 3395Stefanie König, Lars Romoth, Lizzy Gerischer, Mario Stanke. Simultaneous gene finding in multiple genomes
3396 -- 3404Yalu Wen, Fushun Chen, Qingzheng Zhang, Yan Zhuang, Zhiguang Li. Detection of differentially methylated regions in whole genome bisulfite sequencing data using local Getis-Ord statistics
3405 -- 3412Subrata Saha, Sanguthevar Rajasekaran. NRGC: a novel referential genome compression algorithm
3413 -- 3419Véronique Hourdel, Stevenn Volant, Darragh P. O'Brien, Alexandre Chenal, Julia Chamot-Rooke, Marie-Agnès Dillies, Sébastien Brier. MEMHDX: an interactive tool to expedite the statistical validation and visualization of large HDX-MS datasets
3420 -- 3427George A. Cortina, Peter M. Kasson. Excess positional mutual information predicts both local and allosteric mutations affecting beta lactamase drug resistance
3428 -- 3434Mengyin Lu, Matthew Stephens. vash): flexible empirical Bayes estimation of variances
3435 -- 3443Yun Hao, Nicholas P. Tatonetti. Predicting G protein-coupled receptor downstream signaling by tissue expression
3444 -- 3453Zhehuan Zhao, Zhihao Yang, Ling Luo, Hongfei Lin, Jian Wang. Drug drug interaction extraction from biomedical literature using syntax convolutional neural network
3454 -- 3460Shu Tadaka, Kengo Kinoshita. NCMine: Core-peripheral based functional module detection using near-clique mining
3461 -- 3468Daniyar Bakirov, Alex Pappachen James, Amin Zollanvari. An efficient method to estimate the optimum regularization parameter in RLDA
3469 -- 3470Yi Wang, Ling Xu, Yong Qiang Gu, Devin Coleman-Derr. MetaCoMET: a web platform for discovery and visualization of the core microbiome
3471 -- 3479Yukako Tohsato, Kenneth H. L. Ho, Koji Kyoda, Shuichi Onami. SSBD: a database of quantitative data of spatiotemporal dynamics of biological phenomena
3480 -- 3488Jian Fang, Dongdong Lin, S. Charles Schulz, ZongBen Xu, Vince D. Calhoun, Yu-Ping Wang. Joint sparse canonical correlation analysis for detecting differential imaging genetics modules
3489 -- 3491Samuele Bovo, Pietro di Lena, Pier Luigi Martelli, Piero Fariselli, Rita Casadio. NET-GE: a web-server for NETwork-based human gene enrichment
3492 -- 3494Hamid Mohamadi, Justin Chu, Benjamin P. Vandervalk, Inanç Birol. ntHash: recursive nucleotide hashing
3495 -- 3497Qiang Kou, Likun Xun, Xiaowen Liu. TopPIC: a software tool for top-down mass spectrometry-based proteoform identification and characterization
3498 -- 3500Chia-Hua Chang, Min-Te Chou, Yi-Chung Wu, Ting-Wei Hong, Yun-Lung Li, Chia-Hsiang Yang, Jui-Hung Hung. sBWT: memory efficient implementation of the hardware-acceleration-friendly Schindler transform for the fast biological sequence mapping
3501 -- 3503Guy Yachdav, Sebastian Wilzbach, Benedikt Rauscher, Robert Sheridan, Ian Sillitoe, James B. Procter, Suzanna E. Lewis, Burkhard Rost, Tatyana Goldberg. MSAViewer: interactive JavaScript visualization of multiple sequence alignments
3504 -- 3506Samuel A. Lambert, Mihai Albu, Timothy R. Hughes, Hamed Shateri Najafabadi. Motif comparison based on similarity of binding affinity profiles
3507 -- 3509Haifeng Chen, Andrew D. Smith, Ting Chen. WALT: fast and accurate read mapping for bisulfite sequencing
3510 -- 3512Lars Skjærven, Shashank Jariwala, Xin-Qiu Yao, Barry J. Grant. Online interactive analysis of protein structure ensembles with Bio3D-web
3513 -- 3515Aika Terada, Ryo Yamada, Koji Tsuda, Jun Sese. LAMPLINK: detection of statistically significant SNP combinations from GWAS data
3516 -- 3518Diego Ortega-Del Vecchyo, Clare D. Marsden, Kirk E. Lohmueller. PReFerSim: fast simulation of demography and selection under the Poisson Random Field model
3519 -- 3521Giovanni Stracquadanio, Kun Yang, Jef D. Boeke, Joel S. Bader. BioPartsDB: a synthetic biology workflow web-application for education and research
3522 -- 3524Tadi Venkata Sivakumar, Varun Giri, Jin Hwan Park, Tae-Yong Kim, Anirban Bhaduri. ReactPRED: a tool to predict and analyze biochemical reactions
3525 -- 3527Richard A. Schäfer, Björn Voß. VisualGraphX: interactive graph visualization within Galaxy
3528 -- 3529Li Chen, Yongyi Yu, Xinchen Zhang, Chen Liu, Chuyu Ye, Longjiang Fan. PcircRNA_finder: a software for circRNA prediction in plants
3530 -- 3531Mark R. Winter, Walter C. Mankowski, Eric Wait, Sally Temple, Andrew R. Cohen. LEVER: software tools for segmentation, tracking and lineaging of proliferating cells
3532 -- 3534David Legland, Ignacio Arganda-Carreras, Philippe Andrey. MorphoLibJ: integrated library and plugins for mathematical morphology with ImageJ

Volume 32, Issue 21

3215 -- 3223Sara El-Metwally, Magdi Zakaria, Taher Hamza. LightAssembler: fast and memory-efficient assembly algorithm for high-throughput sequencing reads
3224 -- 3232Bo Liu, Hongzhe Guo, Michael Brudno, Yadong Wang. deBGA: read alignment with de Bruijn graph-based seed and extension
3233 -- 3239Qamar M. Sheikh, Derek Gatherer, Pedro A. Reche, Darren R. Flower. Towards the knowledge-based design of universal influenza epitope ensemble vaccines
3240 -- 3245Gongyi Huang, Shaoli Wang, Xueqin Wang, Na You. An empirical Bayes method for genotyping and SNP detection using multi-sample next-generation sequencing data
3246 -- 3251Kazunori Yamada, Kentaro Tomii, Kazutaka Katoh. Application of the MAFFT sequence alignment program to large data - reexamination of the usefulness of chained guide trees
3252 -- 3259Marco Barsacchi, Eva Maria Novoa, Manolis Kellis, Alessio Bechini. SwiSpot: modeling riboswitches by spotting out switching sequences
3260 -- 3269Xiuzhen Hu, Qiwen Dong, Jianyi Yang, Yang Zhang. ab initio modeling with template-based transferals
3270 -- 3278Pawel Krupa, Magdalena A. Mozolewska, Marta Wisniewska, Yanping Yin, Yi He, Adam K. Sieradzan, Robert Ganzynkowicz, Agnieszka G. Lipska, Agnieszka Karczynska, Magdalena Slusarz, Rafal Slusarz, Artur Gieldon, Cezary Czaplewski, Dawid Jagiela, Bartlomiej Zaborowski, Harold A. Scheraga, Adam Liwo. Performance of protein-structure predictions with the physics-based UNRES force field in CASP11
3279 -- 3290Xuebei An, Jianhua Hu, Kim-Anh Do. SIFORM: shared informative factor models for integration of multi-platform bioinformatic data
3291 -- 3297Zhi Liu, Tuantuan Gui, Zhen Wang, Hong Li, Yunhe Fu, Xiao Dong, Yixue Li. cis-regulated allele-specific expression in RNA sequencing data
3298 -- 3305A. Macé, M. A. Tuke, J. S. Beckmann, L. Lin, S. Jacquemont, M. N. Weedon, A. Reymond, Z. Kutalik. New quality measure for SNP array based CNV detection
3306 -- 3313Yat Hin Chan, Jukka Intosalmi, Sini Rautio, Harri Lähdesmäki. A subpopulation model to analyze heterogeneous cell differentiation dynamics
3314 -- 3320Tomer Illouz, Ravit Madar, Charlotte Clague, Kathleen J. Griffioen, Yoram Louzoun, Eitan Okun. Unbiased classification of spatial strategies in the Barnes maze
3321 -- 3323Alla Mikheenko, Gleb Valin, Andrey D. Prjibelski, Vladislav Saveliev, Alexey A. Gurevich. de novo assembly evaluation
3324 -- 3326Hamid Younesy, Cydney B. Nielsen, Matthew C. Lorincz, Steven J. M. Jones, Mohammad M. Karimi, Torsten Möller. ChAsE: chromatin analysis and exploration tool
3327 -- 3329Thomas Weinmaier, Alexander Platzer, Jeroen Frank, Hans-Jörg Hellinger, Patrick Tischler, Thomas Rattei. ConsPred: a rule-based (re-)annotation framework for prokaryotic genomes
3330 -- 3332Jakob Dohrmann, Rahul Singh. The SMAL web server: global multiple network alignment from pairwise alignments
3333 -- 3335Mingyang Cai, Fan Gao, Wange Lu, Kai Wang. w4CSeq: software and web application to analyze 4C-seq data
3336 -- 3338Jian Ma, Johannes Köster, Qian Qin, Shengen Hu, Wei Li, Chenhao Chen, Qingyi Cao, Jinzeng Wang, Shenglin Mei, Qi Liu, Han Xu, Xiaole Shirley Liu. CRISPR-DO for genome-wide CRISPR design and optimization
3339 -- 3341Altan Kara, Martin J. Vickers, Martin T. Swain, David E. Whitworth, Narcis Fernandez-Fuentes. MetaPred2CS: a sequence-based meta-predictor for protein-protein interactions of prokaryotic two-component system proteins
3342 -- 3344Bing Xia, Sandor Vajda, Dima Kozakov. Accounting for pairwise distance restraints in FFT-based protein-protein docking
3345 -- 3347Alexey Stupnikov, Shailesh Tripathi, Ricardo de Matos Simoes, Darragh G. McArt, Manuel Salto-Tellez, Galina V. Glazko, Matthias Dehmer, Frank Emmert-Streib. samExploreR: exploring reproducibility and robustness of RNA-seq results based on SAM files
3348 -- 3350Xiaoyu Wang, James Y. Dai. TwoPhaseInd: an R package for estimating gene-treatment interactions and discovering predictive markers in randomized clinical trials
3351 -- 3353Gang Wu, Ron C. Anafi, Michael Hughes, Karl Kornacker, John B. Hogenesch. MetaCycle: an integrated R package to evaluate periodicity in large scale data
3354 -- 3356Guillaume Devailly, Anna Mantsoki, Anagha Joshi. Heat*seq: an interactive web tool for high-throughput sequencing experiment comparison with public data
3357 -- 3359Eva Balsa-Canto, David Henriques, Attila Gábor, Julio R. Banga. AMIGO2, a toolbox for dynamic modeling, optimization and control in systems biology
3360 -- 3362Irene Otero-Muras, David Henriques, Julio R. Banga. SYNBADm: a tool for optimization-based automated design of synthetic gene circuits
3363 -- 3365David G. P. van IJzendoorn, Kimberly Glass, John Quackenbush, Marieke L. Kuijjer. PyPanda: a Python package for gene regulatory network reconstruction
3366 -- 3368Leonard A. Harris, Justin S. Hogg, José Juan Tapia, John A. P. Sekar, Sanjana Gupta, Ilya Korsunsky, Arshi Arora, Dipak Barua, Robert P. Sheehan, James R. Faeder. BioNetGen 2.2: advances in rule-based modeling
3369 -- 3370Maureen R. Smith, Redmond P. Smyth, Roland Marquet, Max von Kleist. MIMEAnTo: profiling functional RNA in mutational interference mapping experiments
3371 -- 3373Edgar Mixcoha, Roberto Rosende, Rebeca García-Fandiño, Ángel Piñeiro. Cyclo-lib: a database of computational molecular dynamics simulations of cyclodextrins

Volume 32, Issue 20

3053 -- 3057Anna A. Deeva, Evgenia A. Temlyakova, Anatoly A. Sorokin, Elena V. Nemtseva, Valentina A. Kratasyuk. Structural distinctions of fast and slow bacterial luciferases revealed by phylogenetic analysis
3058 -- 3064Jianwei Zhang, Dave Kudrna, Ting Mu, Weiming Li, Dario Copetti, Yeisoo Yu, Jose Luis Goicoechea, Yang Lei, Rod A. Wing. Genome puzzle master (GPM): an integrated pipeline for building and editing pseudomolecules from fragmented sequences
3065 -- 3071Jacob Shujui Hsu, Johnny S. H. Kwan, Zhicheng Pan, Maria-Mercè Garcia-Barcelo, Pak Chung Sham, Miao-Xin Li. Inheritance-mode specific pathogenicity prioritization (ISPP) for human protein coding genes
3072 -- 3080Junho Kim, Ju Heon Maeng, Jae Seok Lim, Hyeonju Son, JuneHawk Lee, Jeong Ho Lee, Sangwoo Kim. Vecuum: identification and filtration of false somatic variants caused by recombinant vector contamination
3081 -- 3088Hákon Guðbjartsson, Guðmundur Fr. Georgsson, Sigurjón Axel Guðjónsson, Ragnar þór Valdimarsson, Jóhann H. Sigurðsson, Sigmar K. Stefánsson, Gísli Másson, Gísli Magnússon, Vilmundur Pálmason, Kári Stefánsson. GORpipe: a query tool for working with sequence data based on a Genomic Ordered Relational (GOR) architecture
3089 -- 3097John P. Barton, Eleonora De Leonardis, Alice Coucke, Simona Cocco. ACE: adaptive cluster expansion for maximum entropy graphical model inference
3098 -- 3106Bram Gerritsen, Aridaman Pandit, Arno C. Andeweg, Rob J. De Boer. RTCR: a pipeline for complete and accurate recovery of T cell repertoires from high throughput sequencing data
3107 -- 3115Ping-Ping Wen, Shao-Ping Shi, Hao-Dong Xu, Li-na Wang, Jian-Ding Qiu. in silico prediction of species-specific methylation sites based on information gain feature optimization
3116 -- 3123Wangren Qiu, Bi-Qian Sun, Xuan Xiao, Zhao-Chun Xu, Kuo-Chen Chou. iPTM-mLys: identifying multiple lysine PTM sites and their different types
3124 -- 3132Daniel L. Greenfield, Oliver Stegle, Alban Rrustemi. GeneCodeq: quality score compression and improved genotyping using a Bayesian framework
3133 -- 3141Jianhua Jia, Liuxia Zhang, Zi Liu, Xuan Xiao, Kuo-Chen Chou. pSumo-CD: predicting sumoylation sites in proteins with covariance discriminant algorithm by incorporating sequence-coupled effects into general PseAAC
3142 -- 3149Pradeep Anand Ravindranath, Michel F. Sanner. AutoSite: an automated approach for pseudo-ligands prediction - from ligand-binding sites identification to predicting key ligand atoms
3150 -- 3154Haixiang Zhang, Yinan Zheng, Zhou Zhang, Tao Gao, Brian Joyce, Grace Yoon, Wei Zhang, Joel Schwartz, Allan Just, Elena Colicino, Pantel Vokonas, Lihui Zhao, Jinchi Lv, Andrea A. Baccarelli, Lifang Hou, Lei Liu. Estimating and testing high-dimensional mediation effects in epigenetic studies
3155 -- 3164Lei Meng, Aaron Striegel, Tijana Milenkovic. Local versus global biological network alignment
3165 -- 3174Jing Ma, Ali Shojaie, George Michailidis. Network-based pathway enrichment analysis with incomplete network information
3175 -- 3182Dhanya Sridhar, Shobeir Fakhraei, Lise Getoor. A probabilistic approach for collective similarity-based drug-drug interaction prediction
3183 -- 3189Na Le Dang, Tyler B. Hughes, Varun Krishnamurthy, S. Joshua Swamidass. A simple model predicts UGT-mediated metabolism
3190 -- 3192Kai Kruse, Clemens B. Hug, Benjamín Hernández-Rodríguez, Juan M. Vaquerizas. TADtool: visual parameter identification for TAD-calling algorithms
3193 -- 3195Bai-Han Zhu, Ying-Nan Song, Wei Xue, Gui-Cai Xu, Jun Xiao, Ming-Yuan Sun, Xiaowen Sun, Jiongtang Li. PEP_scaffolder: using (homologous) proteins to scaffold genomes
3196 -- 3198Ewa A. Bergmann, Bo-Juen Chen, Kanika Arora, Vladimir Vacic, Michael C. Zody. Conpair: concordance and contamination estimator for matched tumor-normal pairs
3199 -- 3200Vittorio Fortino, Roberto Tagliaferri, Dario Greco. CONDOP: an R package for CONdition-Dependent Operon Predictions
3201 -- 3203Steffi Grote, Kay Prüfer, Janet Kelso, Michael Dannemann. ABAEnrichment: an R package to test for gene set expression enrichment in the adult and developing human brain
3204 -- 3206Simon Dellicour, Rebecca Rose, Nuno R. Faria, Philippe Lemey, Oliver G. Pybus. SERAPHIM: studying environmental rasters and phylogenetically informed movements
3207 -- 3209James R. Staley, James A. Blackshaw, Mihir A. Kamat, Steve Ellis, Praveen Surendran, Benjamin B. Sun, Dirk S. Paul, Daniel Freitag, Stephen Burgess, John Danesh, Robin Young, Adam S. Butterworth. PhenoScanner: a database of human genotype-phenotype associations
3210 -- 3212David Dao, Adam Fraser, Jane Hung, Vebjorn Ljosa, Shantanu Singh, Anne E. Carpenter. CellProfiler Analyst: interactive data exploration, analysis and classification of large biological image sets
3213 -- 0Vikas Bansal, Vikas Bansal, Ondrej Libiger. A statistical method for the detection of variants from next-generation resequencing of DNA poolsA probabilistic method for the detection and genotyping of small indels from population-scale sequence data

Volume 32, Issue 2

161 -- 164J. Caroli, Cristian Taccioli, A. De La Fuente, P. Serafini, Silvio Bicciato. APTANI: a computational tool to select aptamers through sequence-structure motif analysis of HT-SELEX data
165 -- 172Van-Minh Bui, Cheng-Tsung Lu, Thi-Trang Ho, Tzong-Yi Lee. S-sulfenylation sites with substrate motifs
173 -- 180Zhiying Wang, Tsachy Weissman, Olgica Milenkovic. smallWig: parallel compression of RNA-seq WIG files
181 -- 186Bernhard Knapp, Samuel Demharter, Charlotte M. Deane, Peter Minary. Exploring peptide/MHC detachment processes using hierarchical natural move Monte Carlo
187 -- 194Marcel Kucharík, Ivo L. Hofacker, Peter F. Stadler, Jing Qin. Pseudoknots in RNA folding landscapes
195 -- 202Thomas J. Hardcastle. Generalized empirical Bayesian methods for discovery of differential data in high-throughput biology
203 -- 210Recep Colak, Taehyung Kim, Hilal Kazan, Yoomi Oh, Miguel Cruz, Adan Valladares-Salgado, Jesus Peralta, Jorge Escobedo, Esteban J. Parra, Philip M. Kim, Anna Goldenberg. JBASE: Joint Bayesian Analysis of Subphenotypes and Epistasis
211 -- 218Shuang Wang, Yuchen Zhang, Wenrui Dai, Kristin E. Lauter, Miran Kim, Yuzhe Tang, Hongkai Xiong, Xiaoqian Jiang. HEALER: homomorphic computation of ExAct Logistic rEgRession for secure rare disease variants analysis in GWAS
219 -- 225Miquel Marin-Riera, Miguel Brun-Usan, Roland Zimm, Tommi Välikangas, Isaac Salazar-Ciudad. Computational modeling of development by epithelia, mesenchyme and their interactions: a unified model
226 -- 234Yong-Cui Wang, Shi-Long Chen, Nai-Yang Deng, Yong Wang. Computational probing protein-protein interactions targeting small molecules
235 -- 241Francesco Napolitano, Francesco Sirci, Diego Carrella, Diego di Bernardo. Drug-set enrichment analysis: a novel tool to investigate drug mode of action
242 -- 251Allison N. Tegge, Nicholas Sharp, T. M. Murali. Xtalk: a path-based approach for identifying crosstalk between signaling pathways
252 -- 259Pengyi Yang, Sean J. Humphrey, David E. James, Yee Hwa Yang, Raja Jothi. Positive-unlabeled ensemble learning for kinase substrate prediction from dynamic phosphoproteomics data
260 -- 267Jiyang Yu, Jose Silva, Andrea Califano. ScreenBEAM: a novel meta-analysis algorithm for functional genomics screens via Bayesian hierarchical modeling
268 -- 275Nathaniel G. Mahieu, Jonathan L. Spalding, Gary J. Patti. Warpgroup: increased precision of metabolomic data processing by consensus integration bound analysis
276 -- 282Suwisa Kaewphan, Sofie Van Landeghem, Tomoko Ohta, Yves Van de Peer, Filip Ginter, Sampo Pyysalo. Cell line name recognition in support of the identification of synthetic lethality in cancer from text
283 -- 285Tomaz Berisa, Joseph K. Pickrell. Approximately independent linkage disequilibrium blocks in human populations
286 -- 288Belinda Phipson, Jovana Maksimovic, Alicia Oshlack. missMethyl: an R package for analyzing data from Illumina's HumanMethylation450 platform
289 -- 291Bernat Gel, Anna Díez-Villanueva, Eduard Serra, Marcus Buschbeck, Miguel A. Peinado, Roberto Malinverni. regioneR: an R/Bioconductor package for the association analysis of genomic regions based on permutation tests
292 -- 294Konstantin Okonechnikov, Ana Conesa, Fernando García-Alcalde. Qualimap 2: advanced multi-sample quality control for high-throughput sequencing data
295 -- 297Donghyung Lee, Vernell S. Williamson, T. Bernard Bigdeli, Brien P. Riley, Bradley T. Webb, Ayman H. Fanous, Kenneth S. Kendler, Vladimir I. Vladimirov, Silviu-Alin Bacanu. JEPEGMIX: gene-level joint analysis of functional SNPs in cosmopolitan cohorts
298 -- 300James Dunbar, Charlotte M. Deane. ANARCI: antigen receptor numbering and receptor classification
301 -- 303Paul Hodor, Amandeep Chawla, Andrew Clark, Lauren Neal. cl-dash: rapid configuration and deployment of Hadoop clusters for bioinformatics research in the cloud
304 -- 305Sergey Sheetlin, Yonil Park, Martin C. Frith, John L. Spouge. E-values
306 -- 308Devin K. Schweppe, Juan D. Chavez, James E. Bruce. XLmap: an R package to visualize and score protein structure models based on sites of protein cross-linking
309 -- 311Max Franz, Christian Tannus Lopes, Gerardo Huck, Yue Dong, Selçuk Onur Sümer, Gary D. Bader. Cytoscape.js: a graph theory library for visualisation and analysis
312 -- 314James M. Melott, John N. Weinstein, Bradley M. Broom. PathwaysWeb: a gene pathways API with directional interactions, expanded gene ontology, and versioning
315 -- 317Andreas Bartschat, Eduard Hübner, Markus Reischl, Ralf Mikut, Johannes Stegmaier. XPIWIT - an XML pipeline wrapper for the Insight Toolkit
318 -- 320Pavel Krízek, Tomás Lukes, Martin Ovesný, Karel Fliegel, Guy M. Hagen. SIMToolbox: a MATLAB toolbox for structured illumination fluorescence microscopy

Volume 32, Issue 19

2891 -- 2895Zijian Ding, Songpeng Zu, Jin Gu. Evaluating the molecule-based prediction of clinical drug responses in cancer
2896 -- 2902Pol Cuscó, Guillaume J. Filion. Zerone: a ChIP-seq discretizer for multiple replicates with built-in quality control
2903 -- 2910Micol Marchetti-Bowick, Junming Yin, Judie A. Howrylak, Eric P. Xing. A time-varying group sparse additive model for genome-wide association studies of dynamic complex traits
2911 -- 2919Yuta Suzuki, Jonas Korlach, Stephen W. Turner, Tatsuya Tsukahara, Junko Taniguchi, Wei Qu, Kazuki Ichikawa, Jun Yoshimura, Hideaki Yurino, Yuji Takahashi, Jun Mitsui, Hiroyuki Ishiura, Shoji Tsuji, Hiroyuki Takeda, Shinichi Morishita. AgIn: measuring the landscape of CpG methylation of individual repetitive elements
2920 -- 2927Panu Somervuo, Sonja Koskela, Juho Pennanen, R. Henrik Nilsson, Otso Ovaskainen. Unbiased probabilistic taxonomic classification for DNA barcoding
2928 -- 2935Markus Fricke, Manja Marz. Prediction of conserved long-range RNA-RNA interactions in full viral genomes
2936 -- 2946Lijun Quan, Qiang Lv, Yang Zhang. STRUM: structure-based prediction of protein stability changes upon single-point mutation
2947 -- 2955Nouf S. Al-Numair, Luis Lopes, Petros Syrris, Lorenzo Monserrat, Perry Elliott, Andrew C. R. Martin. The structural effects of mutations can aid in differential phenotype prediction of beta-myosin heavy chain (Myosin-7) missense variants
2956 -- 2964Jing Yang, Christopher A. Penfold, Murray R. Grant, Magnus Rattray. Inferring the perturbation time from biological time course data
2965 -- 2972Yuanhua Huang, Guido Sanguinetti. Statistical modeling of isoform splicing dynamics from RNA-seq time series data
2973 -- 2980John E. Reid, Lorenz Wernisch. Pseudotime estimation: deconfounding single cell time series
2981 -- 2987Kun Ming Kenneth Lim, Chenhao Li, Kern Rei Chng, Niranjan Nagarajan. @MInter: automated text-mining of microbial interactions
2988 -- 2995Fábio Fabris, Alex Alves Freitas. New KEGG pathway-based interpretable features for classifying ageing-related mouse proteins
2996 -- 3004Guangyuan Fu, Jun Wang, Bo Yang, Guo-Xian Yu. NegGOA: negative GO annotations selection using ontology structure
3005 -- 3011Christopher B. Barnett, Kiyoko F. Aoki-Kinoshita, Kevin J. Naidoo. The Glycome Analytics Platform: an integrative framework for glycobioinformatics
3012 -- 3014Zachary L. Skidmore, Alex H. Wagner, Robert Lesurf, Katie M. Campbell, Jason Kunisaki, Obi L. Griffith, Malachi Griffith. GenVisR: Genomic Visualizations in R
3015 -- 3017F. Anthony San Lucas, Smruthy Sivakumar, Selina Vattathil, Jerry Fowler, Eduardo VilarE. Vilar, Paul Scheet. hapLOHseq
3018 -- 3020Tomasz Stokowy, Mateusz Garbulowski, Torunn Fiskerstrand, Rita Holdhus, Kornel Labun, Pawel Sztromwasser, Christian Gilissen, Alexander Hoischen, Gunnar Houge, Kjell Petersen, Inge Jonassen, Vidar M. Steen. RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data
3021 -- 3023Maria Nattestad, Michael C. Schatz. Assemblytics: a web analytics tool for the detection of variants from an assembly
3024 -- 3026Zhong Wang, André L. Martins, Charles G. Danko. RTFBSDB: an integrated framework for transcription factor binding site analysis
3027 -- 3028Astrid Cruaud, Mathieu Gautier, Jean-Pierre Rossi, Jean-Yves Rasplus, Jérôme Gouzy. RAD-seq data for interspecific phylogeny
3029 -- 3031Billy Heung Wing Chang, Weidong Tian. GSA-Lightning: ultra-fast permutation-based gene set analysis
3032 -- 3034Pier Francesco Palamara. ARGON: fast, whole-genome simulation of the discrete time Wright-fisher process
3035 -- 3037Russell Corbett-Detig, Matt Jones. SELAM: simulation of epistasis and local adaptation during admixture with mate choice
3038 -- 3040Daniel Edsgärd, Björn Reinius, Rickard Sandberg. scphaser: haplotype inference using single-cell RNA-seq data
3041 -- 3043Francisco Salavert, Luz Garcia-Alonso, Rubén Sánchez, Roberto Alonso, Marta Bleda, Ignacio Medina, Joaquín Dopazo. Web-based network analysis and visualization using CellMaps
3044 -- 3046Sun Kim, Lana Yeganova, W. John Wilbur. Meshable: searching PubMed abstracts by utilizing MeSH and MeSH-derived topical terms
3047 -- 3048Philip Ewels, Måns Magnusson, Sverker Lundin, Max Käller. MultiQC: summarize analysis results for multiple tools and samples in a single report
3049 -- 3050Vijay Barve, Javier Otegui. bdvis: visualizing biodiversity data in R
3051 -- 0Forest Agostinelli, Nicholas Ceglia, Babak Shahbaba, Paolo Sassone-Corsi, Pierre Baldi. What time is it? Deep learning approaches for circadian rhythms

Volume 32, Issue 18

2729 -- 2736Mulin Jun Li, Zhicheng Pan, Zipeng Liu, Jiexing Wu, Panwen Wang, Yun Zhu, Feng Xu, Zhengyuan Xia, Pak Chung Sham, Jean-Pierre A. Kocher, Miao-Xin Li, Jun S. Liu, Junwen Wang. Predicting regulatory variants with composite statistic
2737 -- 2743Xiaonan Hu, Wei Zhang, Sanguo Zhang, Shuangge Ma, Qizhai Li. P-values with applications to genetic association studies
2744 -- 2752Mindaugas Margelevicius. Bayesian nonparametrics in protein remote homology search
2753 -- 2759Kira Vyatkina, Si Wu, Lennard J. Dekker, Martijn M. VanDuijn, Xiaowen Liu, Nikola Tolic, Theo M. Luider, Ljiljana Pasa-Tolic, Pavel A. Pevzner. de novo sequencing techniques
2760 -- 2767Vladimir Ulyantsev, Sergey Kazakov, Veronika B. Dubinkina, Alexander V. Tyakht, Dmitry G. Alexeev. MetaFast: fast reference-free graph-based comparison of shotgun metagenomic data
2768 -- 2775Jun Ding, Xiaoman Li, Haiyan Hu. TarPmiR: a new approach for microRNA target site prediction
2776 -- 2782Thomas Hrabe, Lukasz Jaroszewski, Adam Godzik. Revealing aperiodic aspects of solenoid proteins from sequence information
2783 -- 2790Abdullah Al Mamun, Soumitra Pal 0001, Sanguthevar Rajasekaran. k-mer Counter based on Multiple Burst Trees
2791 -- 2799Debswapna Bhattacharya, Renzhi Cao, Jianlin Cheng. de novo protein structure prediction using united-residue conformational search via stepwise, probabilistic sampling
2800 -- 2808Paul Florian Thaben, Pål O. Westermark. Differential rhythmicity: detecting altered rhythmicity in biological data
2809 -- 2816Francisco García-García, Joaquin Panadero, Joaquín Dopazo, David Montaner. Integrated gene set analysis for microRNA studies
2817 -- 2823Aaron A. Behr, Katherine Z. Liu, Gracie Liu-Fang, Priyanka Nakka, Sohini Ramachandran. pong: fast analysis and visualization of latent clusters in population genetic data
2824 -- 2830Jung Eun Shim, Insuk Lee. Weighted mutual information analysis substantially improves domain-based functional network models
2831 -- 2838Hongyi Zhou, Jeffrey Skolnick. A knowledge-based approach for predicting gene-disease associations
2839 -- 2846Robert Leaman, Zhiyong Lu. TaggerOne: joint named entity recognition and normalization with semi-Markov Models
2847 -- 2849Zuguang Gu, Roland Eils, Matthias Schlesner. Complex heatmaps reveal patterns and correlations in multidimensional genomic data
2850 -- 2852Yana Valasatava, Antonio Rosato, Lucia Banci, Claudia Andreini. MetalPredator: a web server to predict iron-sulfur cluster binding proteomes
2853 -- 2855Shravan Sukumar, Xiaolei Zhu, Spencer S. Ericksen, Julie C. Mitchell. DBSI server: DNA binding site identifier
2856 -- 2857Umesh K. Nandal, Antoine H. C. van Kampen, Perry D. Moerland. compendiumdb: an R package for retrieval and storage of functional genomics data
2858 -- 2860David J. Arenillas, Alistair R. R. Forrest, Hideya Kawaji, Timo Lassmann, Wyeth W. Wasserman, Anthony Mathelier. CAGEd-oPOSSUM: motif enrichment analysis from CAGE-derived TSSs
2861 -- 2862Yuri Tani Utsunomiya, Marco Milanesi, Adam T. H. Utsunomiya, Paolo Ajmone-Marsan, José Fernando Garcia. GHap: an R package for genome-wide haplotyping
2863 -- 2865Sisi Fan, Quentin Geissmann, Eszter Lakatos, Saulius Lukauskas, Angelique Ale, Ann C. Babtie, Paul D. W. Kirk, Michael P. H. Stumpf. MEANS: python package for Moment Expansion Approximation, iNference and Simulation
2866 -- 2868Giovanni Y. Di Veroli, Chiara Fornari, Dennis Wang, Séverine Mollard, Jo L. Bramhall, Frances M. Richards, Duncan I. Jodrell. Combenefit: an interactive platform for the analysis and visualization of drug combinations
2869 -- 2871Samy Deghou, Georg Zeller, Murat Iskar, Marja Driessen, Mercedes Castillo, Vera van Noort, Peer Bork. CART - a chemical annotation retrieval toolkit
2872 -- 2874Giorgio Valentini, Giuliano Armano, Marco Frasca, Jianyi Lin, Marco Mesiti, Matteo Re. RANKS: a flexible tool for node label ranking and classification in biological networks
2875 -- 2876Daniel Weindl, André Wegner, Karsten Hiller. MIA: non-targeted mass isotopolome analysis
2877 -- 2879Michael J. O'Connell, Eric F. Lock. R.JIVE for exploration of multi-source molecular data
2880 -- 2882James C. Schaff, Dan Vasilescu, Ion I. Moraru, Leslie M. Loew, Michael L. Blinov. Rule-based modeling with Virtual Cell
2883 -- 2885Philippe E. Thomas, Tim Rocktäschel, Jörg Hakenberg, Yvonne Lichtblau, Ulf Leser. SETH detects and normalizes genetic variants in text
2886 -- 2888Kyubum Lee, Won-Ho Shin, Byounggun Kim, Sunwon Lee, Yonghwa Choi, Sunkyu Kim, Minji Jeon, Aik Choon Tan, Jaewoo Kang. HiPub: translating PubMed and PMC texts to networks for knowledge discovery
2889 -- 0Sayoni Das, David A. Lee, Ian Sillitoe, Natalie L. Dawson, Jonathan G. Lees, Christine A. Orengo. Functional classification of CATH superfamilies: a domain-based approach for protein function annotation

Volume 32, Issue 17

389 -- 392Jaap Heringa, Marcel J. T. Reinders, Sanne Abeln, Jeroen de Ridder. ECCB 2016: The 15th European Conference on Computational Biology
396 -- 404Michael Lenz, Nadia J. T. Roumans, Roel G. Vink, Marleen A. van Baak, Edwin C. M. Mariman, Ilja C. W. Arts, Theo M. de Kok, Gökhan Ertaylan. Estimating real cell size distribution from cross-section microscopy imaging
405 -- 412Chantriolnt-Andreas Kapourani, Guido Sanguinetti. Higher order methylation features for clustering and prediction in epigenomic studies
413 -- 420Nanne Aben, Daniel J. Vis, Magali Michaut, Lodewyk F. A. Wessels. TANDEM: a two-stage approach to maximize interpretability of drug response models based on multiple molecular data types
421 -- 429Charles J. Labuzzetta, Margaret L. Antonio, Patricia M. Watson, Robert C. Wilson, Lauren A. Laboissonniere, Jeffrey M. Trimarchi, Baris Genc, P. Hande Ozdinler, Dennis K. Watson, Paul E. Anderson. Complementary feature selection from alternative splicing events and gene expression for phenotype prediction
430 -- 436William Poole, David L. Gibbs, Ilya Shmulevich, Brady Bernard, Theo A. Knijnenburg. P-values with an empirical adaptation of Brown's method
437 -- 444Sunjoo Bang, Jae-Hoon Kim, Hyunjung Shin. Causality modeling for directed disease network
445 -- 454Thanh Le Van, Matthijs van Leeuwen, Ana Carolina Fierro, Dries De Maeyer, Jimmy Van den Eynden, Lieven P. C. Verbeke, Luc De Raedt, Kathleen Marchal, Siegfried Nijssen. Simultaneous discovery of cancer subtypes and subtype features by molecular data integration
455 -- 463Muhammad Ammad-ud-din, Suleiman A. Khan, Disha Malani, Astrid Murumägi, Olli-P. Kallioniemi, Tero Aittokallio, Samuel Kaski. Drug response prediction by inferring pathway-response associations with kernelized Bayesian matrix factorization
464 -- 472Dalia Cohn-Alperovich, Alona Rabner, Ilona Kifer, Yael Mandel-Gutfreund, Zohar Yakhini. Mutual enrichment in aggregated ranked lists with applications to gene expression regulation
473 -- 478Georg Summer, Thomas Kelder, Marijana Radonjic, Marc van Bilsen, Suzan Wopereis, Stephane Heymans. The Network Library: a framework to rapidly integrate network biology resources
479 -- 486Kedar Tatwawadi, Mikel Hernaez, Idoia Ochoa, Tsachy Weissman. GTRAC: fast retrieval from compressed collections of genomic variants
487 -- 493Siavash Sheikhizadeh, M. Eric Schranz, Mehmet Akdel, Dick de Ridder, Sandra Smit. PanTools: representation, storage and exploration of pan-genomic data
494 -- 502Ilan Shomorony, Samuel H. Kim, Thomas A. Courtade, David N. C. Tse. Information-optimal genome assembly via sparse read-overlap graphs
503 -- 510Andreas D. M. Gunawan, Bingxin Lu, Louxin Zhang. A program for verification of phylogenetic network models
511 -- 519Tarmo Äijö, Xiaojing Yue, Anjana Rao, Harri Lähdesmäki. LuxGLM: a probabilistic covariate model for quantification of DNA methylation modifications with complex experimental designs
520 -- 528Jikai Lei, Yanni Sun. Assemble CRISPRs from metagenomic sequencing data
529 -- 537Nan Du, Yanni Sun. Improve homology search sensitivity of PacBio data by correcting frameshifts
538 -- 544Ariya Shajii, Deniz Yörükoglu, Yun William Yu, Bonnie Berger. k-mer matching
545 -- 551Ehsan Haghshenas, Faraz Hach, Süleyman Cenk Sahinalp, Cédric Chauve. CoLoRMap: Correcting Long Reads by Mapping short reads
552 -- 558Olga V. Matveeva, Yury D. Nechipurenko, Evgeniy Riabenko, Chikako Ragan, Nafisa N. Nazipova, Aleksey Y. Ogurtsov, Svetlana A. Shabalina. Optimization of signal-to-noise ratio for efficient microarray probe design
559 -- 566Shay Ben-Elazar, Benny Chor, Zohar Yakhini. Extending partial haplotypes to full genome haplotypes using chromosome conformation capture data
567 -- 575Samuele Girotto, Cinzia Pizzi, Matteo Comin. MetaProb: accurate metagenomic reads binning based on probabilistic sequence signatures
576 -- 585Omer S. Alkhnbashi, Shiraz A. Shah, Roger A. Garrett, Sita J. Saunders, Fabrizio Costa, Rolf Backofen. Characterizing leader sequences of CRISPR loci
586 -- 594Sungyoung Lee, Sungkyoung Choi, Young-Jin Kim, Bong-Jo Kim, Heungsun Hwang, Taesung Park. Pathway-based approach using hierarchical components of collapsed rare variants
595 -- 604Kathrin Trappe, Tobias Marschall, Bernhard Y. Renard. Detecting horizontal gene transfer by mapping sequencing reads across species boundaries
605 -- 610Wenbao Yu, Seungyeoun Lee, Taesung Park. A unified model based multifactor dimensionality reduction framework for detecting gene-gene interactions
611 -- 619Jaehoon Lee, Young-Jin Kim, Juyoung Lee, Bong-Jo Kim, Seungyeoun Lee, Taesung Park. Gene-set association tests for next-generation sequencing data
620 -- 628Djordje Djordjevic, Kenro Kusumi, Joshua W. K. Ho. XGSA: A statistical method for cross-species gene set analysis
629 -- 638Tuomo Hartonen, Biswajyoti Sahu, Kashyap Dave, Teemu Kivioja, Jussi Taipale. PeakXus: comprehensive transcription factor binding site discovery from ChIP-Nexus and ChIP-Exo experiments
639 -- 648Ritambhara Singh, Jack Lanchantin, Gabriel Robins, Yanjun Qi. DeepChrome: deep-learning for predicting gene expression from histone modifications
649 -- 657I. Gregor, Alexander Schönhuth, Alice Carolyn McHardy. Snowball: strain aware gene assembly of metagenomes
658 -- 664Somaye Hashemifar, Jianzhu Ma, Hammad Naveed, Stefan Canzar, Jinbo Xu. ModuleAlign: module-based global alignment of protein-protein interaction networks
665 -- 671Konstantinos D. Tsirigos, Arne Elofsson, Pantelis G. Bagos. PRED-TMBB2: improved topology prediction and detection of beta-barrel outer membrane proteins
672 -- 679Sheng Wang, Jianzhu Ma, Jinbo Xu. AUCpreD: proteome-level protein disorder prediction by AUC-maximized deep convolutional neural fields
680 -- 684Robert Vaser, Dario Pavlovic, Mile Sikic. SWORD - a highly efficient protein database search
685 -- 692Olga S. Voitenko, Andi Dhroso, Anna Feldmann, Dmitry Korkin, Olga V. Kalinina. Patterns of amino acid conservation in human and animal immunodeficiency viruses
693 -- 701Émilie Neveu, David W. Ritchie, Petr Popov, Sergei Grudinin. PEPSI-Dock: a detailed data-driven protein-protein interaction potential accelerated by polar Fourier correlation
702 -- 709Thang V. Pham, Connie R. Jimenez. Simulated linear test applied to quantitative proteomics
710 -- 717Thach Nguyen, Michael Habeck. A probabilistic model for detecting rigid domains in protein structures
718 -- 726Bernhard Steiert, Jens Timmer, Clemens Kreutz. 1 regularization facilitates detection of cell type-specific parameters in dynamical systems
727 -- 735Hesam Montazeri, Jack Kuipers, Roger D. Kouyos, Jürg Böni, Sabine Yerly, Thomas Klimkait, Vincent Aubert, Huldrych F. Günthard, Niko Beerenwinkel, The Swiss Hiv Cohort Study. Large-scale inference of conjunctive Bayesian networks
736 -- 745Mark D. M. Leiserson, Matthew A. Reyna, Benjamin J. Raphael. A weighted exact test for mutually exclusive mutations in cancer
746 -- 754Matthew Ruffalo, Ziv Bar-Joseph. Genome wide predictions of miRNA regulation by transcription factors
755 -- 762Max Sajitz-Hermstein, Nadine Töpfer, Sabrina Kleessen, Alisdair R. Fernie, Zoran Nikoloski. iReMet-flux: constraint-based approach for integrating relative metabolite levels into a stoichiometric metabolic models
763 -- 771Hung-Cuong Trinh, Yung-Keun Kwon. Edge-based sensitivity analysis of signaling networks by using Boolean dynamics
772 -- 780Pauline Traynard, Adrien Fauré, François Fages, Denis Thieffry. Logical model specification aided by model-checking techniques: application to the mammalian cell cycle regulation
781 -- 789Konstantinos Koutroumpas, Paolo Ballarini, Irene Votsi, Paul-Henry Cournède. Bayesian parameter estimation for the Wnt pathway: an infinite mixture models approach
790 -- 797Daniel Sánchez-Taltavull, Matthew MacLeod, Theodore J. Perkins. On cross-conditional and fluctuation correlations in competitive RNA networks
2567 -- 2576Jiarui Ding, Sohrab P. Shah, Anne Condon. densityCut: an efficient and versatile topological approach for automatic clustering of biological data
2577 -- 2581Elias Dohmen, Lukas P. M. Kremer, Erich Bornberg-Bauer, Carsten Kemena. DOGMA: domain-based transcriptome and proteome quality assessment
2582 -- 2589Ivan Sovic, Kresimir Krizanovic, Karolj Skala, Mile Sikic. de novo assembly of nanopore reads
2590 -- 2597Liam Harold Childs, Soulafa Mamlouk, Jörgen Brandt, Christine Sers, Ulf Leser. SoFIA: a data integration framework for annotating high-throughput datasets
2598 -- 2603T. Bernard Bigdeli, Donghyung Lee, Bradley Todd Webb, Brien P. Riley, Vladimir I. Vladimirov, Ayman H. Fanous, Kenneth S. Kendler, Silviu-Alin Bacanu. A simple yet accurate correction for winner's curse can predict signals discovered in much larger genome scans
2604 -- 2610Raivo Kolde, Kaspar Märtens, Kaie Lokk, Sven Laur, Jaak Vilo. seqlm: an MDL based method for identifying differentially methylated regions in high density methylation array data
2611 -- 2617Eric Z. Chen, Hongzhe Li. A two-part mixed-effects model for analyzing longitudinal microbiome compositional data
2618 -- 2625Zheng-Zheng Tang, Guanhua Chen, Alexander V. Alekseyenko. PERMANOVA-S: association test for microbial community composition that accommodates confounders and multiple distances
2626 -- 2635Sudhakar Sahoo, Michal P. Switnicki, Jakob Skou Pedersen. ProbFold: a probabilistic method for integration of probing data in RNA secondary structure prediction
2636 -- 2641Ganapathi Varma Saripella, Erik L. L. Sonnhammer, Kristoffer Forslund. Benchmarking the next generation of homology inference tools
2642 -- 2649Gelio Alves, Yi-Kuo Yu. Confidence assignment for mass spectrometry based peptide identifications via the extreme value distribution
2650 -- 2658David W. Ritchie. Calculating and scoring high quality multiple flexible protein structure alignments
2659 -- 2663Liang Niu, Zongli Xu, Jack A. Taylor. RCP: a novel probe design bias correction method for Illumina Methylation BeadChip
2664 -- 2671HuiMin Luo, Jianxin Wang, Min Li, Junwei Luo, Xiaoqing Peng, Fang-Xiang Wu, Yi Pan. Drug repositioning based on comprehensive similarity measures and Bi-Random walk algorithm
2672 -- 2680Francesco Pappalardo, Epifanio Fichera, Nicoletta Paparone, Alessandro Lombardo, Marzio Pennisi, Giulia Russo, Marco Leotta, Francesco Pappalardo, Alessandro Pedretti, Francesco De Fiore, Santo Motta. A computational model to predict the immune system activation by citrus-derived vaccine adjuvants
2681 -- 2685Daniel Lobo, Junji Morokuma, Michael Levin. hnf4 as a regulatory gene in planarian regeneration
2686 -- 2691Jonathan D. Wren. Bioinformatics programs are 31-fold over-represented among the highest impact scientific papers of the past two decades
2692 -- 2695Zheng Xu, Guosheng Zhang, Cong Wu, Yun Li, Ming Hu. FastHiC: a fast and accurate algorithm to detect long-range chromosomal interactions from Hi-C data
2696 -- 2698Elena Yavorska Harris, Rachid Ounit, Stefano Lonardi. BRAT-nova: fast and accurate mapping of bisulfite-treated reads
2699 -- 2701Paul P. S. Wang, Wendy T. Parker, Susan Branford, Andreas W. Schreiber. BAM-matcher: a tool for rapid NGS sample matching
2702 -- 2703Ben J. Woodcroft, Joel A. Boyd, Gene W. Tyson. OrfM: a fast open reading frame predictor for metagenomic data
2704 -- 2706Bianca K. Stöcker, Johannes Köster, Sven Rahmann. SimLoRD: Simulation of Long Read Data
2707 -- 2709B. D. Pickett, S. M. Karlinsey, C. E. Penrod, M. J. Cormier, Mark T. W. Ebbert, Dennis K. Shiozawa, C. J. Whipple, Perry G. Ridge. SA-SSR: a suffix array-based algorithm for exhaustive and efficient SSR discovery in large genetic sequences
2710 -- 2712Marianna Sakka, Grigorios Tzortzis, Michalis D. Mantzaris, Nick Bekas, Tahsin F. Kellici, Aristidis Likas, Dimitrios Galaris, Ioannis P. Gerothanassis, Andreas G. Tzakos. PRESS: PRotEin S-Sulfenylation server
2713 -- 2715Ivan H. Goenawan, Kenneth Bryan, David J. Lynn. DyNet: visualization and analysis of dynamic molecular interaction networks
2716 -- 2718Devin K. Schweppe, Chunxiang Zheng, Juan D. Chavez, Arti T. Navare, Xia Wu, Jimmy K. Eng, James E. Bruce. XLinkDB 2.0: integrated, large-scale structural analysis of protein crosslinking data
2719 -- 2721Maciej J. Swat, Pierre Grenon, Sarala M. Wimalaratne. ProbOnto: ontology and knowledge base of probability distributions
2722 -- 2724Anna Lukasik, Maciej Wójcikowski, Piotr Zielenkiewicz. Tools4miRs - one place to gather all the tools for miRNA analysis
2725 -- 2726Julia Varga, László Dobson, Gábor E. Tusnády. TOPDOM: database of conservatively located domains and motifs in proteins
2727 -- 0Li Teng, Bing He, Jiahui Wang, Kai Tan. 4DGenome: a comprehensive database of chromatin interactions

Volume 32, Issue 16

2403 -- 2410Xu Hua, Luxiao Chen, Jin Wang, Jie Li, Edgar Wingender. Identifying cell-specific microRNA transcriptional start sites
2411 -- 2418Bin Liu 0014, Ren Long, Kuo-Chen Chou. iDHS-EL: identifying DNase I hypersensitive sites by fusing three different modes of pseudo nucleotide composition into an ensemble learning framework
2419 -- 2426Aleksander Jankowski, Jerzy Tiuryn, Shyam Prabhakar. Romulus: robust multi-state identification of transcription factor binding sites from DNase-seq data
2427 -- 2434En-Shiun Annie Lee, Fiona J. Whelan, Dawn M. E. Bowdish, Andrew K. C. Wong. Partitioning and correlating subgroup characteristics from Aligned Pattern Clusters
2435 -- 2443Jing Yang, Qi-Yu Jin, Biao Zhang, Hong-bin Shen. ab initio residue contact map prediction using dynamic fusion strategy and Gaussian noise filter
2444 -- 2450Naama Hurwitz, Dina Schneidman-Duhovny, Haim J. Wolfson. Memdock: an α-helical membrane protein docking algorithm
2451 -- 2456Daisuke Kuroda, Jeffrey J. Gray. Shape complementarity and hydrogen bond preferences in protein-protein interfaces: implications for antibody modeling and protein-protein docking
2457 -- 2463Kerstin Bunte, Eemeli Leppäaho, Inka Saarinen, Samuel Kaski. Sparse group factor analysis for biclustering of multiple data sources
2464 -- 2472Eva-Maria Geissen, Jan Hasenauer, Stephanie Heinrich, Silke Hauf, Fabian J. Theis, Nicole Radde. MEMO: multi-experiment mixture model analysis of censored data
2473 -- 2480Gianni Monaco, Hao Chen, Michael Poidinger, Jinmiao Chen, João Pedro de Magalhães, Anis Larbi. flowAI: automatic and interactive anomaly discerning tools for flow cytometry data
2481 -- 2489Venetia Pliatsika, Phillipe Loher, Aristeidis G. Telonis, Isidore Rigoutsos. MINTbase: a framework for the interactive exploration of mitochondrial and nuclear tRNA fragments
2490 -- 2498Subhadip Basu, Dariusz Plewczynski, Satadal Saha, Matylda Roszkowska, Marta Magnowska, Ewa Baczynska, Jakub Wlodarczyk. 2dSpAn: semiautomated 2-d segmentation, classification and analysis of hippocampal dendritic spine plasticity
2499 -- 2501Tarun Mall, John Eckstein, David C. Norris, Hiral Vora, Nowlan H. Freese, Ann E. Loraine. ProtAnnot: an App for Integrated Genome Browser to display how alternative splicing and transcription affect proteins
2502 -- 2504Hyungro Lee, Min Su Lee, Wazim Mohammed Ismail, Mina Rho, Geoffrey C. Fox, Sangyoon Oh, Haixu Tang. MGEScan: a Galaxy-based system for identifying retrotransposons in genomes
2505 -- 2507E. Andres Houseman, Kevin C. Johnson, Brock C. Christensen. OxyBS: estimation of 5-methylcytosine and 5-hydroxymethylcytosine from tandem-treated oxidative bisulfite and bisulfite DNA
2508 -- 2510William Chow, Kim Brugger, Mario Cáccamo, Ian Sealy, James Torrance, Kerstin Howe. gEVAL - a web-based browser for evaluating genome assemblies
2511 -- 2513E. C. Schofield, Tim Carver, Premanand Achuthan, P. Freire-Pritchett, M. Spivakov, John A. Todd, Oliver S. Burren. CHiCP: a web-based tool for the integrative and interactive visualization of promoter capture Hi-C datasets
2514 -- 2516Peng Jiang, James A. Thomson, Ron M. Stewart. Quality control of single-cell RNA-seq by SinQC
2517 -- 2519Alexander J. Titus, E. Andres Houseman, Kevin C. Johnson, Brock C. Christensen. methyLiftover: cross-platform DNA methylation data integration
2520 -- 2523Jens Roat Kultima, Luis Pedro Coelho, Kristoffer Forslund, Jaime Huerta-Cepas, Simone S. Li, Marja Driessen, Anita Yvonne Voigt, Georg Zeller, Shinichi Sunagawa, Peer Bork. MOCAT2: a metagenomic assembly, annotation and profiling framework
2524 -- 2525Miguel Pignatelli. TnT: a set of libraries for visualizing trees and track-based annotations for the web
2526 -- 2527Yousong Peng, Lei Yang, Honglei Li, Yuanqiang Zou, Lizong Deng, Aiping Wu, Xiangjun Du, Dayan Wang, Yuelong Shu, Taijiao Jiang. PREDAC-H3: a user-friendly platform for antigenic surveillance of human influenza a(H3N2) virus based on hemagglutinin sequences
2528 -- 2530Romain Fenouil, Nicolas Descostes, Lionel Spinelli, Frederic Koch, Muhammad Ahmad Maqbool, Touati Benoukraf, Pierre Cauchy, Charlène Innocenti, Pierre Ferrier, Jean-Christophe Andrau. Pasha: a versatile R package for piling chromatin HTS data
2531 -- 2533Kota Kasahara, Neetha Mohan, Ikuo Fukuda, Haruki Nakamura. mDCC_tools: characterizing multi-modal atomic motions in molecular dynamics trajectories
2534 -- 2536Hui-Chun Lu, Julián Herrera Braga, Franca Fraternali. PinSnps: structural and functional analysis of SNPs in the context of protein interaction networks
2537 -- 2538Jimmy C. F. Ngai, Pui-In Mak, Shirley W. I. Siu. ProtPOS: a python package for the prediction of protein preferred orientation on a surface
2539 -- 2541Erik Walinda, Daichi Morimoto, Mayu Nishizawa, Masahiro Shirakawa, Kenji Sugase. Amaterasu
2542 -- 2544Castrense Savojardo, Piero Fariselli, Pier Luigi Martelli, Rita Casadio. INPS-MD: a web server to predict stability of protein variants from sequence and structure
2545 -- 2547Zachary Ziegler, Molly Schmidt, Thomas Gurry, Virginia Burger, Collin M. Stultz. Mollack: a web server for the automated creation of conformational ensembles for intrinsically disordered proteins
2548 -- 2550Guillaume Postic, Yassine Ghouzam, Jean-Christophe Gelly. OREMPRO web server: orientation and assessment of atomistic and coarse-grained structures of membrane proteins
2551 -- 2553Abhinav Nellore, Christopher Wilks, Kasper D. Hansen, Jeffrey T. Leek, Ben Langmead. Rail-dbGaP: analyzing dbGaP-protected data in the cloud with Amazon Elastic MapReduce
2554 -- 2555Linda Odenthal-Hesse, Julien Y. Dutheil, Fabian Klötzl, Bernhard Haubold. hotspot: software to support sperm-typing for investigating recombination hotspots
2556 -- 2558Christine B. Peterson, M. Bogomolov, Y. Benjamini, C. Sabatti. TreeQTL: hierarchical error control for eQTL findings
2559 -- 2561Timo Lubitz, Jens Hahn, Frank T. Bergmann, Elad Noor, Edda Klipp, Wolfram Liebermeister. SBtab: a flexible table format for data exchange in systems biology
2562 -- 2564Petar Velickovic, Pietro Liò. Muxstep: an open-source C ++ multiplex HMM library for making inferences on multiple data types
2565 -- 0Marta Rosikiewicz, Marc Robinson-Rechavi. IQRray, a new method for Affymetrix microarray quality control, and the homologous organ conservation score, a new benchmark method for quality control metrics

Volume 32, Issue 15

2243 -- 2247Can Firtina, Can Alkan. On genomic repeats and reproducibility
2248 -- 2255Yusuke Matsui, Masahiro Mizuta, Satoshi Ito, Satoru Miyano, Teppei Shimamura. 3M: detection of differential distributions of methylation levels
2256 -- 2263Mikhail G. Dozmorov, Lukas R. Cara, Cory B. Giles, Jonathan D. Wren. GenomeRunner web server: regulatory similarity and differences define the functional impact of SNP sets
2264 -- 2271Tunca Dogan, Alistair MacDougall, Rabie Saidi, Diego Poggioli, Alex Bateman, Claire O'Donovan, Maria Jesus Martin. UniProt-DAAC: domain architecture alignment and classification, a new method for automatic functional annotation in UniProtKB
2272 -- 2280Vitor Piro, Martin S. Lindner, Bernhard Y. Renard. DUDes: a top-down taxonomic profiler for metagenomics
2281 -- 2288Ishita K. Khan, Daisuke Kihara. Genome-scale prediction of moonlighting proteins using diverse protein association information
2289 -- 2296Daniel Zaidman, Haim J. Wolfson. PinaColada: peptide-inhibitor ant colony ad-hoc design algorithm
2297 -- 2305Sumanta Mukherjee, Chiranjib Bhattacharyya, Nagasuma Chandra. HLaffy: estimating peptide affinities for Class-1 HLA molecules by learning position-specific pair potentials
2306 -- 2312Rudy Arthur, Jared O'Connell, Ole Schulz-Trieglaff, Anthony J. Cox. Rapid genotype refinement for whole-genome sequencing data using multi-variate normal distributions
2313 -- 2320Hao Zhu, Markus R. Owen, Yanlan Mao. The spatiotemporal order of signaling events unveils the logic of development signaling
2321 -- 2329Sabrina Hross, Jan Hasenauer. Analysis of CFSE time-series data using division-, age- and label-structured population models
2330 -- 2337Pedro Saa, Lars K. Nielsen. ll-ACHRB: a scalable algorithm for sampling the feasible solution space of metabolic networks
2338 -- 2345Zichen Wang, Neil R. Clark, Avi Ma'ayan. Drug-induced adverse events prediction with the LINCS L1000 data
2346 -- 2351Ying Yang, Xiaotao Jiang, Benli Chai, Liping Ma, Bing Li, Anni Zhang, James R. Cole, James M. Tiedje, Tong Zhang. ARGs-OAP: online analysis pipeline for antibiotic resistance genes detection from metagenomic data using an integrated structured ARG-database
2352 -- 2358Ahmed Fakhry, Hanchuan Peng, Shuiwang Ji. Deep models for brain EM image segmentation: novel insights and improved performance
2359 -- 2360Christian Arnold, Pooja Bhat, Judith B. Zaugg. SNPhood: investigate, quantify and visualise the epigenomic neighbourhood of SNPs using NGS data
2361 -- 2363Mariusz Butkiewicz, Jessica Cooke Bailey, Alex T. Frase, Scott M. Dudek, Brian L. Yaspan, Marylyn D. Ritchie, Sarah A. Pendergrass, Jonathan L. Haines. Pathway analysis by randomization incorporating structure - PARIS: an update
2364 -- 2365Joshua Millstein, Gary K. Chen, Carrie V. Breton. cit: hypothesis testing software for mediation analysis in genomic applications
2366 -- 2368Karen Y. Oróstica, Ricardo A. Verdugo. chromPlot: visualization of genomic data in chromosomal context
2369 -- 2371Yun Heo, Anand Ramachandran, Wen-mei W. Hwu, Jian Ma, Deming Chen. BLESS 2: accurate, memory-efficient and fast error correction method
2372 -- 2374Zuguang Gu, Roland Eils, Matthias Schlesner. HilbertCurve: an R/Bioconductor package for high-resolution visualization of genomic data
2375 -- 2377Eric Roller, Sergii Ivakhno, Steve Lee, Thomas Royce, Stephen Tanner. Canvas: versatile and scalable detection of copy number variants
2378 -- 2379Dan Vanderkam, Bülent Arman Aksoy, Isaac Hodes, Jaclyn Perrone, Jeff Hammerbacher. pileup.js: a JavaScript library for interactive and in-browser visualization of genomic data
2380 -- 2381Vladimir Novichkov, Anna Kaznadzey, Natalia Alexandrova, Denis Kaznadzey. NSimScan: DNA comparison tool with increased speed, sensitivity and accuracy
2382 -- 2383Yi Wang, Vijay K. Tiwari, Nidhi Rawat, Bikram S. Gill, Naxin Huo, Frank M. You, Devin Coleman-Derr, Yong Qiang Gu. GSP: a web-based platform for designing genome-specific primers in polyploids
2384 -- 2385Christian Haider, Marina Kavic, Erik L. L. Sonnhammer. TreeDom: a graphical web tool for analysing domain architecture evolution
2386 -- 2388Erney Ramirez Aportela, José Ramón López-Blanco, Pablo Chacón. FRODOCK 2.0: fast protein-protein docking server
2389 -- 2391Lyndal Henden, David Wakeham, Melanie Bahlo. XIBD: software for inferring pairwise identity by descent on the X chromosome
2392 -- 2393Nadezhda M. Belonogova, Gulnara R. Svishcheva, Tatiana I. Axenovich. FREGAT: an R package for region-based association analysis
2394 -- 2395Martin Lindén, Vladimir Curic, Alexis Boucharin, David Fange, Johan Elf. Simulated single molecule microscopy with SMeagol
2396 -- 2398Abdelrahman Hosny, Paola Vera-Licona, Reinhard C. Laubenbacher, Thibauld Favre. AlgoRun: a Docker-based packaging system for platform-agnostic implemented algorithms
2399 -- 2401Sufang Wang, Michael Gribskov, Tony R. Hazbun, Pete E. Pascuzzi. CellMiner Companion: an interactive web application to explore CellMiner NCI-60 data
2402 -- 0Yuriy Hulovatyy, Huili Chen, Tijana Milenkovic. Exploring the structure and function of temporal networks with dynamic graphlets

Volume 32, Issue 14

2083 -- 2088Yuta Narushima, Hiroko Kozuka-Hata, Kouhei Tsumoto, Jun-Ichiro Inoue, Masaaki Oyama. Quantitative phosphoproteomics-based molecular network description for high-resolution kinase-substrate interactome analysis
2089 -- 2095Nowlan H. Freese, David C. Norris, Ann E. Loraine. Integrated genome browser: visual analytics platform for genomics
2096 -- 2102Filipe G. Vieira, Anders Albrechtsen, Rasmus Nielsen. Estimating IBD tracts from low coverage NGS data
2103 -- 2110Heng Li. Minimap and miniasm: fast mapping and de novo assembly for noisy long sequences
2111 -- 2119Yann Christinat, Rafal Pawlowski, Wilhelm Krek. jSplice: a high-performance method for accurate prediction of alternative splicing events and its application to large-scale renal cancer transcriptome data
2120 -- 2127Heeju Noh, Rudiyanto Gunawan. Inferring gene targets of drugs and chemical compounds from gene expression profiles
2128 -- 2135Trung-Nghia Vu, Quin F. Wills, Krishna R. Kalari, Nifang Niu, Liewei Wang, Mattias Rantalainen, Yudi Pawitan. Beta-Poisson model for single-cell RNA-seq data analyses
2136 -- 2142André Lacour, David Ellinghaus, Stefan Schreiber, Andre Franke, Tim Becker. Haplotype synthesis analysis reveals functional variants underlying known genome-wide associated susceptibility loci
2143 -- 2150Pei Chen, Rui Liu, Yongjun Li, Luonan Chen. Detecting critical state before phase transition of complex biological systems by hidden Markov model
2151 -- 2158Jie Chen, Alfred O. Hero III, Indika Rajapakse. Spectral identification of topological domains
2159 -- 2166Vincenzo Bonnici, Federico Busato, Giovanni Micale, Nicola Bombieri, Alfredo Pulvirenti, Rosalba Giugno. APPAGATO: an APproximate PArallel and stochastic GrAph querying TOol for biological networks
2167 -- 2175Charles Blatti, Saurabh Sinha. Characterizing gene sets using discriminative random walks with restart on heterogeneous biological networks
2176 -- 2183Chao Pang, David van Enckevort, Mark de Haan, Fleur Kelpin, Jonathan Jetten, Dennis Hendriksen, Tommy de Boer, Bart Charbon, Erwin Winder, K. Joeri van der Velde, Dany Doiron, Isabel Fortier, Hans Hillege, Morris A. Swertz. MOLGENIS/connect: a system for semi-automatic integration of heterogeneous phenotype data with applications in biobanks
2184 -- 2192Ying-Ying Xu, Fan Yang, Hong-bin Shen. Incorporating organelle correlations into semi-supervised learning for protein subcellular localization prediction
2193 -- 2195Anestis Touloumis, John C. Marioni, Simon Tavaré. HDTD: analyzing multi-tissue gene expression data
2196 -- 2198Dongwon Lee. LS-GKM: a new gkm-SVM for large-scale datasets
2199 -- 2201Andreas Bremges, Esther Singer, Tanja Woyke, Alexander Sczyrba. MeCorS: Metagenome-enabled error correction of single cell sequencing reads
2202 -- 2204Birte Kehr, Páll Melsted. chopBAI: BAM index reduction solves I/O bottlenecks in the joint analysis of large sequencing cohorts
2205 -- 2207Mahmoud Ghandi, Morteza Mohammad Noori, Narges Ghareghani, Dongwon Lee, Levi A. Garraway, Michael A. Beer. gkmSVM: an R package for gapped-kmer SVM
2208 -- 2209Christopher J. R. Illingworth. SAMFIRE: multi-locus variant calling for time-resolved sequence data
2210 -- 2212Elena Bushmanova, Dmitry Antipov, Alla Lapidus, Vladimir Suvorov, Andrey D. Prjibelski. de novo transcriptome assemblies
2213 -- 2215Oz Solomon, Eran Eyal, Ninette Amariglio, Ron Unger, Gidi Rechavi. e23D: database and visualization of A-to-I RNA editing sites mapped to 3D protein structures
2216 -- 2218Hui Liu, Tingjun Hou. CaFE: a tool for binding affinity prediction using end-point free energy methods
2219 -- 2220Aaron Diaz, Siyuan J. Liu, Carmen Sandoval, Alex Pollen, Tom J. Nowakowski, Daniel A. Lim, Arnold Kriegstein. SCell: integrated analysis of single-cell RNA-seq data
2221 -- 2223Xiao Huo, Sheng'en Hu, Chengchen Zhao, Yong Zhang. Dr.seq: a quality control and analysis pipeline for droplet sequencing
2224 -- 2226Sophie Limou, Andrew M. Taverner, Cheryl A. Winkler. Ferret: a user-friendly Java tool to extract data from the 1000 Genomes Project
2227 -- 2229Qian S. Zhang, Brian L. Browning, Sharon R. Browning. ASAFE: ancestry-specific allele frequency estimation
2230 -- 2232Haiming Tang, Paul D. Thomas. PANTHER-PSEP: predicting disease-causing genetic variants using position-specific evolutionary preservation
2233 -- 2235Alexander Lachmann, Federico M. Giorgi, Gonzalo López, Andrea Califano. ARACNe-AP: gene network reverse engineering through adaptive partitioning inference of mutual information
2236 -- 2238Núria Queralt-Rosinach, Janet Piñero, Àlex Bravo, Ferran Sanz, Laura I. Furlong. DisGeNET-RDF: harnessing the innovative power of the Semantic Web to explore the genetic basis of diseases
2239 -- 2241Leonid Andronov, Yves Lutz, Jean-Luc Vonesch, Bruno P. Klaholz. SharpViSu: integrated analysis and segmentation of super-resolution microscopy data
2242 -- 0Brendan O'Fallon. TreesimJ: a flexible, forward time population genetic simulator

Volume 32, Issue 13

1921 -- 1924Volkan Sevim, Ali Bashir, Chen-Shan Chin, Karen H. Miga. Alpha-CENTAURI: assessing novel centromeric repeat sequence variation with long read sequencing
1925 -- 1932Kristoffer Sahlin, Rayan Chikhi, Lars Arvestad. Assembly scaffolding with PE-contaminated mate-pair libraries
1933 -- 1942Kazutaka Katoh, Daron M. Standley. A simple method to control over-alignment in the MAFFT multiple sequence alignment program
1943 -- 1951Yuval Elhanati, Quentin Marcou, Thierry Mora, Aleksandra M. Walczak. repgenHMM: a dynamic programming tool to infer the rules of immune receptor generation from sequence data
1952 -- 1958François D. Richard, Ronnie Alves, Andrey V. Kajava. Tally: a scoring tool for boundary determination between repetitive and non-repetitive protein sequences
1959 -- 1965Alexander Lachmann, Federico M. Giorgi, Mariano J. Alvarez, Andrea Califano. Detection and removal of spatial bias in multiwell assays
1966 -- 1973Sunghwan Kim, Chien-Wei Lin, George C. Tseng. MetaKTSP: a meta-analytic top scoring pair method for robust cross-study validation of omics prediction analysis
1974 -- 1980Kevin Sharp, Warren Kretzschmar, Olivier Delaneau, Jonathan Marchini. Phasing for medical sequencing using rare variants and large haplotype reference panels
1981 -- 1989Anna Cichonska, Juho Rousu, Pekka Marttinen, Antti J. Kangas, Pasi Soininen, Terho Lehtimäki, Olli T. Raitakari, Marjo-Riitta Järvelin, Veikko Salomaa, Mika Ala-Korpela, Samuli Ripatti, Matti Pirinen. metaCCA: summary statistics-based multivariate meta-analysis of genome-wide association studies using canonical correlation analysis
1990 -- 2000Laura Buzdugan, Markus Kalisch, Arcadi Navarro, Daniel Schunk, Ernst Fehr, Peter Bühlmann. Assessing statistical significance in multivariable genome wide association analysis
2001 -- 2007Luis Tobalina, Jon Pey, Francisco J. Planes. Direct calculation of minimal cut sets involving a specific reaction knock-out
2008 -- 2016Alexander Eng, Elhanan Borenstein. An algorithm for designing minimal microbial communities with desired metabolic capacities
2017 -- 2023Jeongbin Park, Jin-Soo Kim, Sangsu Bae. Cas-Database: web-based genome-wide guide RNA library design for gene knockout screens using CRISPR-Cas9
2024 -- 2025Kenneth A. Watanabe, Kaiwang Ma, Arielle Homayouni, Paul J. Rushton, Qingxi J. Shen. Transcript structure and domain display: a customizable transcript visualization tool
2026 -- 2028James G. Lamine, Randall J. DeJong, Serita M. Nelesen. PhamDB: a web-based application for building Phamerator databases
2029 -- 2031Jeremiah Wala, Cheng-Zhong Zhang, Matthew Meyerson, Rameen Beroukhim. VariantBam: filtering and profiling of next-generational sequencing data using region-specific rules
2032 -- 2034Yang Yang, Abhishek Niroula, Bairong Shen, Mauno Vihinen. PON-Sol: prediction of effects of amino acid substitutions on protein solubility
2035 -- 2037Susan K. Van Riper, LeeAnn Higgins, John V. Carlis, Timothy J. Griffin. RIPPER: a framework for MS1 only metabolomics and proteomics label-free relative quantification
2038 -- 2040Federico Mattiello, Bie M. P. Verbist, Karoline Faust, Jeroen Raes, William D. Shannon, Luc Bijnens, Olivier Thas. A web application for sample size and power calculation in case-control microbiome studies
2041 -- 2043Chuming Chen, Hongzhan Huang, Raja Mazumder, Darren A. Natale, Peter B. McGarvey, Jian Zhang, Shawn W. Polson, Yuqi Wang, Cathy H. Wu, UniProt Consortium. Computational clustering for viral reference proteomes
2044 -- 2046Benjamin Schubert, Mathias Walzer, Hans-Philipp Brachvogel, András Szolek, Christopher Mohr, Oliver Kohlbacher. FRED 2: an immunoinformatics framework for Python
2047 -- 2049Samuel M. Nicholls, Amanda Clare, Joshua C. Randall. Goldilocks: a tool for identifying genomic regions that are 'just right'
2050 -- 2052Baekdoo Kim, Thahmina Ali, Samuel Hosmer, Konstantinos Krampis. Visual Omics Explorer (VOE): a cross-platform portal for interactive data visualization
2053 -- 2055Alexander Ekstrom, Yanbin Yin. ORFanFinder: automated identification of taxonomically restricted orphan genes
2056 -- 2058Edwin Jacox, Cédric Chauve, Gergely J. Szöllosi, Yann Ponty, Céline Scornavacca. ecceTERA: comprehensive gene tree-species tree reconciliation using parsimony
2059 -- 2061Debswapna Bhattacharya, Badri Adhikari, Jilong Li, Jianlin Cheng. FRAGSION: ultra-fast protein fragment library generation by IOHMM sampling
2062 -- 2064Alejandro Panjkovich, Dmitri I. Svergun. SASpy: a PyMOL plugin for manipulation and refinement of hybrid models against small angle X-ray scattering data
2065 -- 2066Syed Asad Rahman, Gilliean Torrance, Lorenzo Baldacci, Sergio Martínez Cuesta, Franz Fenninger, Nimish Gopal, Saket Choudhary, John W. May, Gemma L. Holliday, Christoph Steinbeck, Janet M. Thornton. Reaction Decoder Tool (RDT): extracting features from chemical reactions
2067 -- 2068Ahmed Mohamed, Canh Hao Nguyen, Hiroshi Mamitsuka. NMRPro: an integrated web component for interactive processing and visualization of NMR spectra
2069 -- 2071Yuanwei Zhang, Qiguang Zang, Bo Xu, Wei Zheng, Rongjun Ban, Huan Zhang, Yifan Yang, QiaoMei Hao, Furhan Iqbal, Ao Li, Qinghua Shi. IsomiR Bank: a research resource for tracking IsomiRs
2072 -- 2074Karthik Gangavarapu, Vyshakh Babji, Tobias Meißner, Andrew I. Su, Benjamin M. Good. Branch: an interactive, web-based tool for testing hypotheses and developing predictive models
2075 -- 2077Laurent Gole, Kok Haur Ong, Thomas Boudier, Weimiao Yu, Sohail Ahmed. OpenSegSPIM: a user-friendly segmentation tool for SPIM data
2078 -- 0Ognjen Arandjelovic. On the discovery of hospital admission patterns - a clarification
2079 -- 2080Guillermo López-Campos, Fernando José Martín-Sánchez, Kathleen Gray. Comment on 'Discovering hospital admission patterns using models learnt from electronic hospital records'. The importance of using the right codes
2081 -- 0SungChul Kim, Lee Sael, Hwanjo Yu. k patient search exploiting Gene-Ontology and orthogonal non-negative matrix factorization

Volume 32, Issue 12

1 -- 2Pierre Baldi, Teresa M. Przytycka. ISMB 2016 Proceedings
8 -- 17Forest Agostinelli, Nicholas Ceglia, Babak Shahbaba, Paolo Sassone-Corsi, Pierre Baldi. What time is it? Deep learning approaches for circadian rhythms
18 -- 27Qingjun Yuan, Junning Gao, Dongliang Wu, Shihua Zhang, Hiroshi Mamitsuka, Shanfeng Zhu. DrugE-Rank: improving drug-target interaction prediction of new candidate drugs or targets by ensemble learning to rank
28 -- 36Céline Brouard, Huibin Shen, Kai Dührkop, Florence d'Alché-Buc, Sebastian Böcker, Juho Rousu. Fast metabolite identification with Input Output Kernel Regression
37 -- 43Dan He, David Kuhn, Laxmi Parida. Novel applications of multitask learning and multiple output regression to multiple genetic trait prediction
44 -- 51Yue Deng, Steven J. Altschuler, Lani F. Wu. PHOCOS: inferring multi-feature phenotypic crosstalk networks
52 -- 59Oren Z. Kraus, Lei Jimmy Ba, Brendan J. Frey. Classifying and segmenting microscopy images with deep multiple instance learning
60 -- 69Reza Haydarlou, Annika Jacobsen, Nicola Bonzanni, K. Anton Feenstra, Sanne Abeln, Jaap Heringa. BioASF: a framework for automatically generating executable pathway models specified in BioPAX
70 -- 79Shengwen Peng, Ronghui You, Hongning Wang, ChengXiang Zhai, Hiroshi Mamitsuka, Shanfeng Zhu. DeepMeSH: deep semantic representation for improving large-scale MeSH indexing
80 -- 89A. Grant Schissler, Qike Li, James L. Chen, Colleen Kenost, Ikbel Achour, Dean Billheimer, Haiquan Li, Walter W. Piegorsch, Yves A. Lussier. Analysis of aggregated cell-cell statistical distances within pathways unveils therapeutic-resistance mechanisms in circulating tumor cells
90 -- 100Marinka Zitnik, Blaz Zupan. Jumping across biomedical contexts using compressive data fusion
101 -- 110Benjamin S. Glicksberg, Li Li, Marcus A. Badgeley, Khader Shameer, Roman Kosoy, Noam D. Beckmann, Nam Pho, Jörg Hakenberg, Meng Ma, Kristin L. Ayers, Gabriel E. Hoffman, Shuyu Dan Li, Eric E. Schadt, Chirag J. Patel, Rong Chen, Joel T. Dudley. Comparative analyses of population-scale phenomic data in electronic medical records reveal race-specific disease networks
111 -- 120Xihao Hu, Christina Huan Shi, Kevin Y. Yip. A novel method for discovering local spatial clusters of genomic regions with functional relationships from DNA contact maps
121 -- 127Haoyang Zeng, Matthew D. Edwards, Ge Liu, David K. Gifford. Convolutional neural network architectures for predicting DNA-protein binding
128 -- 136Kyuri Jo, Inuk Jung, Ji Hwan Moon, Sun Kim. Influence maximization in time bounded network identifies transcription factors regulating perturbed pathways
137 -- 146Jiangwen Sun, Zongliang Jiang, Xiuchun Tian, Jinbo Bi. A cross-species bi-clustering approach to identifying conserved co-regulated genes
147 -- 155Hande Topa, Antti Honkela. Analysis of differential splicing suggests different modes of short-term splicing regulation
156 -- 163Dat Duong, Jennifer Zou, Farhad Hormozdiari, Jae Hoon Sul, Jason Ernst, Buhm Han, Eleazar Eskin. Using genomic annotations increases statistical power to detect eGenes
164 -- 173Seunghak Lee, Soonho Kong, Eric P. Xing. A network-driven approach for genome-wide association mapping
174 -- 182Bo Liu, Dixian Zhu, Yadong Wang. deBWT: parallel construction of Burrows-Wheeler Transform for large collection of genomes with de Bruijn-branch encoding
183 -- 191Tzu-Yu Liu, Yun S. Song. Prediction of ribosome footprint profile shapes from transcript sequences
192 -- 200Avi Srivastava, Hirak Sarkar, Nitish Gupta, Robert Patro. RapMap: a rapid, sensitive and accurate tool for mapping RNA-seq reads to transcriptomes
201 -- 208Rayan Chikhi, Antoine Limasset, Paul Medvedev. Compacting de Bruijn graphs from sequencing data quickly and in low memory
209 -- 215Carly E. Schaeffer, Nathaniel D. Figueroa, Xiaolin Liu, John E. Karro. phRAIDER: Pattern-Hunter based Rapid Ab Initio Detection of Elementary Repeats
216 -- 224Volodymyr Kuleshov, Michael P. Snyder, Serafim Batzoglou. Genome assembly from synthetic long read clouds
225 -- 233Yufeng Wu. An algorithm for computing the gene tree probability under the multispecies coalescent and its application in the inference of population tree
234 -- 242Shilpa Garg, Marcel Martin, Tobias Marschall. Read-based phasing of related individuals
243 -- 252Shahin Mohammadi, Ananth Grama. A convex optimization approach for identification of human tissue-specific interactomes
253 -- 261Siddhartha Jain, Joel Arrais, Narasimhan J. Venkatachari, Velpandi Ayyavoo, Ziv Bar-Joseph. Reconstructing the temporal progression of HIV-1 immune response pathways
262 -- 270Sankar Basu, Björn Wallner. Finding correct protein-protein docking models using ProQDock
271 -- 277Arnon Mazza, Konrad Klockmeier, Erich E. Wanker, Roded Sharan. An integer programming framework for inferring disease complexes from network data
278 -- 287Yasuo Tabei, Yoshihiro Yamanishi, Masaaki Kotera. de novo metabolic pathway reconstruction
288 -- 296Jukka Intosalmi, Kari Nousiainen, Helena Ahlfors, Harri Lähdesmäki. Data-driven mechanistic analysis method to reveal dynamically evolving regulatory networks
297 -- 305Ewa Szczurek, Niko Beerenwinkel. Linear effects models of signaling pathways from combinatorial perturbation data
306 -- 313Alvin Farrel, Jonathan Murphy, Jun-tao Guo. Structure-based prediction of transcription factor binding specificity using an integrative energy function
314 -- 321Michal Jamróz, Andrzej Kolinski, Daisuke Kihara. Ensemble-based evaluation for protein structure models
322 -- 331Shengjie Wang, John Halloran, Jeff A. Bilmes, William S. Noble. Faster and more accurate graphical model identification of tandem mass spectra using trellises
332 -- 340Xuefeng Cui, Zhiwu Lu, Sheng Wang, Jim Jing-Yan Wang, Xin Gao. CMsearch: simultaneous exploration of protein sequence space and structure space improves not only protein homology detection but also protein structure prediction
341 -- 350Fanchi Meng, Lukasz A. Kurgan. DFLpred: High-throughput prediction of disordered flexible linker regions in protein sequences
351 -- 359Yaron Orenstein, Yuhao Wang, Bonnie Berger. RCK: accurate and efficient inference of sequence- and structure-based protein-RNA binding models from RNAcompete data
360 -- 368Juan Antonio Garcia-Martin, Iván Dotú, Javier Fernandez-Chamorro, Gloria Lozano, Jorge Ramajo, Encarnacion Martinez-Salas, Peter Clote. RNAiFold2T: Constraint Programming design of thermo-IRES switches
369 -- 377Mariko Tsuchiya, Kojiro Amano, Masaya Abe, Misato Seki, Sumitaka Hase, Kengo Sato, Yasubumi Sakakibara. SHARAKU: an algorithm for aligning and clustering read mapping profiles of deep sequencing in non-coding RNA processing
378 -- 385Xiaodong Cui, Jia Meng, ShaoWu Zhang, Yidong Chen, Yufei Huang. 6A peaks by modeling biological variances in MeRIP-seq data
1761 -- 1765Monica Chagoyen, Florencio Pazos. Characterization of clinical signs in the human interactome
1766 -- 1772Yingying Wei, Hao Wu. Measuring the spatial correlations of protein binding sites
1773 -- 1778Shicai Fan, Chengzhe Li, Rizi Ai, Mengchi Wang, Gary S. Firestein, Wei Wang. Computationally expanding infinium HumanMethylation450 BeadChip array data to reveal distinct DNA methylation patterns of rheumatoid arthritis
1779 -- 1787Magali Jaillard, Maud Tournoud, Faustine Meynier, Jean-Baptiste Veyrieras. Optimization of alignment-based methods for taxonomic binning of metagenomics reads
1788 -- 1796Zhen Zhang, Jianxin Wang, Junwei Luo, Xiaojun Ding, Jiancheng Zhong, Jun Wang, Fang-Xiang Wu, Yi Pan. Sprites: detection of deletions from sequencing data by re-aligning split reads
1797 -- 1804Daniele Raimondi, Andrea M. Gazzo, Marianne Rooman, Tom Lenaerts, Wim F. Vranken. Multilevel biological characterization of exomic variants at the protein level significantly improves the identification of their deleterious effects
1805 -- 1813Juan P. Bustamante, María E. Szretter, Mariela Sued, Marcelo A. Marti, Dario A. Estrin, Leonardo Boechi. A quantitative model for oxygen uptake and release in a family of hemeproteins
1814 -- 1822Victor L. Jong, Putri W. Novianti, Kit C. B. Roes, Marinus J. C. Eijkemans. Selecting a classification function for class prediction with gene expression data
1823 -- 1831Jie Zhang, Zhi Wei. An empirical Bayes change-point model for identifying 3′ and 5′ alternative splicing by next-generation RNA sequencing
1832 -- 1839Yifei Chen, Yi Li, Rajiv Narayan, Aravind Subramanian, Xiaohui Xie. Gene expression inference with deep learning
1840 -- 1847André Kahles, Cheng Soon Ong, Yi Zhong, Gunnar Rätsch. SplAdder: identification, quantification and testing of alternative splicing events from RNA-Seq data
1848 -- 1855Pei-Yuan Sung, Yi-ting Wang, Ya-Wen Yu, Ren Hua Chung. An efficient gene-gene interaction test for genome-wide association studies in trio families
1856 -- 1864Jin Liu, Xiang Wan, Shuangge Ma, Can Yang. EPS: an empirical Bayes approach to integrating pleiotropy and tissue-specific information for prioritizing risk genes
1865 -- 1872Shobhit Jain, Gary D. Bader. Predicting physiologically relevant SH3 domain mediated protein-protein interactions in yeast
1873 -- 1879Justin Wagner, Joseph N. Paulson, Xiao Wang, Bobby Bhattacharjee, Héctor Corrada Bravo. Privacy-preserving microbiome analysis using secure computation
1880 -- 1882Hao Wang, Joel McManus, Carl Kingsford. Isoform-level ribosome occupancy estimation guided by transcript abundance with Ribomap
1883 -- 1884Alastair P. Droop. fqtools: an efficient software suite for modern FASTQ file manipulation
1885 -- 1887José Augusto Salim, Luiz C. Borro, Ivan Mazoni, Inácio Yano, José G. Jardine, Goran Neshich. Multiple structure single parameter: analysis of a single protein nano environment descriptor characterizing a shared loci on structurally aligned proteins
1888 -- 1890Sabine C. Mueller, Christina Backes, Alexander Greß, Nina Baumgarten, Olga V. Kalinina, Andreas Moll, Oliver Kohlbacher, Eckart Meese, Andreas Keller. BALL-SNPgp - from genetic variants toward computational diagnostics
1891 -- 1894Florian Schmid, Matthias Schmid, Christoph Müssel, J. Eric Sträng, Christian Buske, Lars Bullinger, Johann M. Kraus, Hans A. Kestler. GiANT: gene set uncertainty in enrichment analysis
1895 -- 1897Michael DeGiorgio, Christian D. Huber, Melissa J. Hubisz, Ines Hellmann, Rasmus Nielsen. SweepFinder2: increased sensitivity, robustness and flexibility
1898 -- 1900Luke Jostins, Gilean McVean. Trinculo: Bayesian and frequentist multinomial logistic regression for genome-wide association studies of multi-category phenotypes
1901 -- 1902Andrey Ziyatdinov, Helena Brunel, Angel Martinez-Perez, Alfonso Buil, Alexandre Perera, José Manuel Soria. solarius: an R interface to SOLAR for variance component analysis in pedigrees
1903 -- 1904Paul R. Staab, Dirk Metzler. Coala: an R framework for coalescent simulation
1905 -- 1906Harold F. Gómez, Michael Hucka, Sarah M. Keating, German Nudelman, Dagmar Iber, Stuart C. Sealfon. MOCCASIN: converting MATLAB ODE models to SBML
1907 -- 1910Chih-Hsuan Wei, Robert Leaman, Zhiyong Lu. Beyond accuracy: creating interoperable and scalable text-mining web services
1911 -- 1913Luca De Sano, Giulio Caravagna, Daniele Ramazzotti, Alex Graudenzi, Giancarlo Mauri, Bud Mishra, Marco Antoniotti. TRONCO: an R package for the inference of cancer progression models from heterogeneous genomic data
1914 -- 1916Pengbo Wen, Peng Xiao, Junfeng Xia. dbDSM: a manually curated database for deleterious synonymous mutations
1917 -- 1919Jonathan W. Armond, Elina Vladimirou, Andrew D. McAinsh, Nigel J. Burroughs. KiT: a MATLAB package for kinetochore tracking

Volume 32, Issue 11

1601 -- 1609Caleb Weinreb, Benjamin J. Raphael. Identification of hierarchical chromatin domains
1610 -- 1617Yuri Pirola, Simone Zaccaria, Riccardo Dondi, Gunnar W. Klau, Nadia Pisanti, Paola Bonizzoni. HapCol: accurate and memory-efficient haplotype assembly from long reads
1618 -- 1624Faezeh Dorri, Lee Mendelowitz, Héctor Corrada Bravo. methylFlow: cell-specific methylation pattern reconstruction from high-throughput bisulfite-converted DNA sequencing
1625 -- 1631Bo Liu, Dengfeng Guan, Mingxiang Teng, Yadong Wang. rHAT: fast alignment of noisy long reads with regional hashing
1632 -- 1642Hongyi Xin, Sunny Nahar, Richard Zhu, John Emmons, Gennady Pekhimenko, Carl Kingsford, Can Alkan, Onur Mutlu. Optimal seed solver: optimizing seed selection in read mapping
1643 -- 1651SunHo Park, Seung-Jun Kim, Donghyeon Yu, Samuel Peña-Llopis, Jianjiong Gao, Jinsuk Park, Beibei Chen, Jessie Norris, Xinlei Wang, Min Chen, Min-Su Kim, Jeongsik Yong, Zabi Wardak, Kevin Choe, Michael Story, Timothy K. Starr, Jae-Ho Cheong, TaeHyun Hwang. An integrative somatic mutation analysis to identify pathways linked with survival outcomes across 19 cancer types
1652 -- 1661Kana Shimizu, Koji Nuida, Gunnar Rätsch. Efficient privacy-preserving string search and an application in genomics
1662 -- 1669Aryan Arbabi, Ladislav Rampásek, Michael Brudno. Cell-free DNA fragment-size distribution analysis for non-invasive prenatal CNV prediction
1670 -- 1677Dilip A. Durai, Marcel H. Schulz. de novo transcriptome assembly
1678 -- 1685Ali May, Bernd W. Brandt, Mohammed El-Kebir, Gunnar W. Klau, Egija Zaura, Wim Crielaard, Jaap Heringa, Sanne Abeln. metaModules identifies key functional subnetworks in microbiome-related disease
1686 -- 1696Lin Huang, Bo Wang, Ruitang Chen, Sivan Bercovici, Serafim Batzoglou. Reveel: large-scale population genotyping using low-coverage sequencing data
1697 -- 1700Anna Hakobyan, Lilit Nersisyan, Arsen Arakelyan. Quantitative trait association study for mean telomere length in the South Asian genomes
1701 -- 1708Fangfang Liu, Chong Wang, Zuowei Wu, Qijing Zhang, Peng Liu. A zero-inflated Poisson model for insertion tolerance analysis of genes based on Tn-seq data
1709 -- 1715Seungpyo Hong, Dongsup Kim. Library of binding protein scaffolds (LibBP): a computational platform for selection of binding protein scaffolds
1716 -- 1723Vered Madar, Sandra Batista. FastLSU: a more practical approach for the Benjamini-Hochberg FDR controlling procedure for huge-scale testing problems
1724 -- 1732Jinyu Chen, Shihua Zhang. Integrative analysis for identifying joint modular patterns of gene-expression and drug-response data
1733 -- 1739Mattia Zampieri, Uwe Sauer. Model-based media selection to minimize the cost of metabolic cooperation in microbial ecosystems
1740 -- 1742Ya Cui, Xiaowei Chen, Huaxia Luo, Zhen Fan, Jianjun Luo, Shunmin He, Haiyan Yue, Peng Zhang, Runsheng Chen. BioCircos.js: an interactive Circos JavaScript library for biological data visualization on web applications
1743 -- 1745Claus Børnich, Ivar Grytten, Eivind Hovig, Jonas Paulsen, Martin Cech, Geir Kjetil Sandve. Galaxy Portal: interacting with the galaxy platform through mobile devices
1746 -- 1748Bart Mesuere, Toon Willems, Felix Van der Jeugt, Bart Devreese, Peter Vandamme, Peter Dawyndt. Unipept web services for metaproteomics analysis
1749 -- 1751Vagheesh Narasimhan, Petr Danecek, Aylwyn Scally, Yali Xue, Chris Tyler-Smith, Richard Durbin. BCFtools/RoH: a hidden Markov model approach for detecting autozygosity from next-generation sequencing data
1752 -- 1754Zhihong Liu, Peng Ding, Xin Yan, Minghao Zheng, Huihao Zhou, Yuehua Xu, Yunfei Du, Qiong Gu, Jun Xu. ASDB: a resource for probing protein functions with small molecules
1755 -- 1757Javier Otegui, Robert P. Guralnick. The geospatial data quality REST API for primary biodiversity data
1758 -- 1759Christiana N. Fogg, Diane E. Kovats. Message from the ISCB: 2016 ISCB Accomplishment by a Senior Scientist Award Given to Søren Brunak
1760 -- 0Christiana N. Fogg, Diane E. Kovats. Message from the ISCB: 2016 Outstanding Contributions to ISCB Award: Burkhard Rost

Volume 32, Issue 10

1441 -- 1445Luis Sánchez-Pulido, Chris P. Ponting. Vasohibins: new transglutaminase-like cysteine proteases possessing a non-canonical Cys-His-Ser catalytic triad
1446 -- 1453Yongseok Park, Hao Wu. Differential methylation analysis for BS-seq data under general experimental design
1454 -- 1461Christian D. Schenkelberg, Christopher Bystroff. Protein backbone ensemble generation explores the local structural space of unseen natural homologs
1462 -- 1470B. Viart, C. Dias-Lopes, E. Kozlova, C. F. B. Oliveira, C. Nguyen, G. Neshich, C. Chávez-Olórtegui, F. Molina, L. F. Felicori. EPI-peptide designer: a tool for designing peptide ligand libraries based on epitope-paratope interactions
1471 -- 1478Sanjay Agravat, Xuezheng Song, Teerapat Rojsajjakul, Richard D. Cummings, David F. Smith. Computational approaches to define a human milk metaglycome
1479 -- 1485Halit Ongen, Alfonso Buil, Andrew Anand Brown, Emmanouil T. Dermitzakis, Olivier Delaneau. Fast and efficient QTL mapper for thousands of molecular phenotypes
1486 -- 1492Gabriel H. Murillo, Na You, Xiaoquan Su, Wei Cui, Muredach P. Reilly, Mingyao Li, Kang Ning, Xinping Cui. MultiGeMS: detection of SNVs from multiple samples using model selection on high-throughput sequencing data
1493 -- 1501Christian Benner, Chris C. A. Spencer, Aki S. Havulinna, Veikko Salomaa, Samuli Ripatti, Matti Pirinen. FINEMAP: efficient variable selection using summary data from genome-wide association studies
1502 -- 1508Daniel Stöckel, Tim Kehl, Patrick Trampert, Lara Schneider, Christina Backes, Nicole Ludwig, Andreas Gerasch, Michael Kaufmann 0001, Manfred Gessler, Norbert Graf, Eckart Meese, Andreas Keller, Hans-Peter Lenhof. Multi-omics enrichment analysis using the GeneTrail2 web service
1509 -- 1517Zhen Niu, Deborah Chasman, Amie J. Eisfeld, Yoshihiro Kawaoka, Sushmita Roy. Multi-task consensus clustering of genome-wide transcriptomes from related biological conditions
1518 -- 1526Muaaz Gul Awan, Fahad Saeed. MS-REDUCE: an ultrafast technique for reduction of big mass spectrometry data for high-throughput processing
1527 -- 1535Martin Strazar, Marinka Zitnik, Blaz Zupan, Jernej Ule, Tomaz Curk. Orthogonal matrix factorization enables integrative analysis of multiple RNA binding proteins
1536 -- 1543Raymond G. Cavalcante, Snehal Patil, Terry E. Weymouth, Kestutis G. Bendinskas, Alla Karnovsky, Maureen A. Sartor. ConceptMetab: exploring relationships among metabolite sets to identify links among biomedical concepts
1544 -- 1551Lei Du, Heng Huang, Jingwen Yan, Sungeun Kim, Shannon L. Risacher, Mark Inlow, Jason H. Moore, Andrew J. Saykin, Li Shen. Structured sparse canonical correlation analysis for brain imaging genetics: an improved GraphNet method
1552 -- 1554Ahmad Vaez, Peter J. van der Most, Bram P. Prins, Harold Snieder, Edwin R. van den Heuvel, Behrooz Z. Alizadeh, Ilja M. Nolte. lodGWAS: a software package for genome-wide association analysis of biomarkers with a limit of detection
1555 -- 1556Ge Tan, Boris Lenhard. TFBSTools: an R/bioconductor package for transcription factor binding site analysis
1557 -- 1558Karl W. Kroll, Ann-Katherin Eisfeld, Gerard Lozanski, Clara D. Bloomfield, John C. Byrd, James S. Blachly. MuCor: mutation aggregation and correlation
1559 -- 1561Monica-Andreea Dragan, Ismail Moghul, Anurag Priyam, Claudio Bustos, Yannick Wurm. GeneValidator: identify problems with protein-coding gene predictions
1562 -- 1564Jorge González-Domínguez, Bertil Schmidt. ParDRe: faster parallel duplicated reads removal tool for sequencing studies
1565 -- 1567Erik S. Wright, Kalin H. Vetsigian. DesignSignatures: a tool for designing primers that yields amplicons with distinct signatures
1568 -- 1570Matías R. Machado, Sergio Pantano. SIRAH tools: mapping, backmapping and visualization of coarse-grained models
1571 -- 1573Sikander Hayat, Christoph Peters, Nanjiang Shu, Konstantinos D. Tsirigos, Arne Elofsson. Inclusion of dyad-repeat pattern improves topology prediction of transmembrane β-barrel proteins
1574 -- 1576Shuai Li, Qiancheng Shen, Minyi Su, Xinyi Liu, Shaoyong Lu, Zhongjie Chen, Renxiao Wang, Jian Zhang. Alloscore: a method for predicting allosteric ligand-protein interactions
1577 -- 1579Michael Turewicz, Maike Ahrens, Caroline May, Katrin Marcus, Martin Eisenacher. PAA: an R/bioconductor package for biomarker discovery with protein microarrays
1580 -- 1582Kelly M. Burkett, Brad McNeney, Jinko Graham. Sampletrees and Rsampletrees: sampling gene genealogies conditional on SNP genotype data
1583 -- 1585Johannes Rainer, Daniel Taliun, Yuri D'Elia, Cristian Pattaro, Francisco S. Domingues, Christian X. Weichenberger. FamAgg: an R package to evaluate familial aggregation of traits in large pedigrees
1586 -- 1588Frank T. Bergmann, Sven Sahle, Christoph Zimmer. Piecewise parameter estimation for stochastic models in COPASI
1589 -- 1591Daniel K. Witvliet, Alexey Strokach, Andrés Felipe Giraldo-Forero, Joan Teyra, Recep Colak, Philip M. Kim. ELASPIC web-server: proteome-wide structure-based prediction of mutation effects on protein stability and binding affinity
1592 -- 1594Magnus D. Vigeland, Kristina S. Gjøtterud, Kaja K. Selmer. FILTUS: a desktop GUI for fast and efficient detection of disease-causing variants, including a novel autozygosity detector
1595 -- 1597Yining Liu, Min Zhao. lnCaNet: pan-cancer co-expression network for human lncRNA and cancer genes
1598 -- 1600Michael J. Meyer, Philip Geske, Haiyuan Yu. BISQUE: locus- and variant-specific conversion of genomic, transcriptomic and proteomic database identifiers

Volume 32, Issue 1

1 -- 8Zi Yang, George Michailidis. A non-negative matrix factorization method for detecting modules in heterogeneous omics multi-modal data
9 -- 16Adam Krejci, Ted R. Hupp, Matej Lexa, Borivoj Vojtesek, Petr Müller. Hammock: a hidden Markov model-based peptide clustering algorithm to identify protein-interaction consensus motifs in large datasets
17 -- 24Paul M. Bodily, M. Stanley Fujimoto, Quinn Snell, Dan Ventura, Mark J. Clement. ScaffoldScaffolder: solving contig orientation via bidirected to directed graph reduction
25 -- 34Maciej Dziubinski, Pawel Daniluk, Bogdan Lesyng. ResiCon: a method for the identification of dynamic domains, hinges and interfacial regions in proteins
35 -- 42Benoît Liquet, Pierre Lafaye De Micheaux, Boris P. Hejblum, Rodolphe Thiébaut. Group and sparse group partial least square approaches applied in genomics context
43 -- 49Brendan A. Veeneman, Sudhanshu Shukla, Saravana M. Dhanasekaran, Arul M. Chinnaiyan, Alexey I. Nesvizhskii. Two-pass alignment improves novel splice junction quantification
50 -- 57Kevin He, Yanming Li, Ji Zhu, Hongliang Liu, Jeffrey E. Lee, Christopher I. Amos, Terry Hyslop, Jiashun Jin, Huazhen Lin, Qinyi Wei, Yi Li. Component-wise gradient boosting and false discovery control in survival analysis with high-dimensional covariates
58 -- 66Paulo C. Rodrigues, Andreia Monteiro, Vanda M. Lourenço. A robust AMMI model for the analysis of genotype-by-environment data
67 -- 76Qiaozi Gao, Elisabeth Ostendorf, Jeffrey A. Cruz, Rong Jin, David M. Kramer 0001, Jin Chen. Inter-functional analysis of high-throughput phenotype data by non-parametric clustering and its application to photosynthesis
77 -- 84Begüm Genc, Ugur Dogrusoz. An algorithm for automated layout of process description maps drawn in SBGN
85 -- 95Isidro Cortes-Ciriano, Gerard J. P. van Westen, Guillaume Bouvier, Michael Nilges, John P. Overington, Andreas Bender, Thérèse E. Malliavin. Improved large-scale prediction of growth inhibition patterns using the NCI60 cancer cell line panel
96 -- 105Eunjee Lee, Koichi Ito, Yong Zhao, Eric E. Schadt, Hanna Y. Irie, Jun Zhu. Inferred miRNA activity identifies miRNA-mediated regulatory networks underlying multiple cancers
106 -- 113Emily K. Mallory, Ce Zhang, Christopher Ré, Russ B. Altman. Large-scale extraction of gene interactions from full-text literature using DeepDive
114 -- 121Wei Shao, Mingxia Liu, Daoqiang Zhang. Human cell structure-driven model construction for predicting protein subcellular location from biological images
122 -- 129Hendrik Schäfer, Tim Schäfer, Jörg Ackermann, Norbert Dichter, Claudia Döring, Sylvia Hartmann, Martin-Leo Hansmann, Ina Koch. CD30 cell graphs of Hodgkin lymphoma are not scale-free - an image analysis approach
130 -- 132Utkarsh J. Dang, Geoffrey Brian Golding. markophylo: Markov chain analysis on phylogenetic trees
133 -- 135Jonathan S. Packer, Evan K. Maxwell, Colm O'Dushlaine, Alexander E. Lopez, Frederick E. Dewey, Rostislav Chernomorsky, Aris Baras, John D. Overton, Lukas Habegger, Jeffrey G. Reid. CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing data
136 -- 139Karel Brinda, Valentina Boeva, Gregory Kucherov. RNF: a general framework to evaluate NGS read mappers
140 -- 141Arna Óskarsdóttir, Gísli Másson, Páll Melsted. BamHash: a checksum program for verifying the integrity of sequence data
142 -- 144Richard M. Leggett, Darren Heavens, Mario Caccamo, Matthew D. Clark, Robert P. Davey. NanoOK: multi-reference alignment analysis of nanopore sequencing data, quality and error profiles
145 -- 147Ronny Lorenz, Dominik Luntzer, Ivo L. Hofacker, Peter F. Stadler, Michael T. Wolfinger. SHAPE directed RNA folding
148 -- 150Diego A. Hartasánchez, Marina Brasó-Vives, Juanma Fuentes-Díaz, Oriol Vallès-Codina, Arcadi Navarro. SeDuS: segmental duplication simulator
151 -- 153Wei-Yi Cheng, Jörg Hakenberg, Shuyu Dan Li, Rong Chen. DIVAS: a centralized genetic variant repository representing 150 000 individuals from multiple disease cohorts
154 -- 156Christian Jungreuthmayer, Stefan Neubauer, Teresa Mairinger, Jürgen Zanghellini, Stephan Hann. ICT: isotope correction toolbox
157 -- 158Noah Fahlgren, Steven T. Hill, James C. Carrington, Alberto Carbonell. trans-acting small interfering RNA design
159 -- 160William Gilpin. PyPDB: a Python API for the Protein Data Bank