Journal: Bioinformatics

Volume 29, Issue 9

1105 -- 1111Seonjoo Lee, Pauline E. Chugh, Haipeng Shen, R. Eberle, Dirk P. Dittmer. Poisson factor models with applications to non-normalized microRNA profiling
1112 -- 1119Carsten Kemena, Giovanni Bussotti, Emidio Capriotti, Marc A. Martí-Renom, Cédric Notredame. Using tertiary structure for the computation of highly accurate multiple RNA alignments with the SARA-Coffee package
1120 -- 1126Catherine Mooney, Niall J. Haslam, Thérèse A. Holton, Gianluca Pollastri, Denis C. Shields. PeptideLocator: prediction of bioactive peptides in protein sequences
1127 -- 1133Zhiqiang Yan, Liyong Guo, Liang Hu, Jin Wang. Specificity and affinity quantification of protein-protein interactions
1134 -- 1140Robert Schneider, Florian Odronitz, Björn Hammesfahr, Marcel Hellkamp, Martin Kollmar. Peakr: simulating solid-state NMR spectra of proteins
1141 -- 1148Moritz Aschoff, Agnes Hotz-Wagenblatt, Karl-Heinz Glatting, Matthias Fischer, Roland Eils, Rainer König. SplicingCompass: differential splicing detection using RNA-Seq data
1149 -- 1157Thierry Rème, Dirk Hose, Charles Theillet, Bernard Klein. Modeling risk stratification in human cancer
1158 -- 1165Dafyd J. Jenkins, Bärbel Finkenstädt, David A. Rand. A temporal switch model for estimating transcriptional activity in gene expression
1166 -- 1173Giuseppe Facchetti, Giovanni Iacono, Giovanna De Palo, Claudio Altafini. A rate-distortion theory for gene regulatory networks and its application to logic gate consistency
1174 -- 1181Chia-Chin Wu, Kalpana Kannan, Steven Lin, Laising Yen, Aleksandar Milosavljevic. Identification of cancer fusion drivers using network fusion centrality
1182 -- 1189George Wu, Jason T. Yustein, Matthew N. McCall, Michael J. Zilliox, Rafael A. Irizarry, Karen Zeller, Chi V. Dang, Hongkai Ji. ChIP-PED enhances the analysis of ChIP-seq and ChIP-chip data
1190 -- 1198Noah Youngs, Duncan Penfold-Brown, Kevin Drew, Dennis Shasha, Richard Bonneau. Parametric Bayesian priors and better choice of negative examples improve protein function prediction
1199 -- 1205Misook Ha, Soondo Hong, Wen-Hsiung Li. Predicting the probability of H3K4me3 occupation at a base pair from the genome sequence context
1206 -- 1207Yoli Shavit, Pietro Liò. CytoHiC: a cytoscape plugin for visual comparison of Hi-C networks
1208 -- 1209Gabriel Renaud, Martin Kircher, Udo Stenzel, Janet Kelso. freeIbis: an efficient basecaller with calibrated quality scores for Illumina sequencers
1210 -- 1211Yan Guo, Jiang Li, Chung-I. Li, Yu Shyr, David C. Samuels. MitoSeek: extracting mitochondria information and performing high-throughput mitochondria sequencing analysis
1212 -- 1214David Weisman, Michie Yasuda, Jennifer L. Bowen. FunFrame: functional gene ecological analysis pipeline
1215 -- 1217Thierry Schüpbach, Marco Pagni, Alan Bridge, Lydie Bougueleret, Ioannis Xenarios, Lorenzo Cerutti. pfsearchV3: a code acceleration and heuristic to search PROSITE profiles
1218 -- 1219Laurie E. Grove, David R. Hall, Dmitri Beglov, Sandor Vajda, Dima Kozakov. FTFlex: accounting for binding site flexibility to improve fragment-based identification of druggable hot spots
1220 -- 1222Quan Long, Qingrun Zhang, Bjarni J. Vilhjalmsson, Petar Forai, Ümit Seren, Magnus Nordborg. JAWAMix5: an out-of-core HDF5-based java implementation of whole-genome association studies using mixed models
1223 -- 1225Xiaoyi Cao, Sheng Zhong. Enabling interspecies epigenomic comparison with CEpBrowser
1226 -- 1228Karsten Hiller, André Wegner, Daniel Weindl, Thekla Cordes, Christian M. Metallo, Joanne K. Kelleher, Gregory Stephanopoulos. NTFD - a stand-alone application for the non-targeted detection of stable isotope-labeled compounds in GC/MS data
1229 -- 1230Fengkai Zhang, Bastian Robert Angermann, Martin Meier-Schellersheim. The Simmune Modeler visual interface for creating signaling networks based on bi-molecular interactions
1231 -- 1232Olivier Taboureau, Ulrik Plesner Jacobsen, Christian Kalhauge, Daniel Edsgärd, Olga Rigina, Ramneek Gupta, Karine Audouze. HExpoChem: a systems biology resource to explore human exposure to chemicals
1233 -- 1234Jelle Scholtalbers, Jasmin Rößler, Patrick Sorn, Jos de Graaf, Valesca Boisguérin, John C. Castle, Ugur Sahin. Galaxy LIMS for next-generation sequencing
1235 -- 1237Fábio C. P. Navarro, Pedro A. F. Galante. RCPedia: a database of retrocopied genes
1238 -- 1239Samuel Croset, John P. Overington, Dietrich Rebholz-Schuhmann. Brain: biomedical knowledge manipulation

Volume 29, Issue 8

965 -- 972Anish Man Singh Shrestha, Martin C. Frith. An approximate Bayesian approach for mapping paired-end DNA reads to a reference genome
973 -- 980Heiner Klingenberg, Kathrin Petra Aßhauer, Thomas Lingner, Peter Meinicke. Protein signature-based estimation of metagenomic abundances including all domains of life and viruses
981 -- 988Valentina Indio, Pier Luigi Martelli, Castrense Savojardo, Piero Fariselli, Rita Casadio. The prediction of organelle-targeting peptides in eukaryotic proteins with Grammatical-Restrained Hidden Conditional Random Fields
989 -- 995Fabian Sievers, David Dineen, Andreas Wilm, Desmond G. Higgins. Making automated multiple alignments of very large numbers of protein sequences
996 -- 1003Maryam Abbasi, Luís Paquete, Arnaud Liefooghe, Miguel Pinheiro, Pedro Matias. Improvements on bicriteria pairwise sequence alignment: algorithms and applications
1004 -- 1010Hsueh-Ting Chu, William W. L. Hsiao, Jen-Chih Chen, Tze-Jung Yeh, Mong-Hsun Tsai, Han Lin, Yen-Wenn Liu, Sheng-An Lee, Chaur-Chin Chen, Theresa Tsao, Cheng-Yan Kao. de novo assembly of RNA-Seq with efficient chimera-detection
1011 -- 1017Salvador Capella-Gutiérrez, Toni Gabaldón. Measuring guide-tree dependency of inferred gaps in progressive aligners
1018 -- 1025Alvaro J. González, Li Liao, Cathy H. Wu. Prediction of contact matrix for protein-protein interaction
1026 -- 1034Can Yang, Lin Wang, Shuqin Zhang, Hongyu Zhao. Accounting for non-genetic factors by low-rank representation and sparse regression for eQTL mapping
1035 -- 1043Ning Leng, John A. Dawson, James A. Thomson, Victor Ruotti, Anna I. Rissman, Bart M. G. Smits, Jill D. Haag, Michael N. Gould, Ron M. Stewart, Christina Kendziorski. EBSeq: an empirical Bayes hierarchical model for inference in RNA-seq experiments
1044 -- 1051Tri Hieu Nim, Le Luo, Marie-Véronique Clément, Jacob K. White, Lisa Tucker-Kellogg. Systematic parameter estimation in data-rich environments for cell signalling dynamics
1052 -- 1059Syed Murtuza Baker, C. Hart Poskar, Falk Schreiber, Björn H. Junker. An improved constraint filtering technique for inferring hidden states and parameters of a biological model
1060 -- 1067Alex Greenfield, Christoph Hafemeister, Richard Bonneau. Robust data-driven incorporation of prior knowledge into the inference of dynamic regulatory networks
1068 -- 1071Jingjing Jin, Jun Liu, Huan Wang, Limsoon Wong, Nam-Hai Chua. PLncDB: plant long non-coding RNA database
1072 -- 1075Alexey A. Gurevich, Vladislav Saveliev, Nikolay Vyahhi, Glenn Tesler. QUAST: quality assessment tool for genome assemblies
1076 -- 1077Sangwoo Kim, Kyowon Jeong, Vineet Bafna. in silico exome capture
1078 -- 1080Hasup Lee, Hahnbeom Park, Junsu Ko, Chaok Seok. GalaxyGemini: a web server for protein homo-oligomer structure prediction based on similarity
1081 -- 1082Gwenaël G. R. Leday, Mark A. van de Wiel. PLRS: a flexible tool for the joint analysis of DNA copy number and mRNA expression data
1083 -- 1085Ting Gong, Joseph D. Szustakowski. DeconRNASeq: a statistical framework for deconvolution of heterogeneous tissue samples based on mRNA-Seq data
1086 -- 1088Stephen W. Hartley, Paola Sebastiani. PleioGRiP: genetic risk prediction with pleiotropy
1089 -- 1091Nils Gehlenborg, Michael S. Noble, Gad Getz, Lynda Chin, Peter J. Park. Nozzle: a report generation toolkit for data analysis pipelines
1092 -- 1094Dong-Sheng Cao, Qing-Song Xu, Qian-Nan Hu, Yi-Zeng Liang. ChemoPy: freely available python package for computational biology and chemoinformatics
1095 -- 1097Júlio Trevisan, Plamen P. Angelov, Andrew D. Scott, Paul L. Carmichael, Francis L. Martin. IRootLab: a free and open-source MATLAB toolbox for vibrational biospectroscopy data analysis
1098 -- 1100Daniel Lobo, Taylor J. Malone, Michael Levin. Planform: an application and database of graph-encoded planarian regenerative experiments
1101 -- 1102Bo Peng, Huann-Sheng Chen, Leah E. Mechanic, Ben Racine, John Clarke, Lauren Clarke, Elizabeth Gillanders, Eric J. Feuer. Genetic Simulation Resources: a website for the registration and discovery of genetic data simulators
1103 -- 1104John Gómez, Leyla J. Garcia, Gustavo A. Salazar, Jose M. Villaveces, Swanand P. Gore, Alexander García Castro, Maria Jesus Martin, Guillaume Launay, Rafael Alcántara, Noemi del-Toro, Marine Dumousseau, Sandra E. Orchard, Sameer Velankar, Henning Hermjakob, Chenggong Zong, Peipei Ping, Manuel Corpas, Rafael C. Jimenez. BioJS: an open source JavaScript framework for biological data visualization

Volume 29, Issue 7

821 -- 829Clement Chung, Andrew Emili, Brendan J. Frey. Non-parametric Bayesian approach to post-translational modification refinement of predictions from tandem mass spectrometry
830 -- 836Susanne Balzer, Ketil Malde, Markus A. Grohme, Inge Jonassen. Filtering duplicate reads from 454 pyrosequencing data
837 -- 844Pierre-Alain Jachiet, Romain Pogorelcnik, Anne Berry, Philippe Lopez, Eric Bapteste. MosaicFinder: identification of fused gene families in sequence similarity networks
845 -- 854Sander Pronk, Szilárd Páll, Roland Schulz, Per Larsson, Pär Bjelkmar, Rossen Apostolov, Michael R. Shirts, Jeremy C. Smith, Peter M. Kasson, David van der Spoel, Berk Hess, Erik Lindahl. GROMACS 4.5: a high-throughput and highly parallel open source molecular simulation toolkit
855 -- 861Douglas E. V. Pires, Raquel Cardoso de Melo Minardi, Carlos Henrique da Silveira, Frederico F. Campos, Wagner Meira Jr.. aCSM: noise-free graph-based signatures to large-scale receptor-based ligand prediction
862 -- 869Min Chen, Miao Zang, Xinlei Wang, Guanghua Xiao. A powerful Bayesian meta-analysis method to integrate multiple gene set enrichment studies
870 -- 877Jakramate Bootkrajang, Ata Kabán. Classification of mislabelled microarrays using robust sparse logistic regression
878 -- 885Yu Zhang. A dynamic Bayesian Markov model for phasing and characterizing haplotypes in next-generation sequencing
886 -- 893Liina Kamm, Dan Bogdanov, Sven Laur, Jaak Vilo. A new way to protect privacy in large-scale genome-wide association studies
894 -- 902Yonit Hoffman, Dvir Dahary, Debora Rosa Bublik, Moshe Oren, Yitzhak Pilpel. The majority of endogenous microRNA targets within Alu elements avoid the microRNA machinery
903 -- 909Arne C. Müller, Alexander Bockmayr. Fast thermodynamically constrained flux variability analysis
910 -- 916Andrea Ocone, Andrew J. Millar, Guido Sanguinetti. Hybrid regulatory models: a statistically tractable approach to model regulatory network dynamics
917 -- 924Ahmet Emre Aladag, Cesim Erten. SPINAL: scalable protein interaction network alignment
925 -- 932Beáta Reiz, Attila Kertész-Farkas, Sándor Pongor, Michael P. Myers. Chemical rule-based filtering of MS/MS spectra
933 -- 939Matthias Zytnicki, YuFei Luo, Hadi Quesneville. Efficient comparison of sets of intervals with NC-lists
940 -- 946Brian E. Ruttenberg, Gabriel Luna, Geoffrey P. Lewis, Steven K. Fisher, Ambuj K. Singh. Quantifying spatial relationships from whole retinal images
947 -- 949Gabriel Moreno-Hagelsieb, Zilin Wang, Stephanie Walsh, Aisha ElSherbiny. Phylogenomic clustering for selecting non-redundant genomes for comparative genomics
950 -- 952Bryce Cronkite-Ratcliff, Vijay Pande. MSMExplorer: visualizing Markov state models for biomolecule folding simulations
953 -- 954Jan Kosinski, Alessandro Barbato, Anna Tramontano. MODexplorer: an integrated tool for exploring protein sequence, structure and function relationships
955 -- 956Jerome Kelleher, Nicholas H. Barton, Alison M. Etheridge. Coalescent simulation in continuous space
957 -- 959Safee Ullah Chaudhary, Sung-Young Shin, Daewon Lee, Je-Hoon Song, Kwang-Hyun Cho. ELECANS - an integrated model development environment for multiscale cancer systems biology
960 -- 962Dong-Sheng Cao, Qing-Song Xu, Yi-Zeng Liang. propy: a tool to generate various modes of Chou's PseAAC
963 -- 964Patrick Kiefer, Uwe Schmitt, Julia A. Vorholt. eMZed: an open source framework in Python for rapid and interactive development of LC/MS data analysis workflows

Volume 29, Issue 6

671 -- 677Sebastian Thieme, Philip Groth. Genome Fusion Detection: a novel method to detect fusion genes from SNP-array data
678 -- 685Tao Li, Qian-Zhong Li, Shuai Liu, Guo-Liang Fan, Yong-Chun Zuo, Yong Peng. PreDNA: accurate prediction of DNA-binding sites in proteins by integrating sequence and geometric structure information
686 -- 694Brett Trost, Anthony J. Kusalik. Computational phosphorylation site prediction in plants using random forests and organism-specific instance weights
695 -- 703Michael A. DeJesus, Yanjia J. Zhang, Christopher M. Sassetti, Eric J. Rubin, James C. Sacchettini, Thomas R. Ioerger. Bayesian analysis of gene essentiality based on sequencing of transposon insertion libraries
704 -- 710James W. J. Anderson, Pierre A. Haas, Leigh-Anne Mathieson, Vladimir Volynkin, Rune B. Lyngsø, Paula Tataru, Jotun Hein. Oxfold: kinetic folding of RNA using stochastic context-free grammars and evolutionary information
711 -- 716Jeremie Becker, Christopher Yau, John M. Hancock, Christopher C. Holmes. NucleoFinder: a statistical approach for the detection of nucleosome positions
717 -- 724Federico M. Giorgi, Cristian Del Fabbro, Francesco Licausi. Arabidopsis thaliana
725 -- 732Mark R. Christie, Jacob A. Tennessen, Michael S. Blouin. Bayesian parentage analysis with systematic accountability of genotyping error, missing data and false matching
733 -- 741Nick Dand, Frauke Sprengel, Volker Ahlers, Thomas Schlitt. BioGranat-IG: a network analysis tool to suggest mechanisms of genetic heterogeneity from exome-sequencing data
742 -- 748Dagmar Waltemath, Ron Henkel, Robert Hälke, Martin Scharm, Olaf Wolkenhauer. Improving the reuse of computational models through version control
749 -- 757Nuno D. Mendes, Frédéric Lang, Yves-Stan Le Cornec, Radu Mateescu, Grégory Batt, Claudine Chaouiya. Composition and abstraction of logical regulatory modules: application to multicellular systems
758 -- 764Cheng-Hong Yang, Yu-Huei Cheng, Li-Yeh Chuang, Hsueh-Wei Chang. Drug-SNPing: an integrated drug-based, protein interaction-based tagSNP-based pharmacogenomics platform for SNP genotyping
765 -- 771Thuc Duy Le, Lin Liu 0001, Anna Tsykin, Gregory J. Goodall, Bing Liu 0002, Bing-Yu Sun, Jiuyong Li. Inferring microRNA-mRNA causal regulatory relationships from expression data
772 -- 779Sorin Pop, Alexandre Dufour, Jean-Francois Le Garrec, Chiara V. Ragni, Clémire Cimper, Sigolene M. Meilhac, Jean-Christophe Olivo-Marin. Extracting 3D cell parameters from dense tissue environments: application to the development of the mouse heart
780 -- 789Songhua Xu, Jianqiang Sheng, Xiaonan Luo. A new algorithm for context-based biomedical diagram similarity estimation
790 -- 791Dhwani K. Desai, Harald Schunck, Johannes W. Löser, Julie LaRoche. Fragment recruitment on metabolic pathways: comparative metabolic profiling of metagenomes and metatranscriptomes
792 -- 793Petr Novák, Pavel Neumann, Jirí Pech, Jaroslav Steinhaisl, Jirí Macas. RepeatExplorer: a Galaxy-based web server for genome-wide characterization of eukaryotic repetitive elements from next-generation sequence reads
794 -- 796Xiaohua Douglas Zhang, Zhaozhi Zhang. displayHTS: a R package for displaying data and results from high-throughput screening experiments
797 -- 798Christopher S. Oehmen, Douglas J. Baxter. ScalaBLAST 2.0: rapid and robust BLAST calculations on multiprocessor systems
799 -- 801Jian Kang, Kuan-Chieh Huang, Zheng Xu, Yunfei Wang, Gonçalo R. Abecasis, Yun Li. AbCD: arbitrary coverage design for sequencing-based genetic studies
802 -- 804Michaël Vyverman, Bernard De Baets, Veerle Fack, Peter Dawyndt. essaMEM: finding maximal exact matches using enhanced sparse suffix arrays
805 -- 806Marharyta Petukh, Taylor Kimmet, Emil Alexov. BION web server: predicting non-specifically bound surface ions
807 -- 809Mieczyslaw Torchala, Iain H. Moal, Raphael A. G. Chaleil, Juan Fernández-Recio, Paul A. Bates. SwarmDock: a server for flexible protein-protein docking
810 -- 812Samuel C. Forster, Alexander M. Finkel, Jodee A. Gould, Paul J. Hertzog. RNA-eXpress annotates novel transcript features in RNA-seq data
813 -- 814Andrei Alic, José E. Pérez-Ortín, Joaquín Moreno, Vicente Arnau. mRNAStab - a web application for mRNA stability analysis
815 -- 816Mathias Ganter, Thomas Bernard, Sébastien Moretti, Jörg Stelling, Marco Pagni. MetaNetX.org: a website and repository for accessing, analysing and manipulating metabolic networks
817 -- 818Raz Shimoni, Kim Pham, Mohammed Yassin, Min Gu, Sarah M. Russell. TACTICS, an interactive platform for customized high-content bioimaging analysis
819 -- 0Chris J. Oates, Bryan T. J. Hennessy, Yiling Lu, Gordon B. Mills, Sach Mukherjee. Network inference using steady-state data and Goldbeter-Koshland kinetics

Volume 29, Issue 5

533 -- 541Hyungwon Choi, Damian Fermin, Alexey I. Nesvizhskii, Debashis Ghosh, Zhaohui S. Qin. Sparsely correlated hidden Markov models with application to genome-wide location studies
542 -- 550Niclas Thomas, James Heather, Wilfred Ndifon, John Shawe-Taylor, Benjamin Chain. Decombinator: a tool for fast, efficient gene assignment in T-cell receptor sequences using a finite state machine
551 -- 560Georg Sauthoff, Mathias Möhl, Stefan Janssen, Robert Giegerich. Bellman's GAP - a language and compiler for dynamic programming in sequence analysis
561 -- 570François Chevenet, Matthieu Jung, Martine Peeters, Tulio de Oliveira, Olivier Gascuel. Searching for virus phylotypes
571 -- 579Mukul S. Bansal, Guy Banay, Timothy J. Harlow, J. Peter Gogarten, Ron Shamir. Systematic inference of highways of horizontal gene transfer in prokaryotes
580 -- 587Nikolas S. Burkoff, Csilla Várnai, David L. Wild. Predicting protein β-sheet contacts using a maximum entropy-based correlated mutation measure
588 -- 596Tim Wiegels, Stefan Bienert, Andrew E. Torda. Fast alignment and comparison of RNA structures
597 -- 604Mu Gao, Jeffrey Skolnick. APoc: large-scale identification of similar protein pockets
605 -- 613Pan Tong, Yong Chen, Xiao Su, Kevin R. Coombes. SIBER: systematic identification of bimodally expressed genes using RNAseq data
614 -- 621David G. Knowles, Maik Röder, Angelika Merkel, Roderic Guigó. Grape RNA-Seq analysis pipeline environment
622 -- 629Christopher L. Poirel, Ahsanur Rahman, Richard R. Rodrigues, Arjun Krishnan, Jacqueline R. Addesa, T. M. Murali. Reconciling differential gene expression data with molecular interaction networks
630 -- 637Duc-Hau Le, Yung-Keun Kwon. A coherent feedforward loop design principle to sustain robustness of biological networks
638 -- 644Boya Xie, Qin Ding, Hongjin Han, Di Wu. miRCancer: a microRNA-cancer association database constructed by text mining on literature
645 -- 646Chengjun Zhang, Jun Wang, Manyuan Long, Chuanzhu Fan. gKaKs: the pipeline for genome-level Ka/Ks calculation
647 -- 648Christopher Douville, Hannah Carter, Rick Kim, Noushin Niknafs, Mark Diekhans, Peter D. Stenson, David N. Cooper, Michael C. Ryan, Rachel Karchin. CRAVAT: cancer-related analysis of variants toolkit
649 -- 651Jing-Woei Li, Raymond Wan, Chi-Shing Yu, Ngai Na Co, Nathalie Wong, Ting-Fung Chan. ViralFusionSeq: accurately discover viral integration events and reconstruct fusion transcripts at single-base resolution
652 -- 653Guillaume Rizk, Dominique Lavenier, Rayan Chikhi. k-mer counting with very low memory usage
654 -- 655Preeti Arunapuram, Ingolfur Edvardsson, Michael Golden, James W. J. Anderson, Ádám Novák, Zsuzsanna Sükösd, Jotun Hein. StatAlign 2.0: combining statistical alignment with RNA secondary structure prediction
656 -- 657Michele A. Busby, Chip Stewart, Chase A. Miller, Krzysztof R. Grzeda, Gabor T. Marth. Scotty: a web tool for designing RNA-Seq experiments to measure differential gene expression
658 -- 660Zuguang Gu, Jin Wang. CePa: an R package for finding significant pathways weighted by multiple network centralities
661 -- 663Gabriela Bindea, Jérôme Galon, Bernhard Mlecnik. in silico data
664 -- 665Richard Adams, Allan Clark, Azusa Yamaguchi, Neil Hanlon, Nikos Tsorman, Shakir Ali, Galina Lebedeva, Alexey Goltsov, Anatoly A. Sorokin, Ozgur E. Akman, Carl Troein, Andrew J. Millar, Igor Goryanin, Stephen Gilmore. SBSI: an extensible distributed software infrastructure for parameter estimation in systems biology
666 -- 668Markus S. Schröder, Daniel Gusenleitner, John Quackenbush, Aedín C. Culhane, Benjamin Haibe-Kains. RamiGO: an R/Bioconductor package providing an AmiGO Visualize interface
669 -- 0Mark Silberstein, Omer Weissbrod, Lars Otten, Anna Tzemach, Andrei Anisenia, Oren Shtark, Dvir Tuberg, Eddie Galfrin, Irena Gannon, Adel Shalata, Zvi U. Borochowitz, Rina Dechter, Elizabeth Thompson, Dan Geiger. A system for exact and approximate genetic linkage analysis of SNP data in large pedigrees

Volume 29, Issue 4

413 -- 419Alan Medlar, Dorota Glowacka, Horia Stanescu, Kevin Bryson, Robert Kleta. SwiftLink: parallel MCMC linkage analysis using multicore CPU and GPU
420 -- 427Jia-Shing Chen, Wei-Shiang Hung, Hsiang-Han Chan, Shaw-Jenq Tsai, H. Sunny Sun. In silico identification of oncogenic potential of fyn-related kinase in hepatocellular carcinoma
428 -- 434Nilgun Donmez, Michael Brudno. SCARPA: scaffolding reads with practical algorithms
435 -- 443Scott C. Clark, Rob Egan, Peter I. Frazier, Zhong Wang. ALE: a generic assembly likelihood evaluation framework for assessing the accuracy of genome and metagenome assemblies
444 -- 450Parameswaran Ramachandran, Gareth A. Palidwor, Christopher J. Porter, Theodore J. Perkins. MaSC: mappability-sensitive cross-correlation for estimating mean fragment length of single-end short-read sequencing data
451 -- 460Mengjie Chen, Valentina Svicher, Anna Artese, Giosuè Costa, Claudia Alteri, Francesco Ortuso, Lucia Parrotta, Yang Liu, Chang Liu, Carlo-Federico Perno, Stefano Alcaro, Jing Zhang 0010. Detecting and understanding genetic and structural features in HIV-1 B subtype V3 underlying HIV-1 co-receptor usage
461 -- 467Andrew McDavid, Greg Finak, Pratip K. Chattopadhyay, Maria Dominguez, Laurie Lamoreaux, Steven S. Ma, Mario Roederer, Raphael Gottardo. Data exploration, quality control and testing in single-cell qPCR-based gene expression experiments
468 -- 475Rosario M. Piro, Ivan Molineris, Ferdinando Di Cunto, Roland Eils, Rainer König. Disease-gene discovery by integration of 3D gene expression and transcription factor binding affinities
476 -- 482Jesse Gillis, Paul Pavlidis. Assessing identity, redundancy and confounds in Gene Ontology annotations over time
483 -- 491Wayne Hayes, Kai Sun, Natasa Przulj. Graphlet-based measures are suitable for biological network comparison
492 -- 493Jianrong Wang, Victoria V. Lunyak, I. King Jordan. BroadPeak: a novel algorithm for identifying broad peaks in diffuse ChIP-seq datasets
494 -- 496Marcus R. Breese, Yunlong Liu. NGSUtils: a software suite for analyzing and manipulating next-generation sequencing datasets
497 -- 498Jed Zaretzki, Charles Bergeron, Tao-Wei Huang, Patrik Rydberg, S. Joshua Swamidass, Curt M. Breneman. RS-WebPredictor: a server for predicting CYP-mediated sites of metabolism on drug-like molecules
499 -- 503Timothy P. Levine, Rachel D. Daniels, Alberto T. Gatta, Louise H. Wong, Matthew J. Hayes. The product of C9orf72, a gene strongly implicated in neurodegeneration, is structurally related to DENN Rab-GEFs
504 -- 505Castrense Savojardo, Piero Fariselli, Rita Casadio. BETAWARE: a machine-learning tool to detect and predict transmembrane beta-barrel proteins in prokaryotes
506 -- 508Clemens Wrzodek, Johannes Eichner, Finja Büchel, Andreas Zell. InCroMAP: integrated analysis of cross-platform microarray and pathway data
509 -- 510Daniel Bottomly, Beth Wilmot, Jeffrey W. Tyner, Christopher A. Eide, Marc M. Loriaux, Brian J. Druker, Shannon K. McWeeney. HitWalker: variant prioritization for personalized functional cancer genomics
511 -- 512Linnea Järvstråt, Mikael Johansson, Urban Gullberg, Björn Nilsson. Ultranet: efficient solver for the sparse inverse covariance selection problem in gene network modeling
513 -- 514Marco Antoniotti, Gary D. Bader, Giulio Caravagna, Silvia Crippa, Alex Graudenzi, Giancarlo Mauri. GeStoDifferent: a Cytoscape plugin for the generation and the identification of gene regulatory networks describing a stochastic cell differentiation process
515 -- 517Woonghee Lee, Arash Bahrami, John L. Markley. ADAPT-NMR Enhancer: complete package for reduced dimensionality in protein NMR spectroscopy
518 -- 519Arsen Arakelyan, Lilit Nersisyan. KEGGParser: parsing and editing KEGG pathway maps in Matlab
520 -- 522Frank Kramer, Michaela Bayerlová, Florian Klemm, Annalen Bleckmann, Tim Beißbarth. rBiopaxParser - an R package to parse, modify and visualize BioPAX data
523 -- 524Nikolas Fechner, George Papadatos, David Evans, John Richard Morphy, Suzanne Clare Brewerton, David Thorner, Michael Bodkin. ChEMBLSpace - a graphical explorer of the chemogenomic space covered by the ChEMBL database
525 -- 527Eamonn Maguire, Alejandra González Beltrán, Patricia L. Whetzel, Susanna-Assunta Sansone, Philippe Rocca-Serra. OntoMaton: a Bioportal powered ontology widget for Google Spreadsheets
528 -- 531Qing Duan, Eric Yi Liu, Damien C. Croteau-Chonka, Karen L. Mohlke, Yun Li. A comprehensive SNP and indel imputability database

Volume 29, Issue 3

299 -- 307Shengping Yang, Stanley Pounds, Kun Zhang, Zhide Fang. PAIR: paired allelic log-intensity-ratio-based normalization method for SNP-CGH arrays
308 -- 315Yongchao Liu, Jan Schröder, Bertil Schmidt. k-mer spectrum-based error corrector for Illumina sequence data
316 -- 321Paul M. Gontarz, Jennifer Berger, Chung F. Wong. SRmapper: a fast and sensitive genome-hashing alignment tool
322 -- 330Takako Takeda, Rosario I. Corona, Jun-tao Guo. A knowledge-based orientation potential for transcription factor-DNA docking
331 -- 337Orly Noivirt-Brik, Gershon Hazan, Ron Unger, Yanay Ofran. Non-local residue-residue contacts in proteins are more conserved than local ones
338 -- 346Liming Wang, Xiaodong Wang, Adam P. Arkin, Michael S. Samoilov. Inference of gene regulatory networks from genome-wide knockout fitness data
347 -- 354Yuan Shi, Gregory Mellier, Sinong Huang, Jacob White, Shazib Pervaiz, Lisa Tucker-Kellogg. Computational modelling of LY303511 and TRAIL-induced apoptosis suggests dynamic regulation of cFLIP
355 -- 364Chengwei Lei, Jianhua Ruan. A novel link prediction algorithm for reconstructing protein-protein interaction networks by topological similarity
365 -- 372Yoshihiko Matsuta, Masahiro Ito, Yukako Tohsato. ECOH: An Enzyme Commission number predictor using mutual information and a support vector machine
373 -- 380Fernando Amat, Eugene W. Myers, Philipp J. Keller. Fast and robust optical flow for time-lapse microscopy using super-voxels
381 -- 383Chase A. Miller, Jon Anthony, Michelle M. Meyer, Gabor T. Marth. Scribl: an HTML5 Canvas-based graphics library for visualizing genomic data over the web
384 -- 386Theodore R. Pak, Frederick P. Roth. ChromoZoom: a flexible, fluid, web-based genome browser
387 -- 388Connor McCoy, Aaron Gallagher, Noah G. Hoffman, Frederick A. Matsen. nestly - a framework for running software with nested parameter choices and aggregating results
389 -- 390Thomas M. Keane, Kim Wong, David J. Adams. RetroSeq: transposable element discovery from next-generation sequencing data
391 -- 392Raeece Naeem, Mamoon Rashid, Arnab Pain. READSCAN: a fast and scalable pathogen discovery program with accurate genome relative abundance estimation
393 -- 394Lane Votapka, Rommie E. Amaro. Multistructural hot spot characterization with FTProd
395 -- 397Anna Maria Gallina, Paola Bisignano, Maurizio Bergamino, Domenico Bordo. PLI: a web-based tool for the comparison of protein-ligand interactions observed on PDB structures
398 -- 399Mickaël Krzeminski, Joseph A. Marsh, Chris Neale, Wing Yiu Choy, Julie D. Forman-Kay. Characterization of disordered proteins with ENSEMBLE
400 -- 401Brad Reisfeld, Jaime H. Ivy, Michael A. Lyons, Jesse M. Wright, Justin L. Rogers, Arthur N. Mayeno. DoseSim: a tool for pharmacokinetic/pharmacodynamic analysis and dose reconstruction
402 -- 403David M. Reif, Myroslav Sypa, Eric F. Lock, Fred A. Wright, Ander Wilson, Tommy Cathey, Richard R. Judson, Ivan Rusyn. ToxPi GUI: an interactive visualization tool for transparent integration of data from diverse sources of evidence
404 -- 406Gang Liu, Apurv Puri, Sriram Neelamegham. Glycosylation Network Analysis Toolbox: a MATLAB-based environment for systems glycobiology
407 -- 408Davide Albanese, Michele Filosi, Roberto Visintainer, Samantha Riccadonna, Giuseppe Jurman, Cesare Furlanello. minerva and minepy: a C engine for the MINE suite and its R, Python and MATLAB wrappers
409 -- 411Xinyi Liu, Shuyuan Wang, Fanlin Meng, Jizhe Wang, Yan Zhang, Enyu Dai, Xuexin Yu, Xia Li, Wei Jiang. SM2miR: a database of the experimentally validated small molecules' effects on microRNA expression
412 -- 0Oliver Serang. Concerning the accuracy of Fido and parameter choice

Volume 29, Issue 24

3107 -- 3108Christian Theil Have, Lars Juhl Jensen. Are graph databases ready for bioinformatics?
3109 -- 3112Daudi Jjingo, Jianrong Wang, Andrew B. Conley, Victoria V. Lunyak, I. King Jordan. cis-regulatory elements with both boundary and enhancer sequences in the human genome
3113 -- 3120Elizabeth Purdom, Christine Ho, Catherine S. Grasso, Michael Quist, Raymond J. Cho, Paul T. Spellman. Methods and challenges in timing chromosomal abnormalities within cancer samples
3121 -- 3127Bernhard Haubold, Linda Krause, Thomas Horn, Peter Pfaffelhuber. An alignment-free test for recombination
3128 -- 3134Pasi Rastas, Lars Paulin, Ilkka Hanski, Rainer Lehtonen, Petri Auvinen. Lep-MAP: fast and accurate linkage map construction for large SNP datasets
3135 -- 3142Lingyun Zou, Chonghan Nan, Fuquan Hu. Accurate prediction of bacterial type IV secreted effectors using amino acid composition and PSSM profiles
3143 -- 3150Tobias Marschall, Iman Hajirasouliha, Alexander Schönhuth. MATE-CLEVER: Mendelian-inheritance-aware discovery and genotyping of midsize and long indels
3151 -- 3157Castrense Savojardo, Piero Fariselli, Pier Luigi Martelli, Rita Casadio. BCov: a method for predicting β-sheet topology using sparse inverse covariance estimation and integer programming
3158 -- 3166Guang Qiang Dong, Hao Fan, Dina Schneidman-Duhovny, Ben M. Webb, Andrej Sali. Optimized atomic statistical potentials: assessment of protein interfaces and loops
3167 -- 3173Kourosh Zarringhalam, Ahmed Enayetallah, Alex Gutteridge, Ben Sidders, Daniel Ziemek. Molecular causes of transcriptional response: a Bayesian prior knowledge approach
3174 -- 3180Anastasia Deckard, Ron C. Anafi, John B. Hogenesch, Steven B. Haase, John Harer. Design and analysis of large-scale biological rhythm studies: a comparison of algorithms for detecting periodic signals in biological data
3181 -- 3190Ciarán P. Fisher, Nicholas J. Plant, J. Bernadette Moore, Andrzej M. Kierzek. QSSPN: dynamic simulation of molecular interaction networks describing gene regulation, signalling and whole-cell metabolism in human cells
3191 -- 3198Kai-Cheng Hsu, Feng-Sheng Wang. Fuzzy optimization for detecting enzyme targets of human uric acid metabolism
3199 -- 3203Sven Degroeve, Lennart Martens. 2PIP: a tool for MS/MS peak intensity prediction
3204 -- 3210Tao Wang, Jie Liu, Li Shen, Julian Tonti-Filippini, Yun Zhu, Haiyang Jia, Ryan Lister, John W. Whitaker, Joseph R. Ecker, A. Harvey Millar, Bing Ren, Wei Wang. STAR: an integrated solution to management and visualization of sequencing data
3211 -- 3219Magdalena Przydzial, Barun Bhhatarai, Amar Koleti, Uma Vempati, Stephan C. Schürer. GPCR ontology: development and application of a G protein-coupled receptor pharmacology knowledge framework
3220 -- 3221Melanie A. Huntley, Jessica L. Larson, Christina Chaivorapol, Gabriel Becker, Michael Lawrence, Jason A. Hackney, Joshua S. Kaminker. ReportingTools: an automated result processing and presentation toolkit for high-throughput genomic analyses
3222 -- 3224Yanbo Ye, Bo Wei, Lei Wen, Simon Rayner. BlastGraph: a comparative genomics tool based on BLAST and graph algorithms
3225 -- 3226Dadi Gao, Robert Middleton, John E. J. Rasko, William Ritchie. miREval 2.0: a web tool for simple microRNA prediction in genome sequences
3227 -- 3229Xueqiu Lin, Deqiang Sun, Benjamin Rodriguez, Qian Zhao, Hanfei Sun, Yong Zhang, Wei Li. BSeQC: quality control of bisulfite sequencing experiments
3230 -- 3231Rui C. Chaves, Jean-Luc Pellequer. DockAFM: benchmarking protein structures by docking under AFM topographs
3232 -- 3234Jianguo Xia, Ngan H. Lyle, Matthew L. Mayer, Olga M. Pena, Robert E. W. Hancock. INVEX - a web-based tool for integrative visualization of expression data
3235 -- 3237Xiaojing Wang, Bing Zhang. customProDB: an R package to generate customized protein databases from RNA-Seq data for proteomics search
3238 -- 3240Wenchao Jiang, Pinghao Li, Shuang Wang, Yuan Wu, Meng Xue, Lucila Ohno-Machado, Xiaoqian Jiang. WebGLORE: a Web service for Grid LOgistic REgression
3241 -- 3242Thomas Cokelaer, Dennis Pultz, Lea M. Harder, Jordi Serra-Musach, Julio Saez-Rodriguez. BioServices: a common Python package to access biological Web Services programmatically
3243 -- 3245Burkhard Rost. ISCB: past-present perspective for the International Society for Computational Biology
3246 -- 3247. ISCB/SPRINGER series in computational biology

Volume 29, Issue 23

2959 -- 2963Mark Howison, Felipe Zapata, Casey W. Dunn. de novo sequence assembly
2964 -- 2970Gary K. Chen, Xiao Chang, Christina Curtis, Kai Wang. Precise inference of copy number alterations in tumor samples from SNP arrays
2971 -- 2978Jikun Wu, Wenqian Zhang, Songbo Huang, Zengquan He, Yanbing Cheng, Jun Wang, Tak Wah Lam, Zhiyu Peng, Siu-Ming Yiu. SOAPfusion: a robust and effective computational fusion discovery tool for RNA-seq reads
2979 -- 2986Haitham Ashoor, Aurélie Hérault, Aurélie Kamoun, François Radvanyi, Vladimir B. Bajic, Emmanuel Barillot, Valentina Boeva. HMCan: a method for detecting chromatin modifications in cancer samples using ChIP-seq data
2987 -- 2994Ashok Rajaraman, Eric Tannier, Cedric Chauve. FPSAC: fast phylogenetic scaffolding of ancient contigs
2995 -- 3002Adam B. Olshen, Andrew C. Hsieh, Craig R. Stumpf, Richard A. Olshen, Davide Ruggero, Barry S. Taylor. Assessing gene-level translational control from ribosome profiling
3003 -- 3006Brent S. Pedersen, Ivana V. Yang, Subhajyoti De. CruzDB: software for annotation of genomic intervals with UCSC genome-browser database
3007 -- 3013Lauren J. Mills, William R. Pearson. Adjusting scoring matrices to correct overextended alignments
3014 -- 3019Henrik Nordberg, Karan Bhatia, Kai Wang, Zhong Wang. BioPig: a Hadoop-based analytic toolkit for large-scale sequence data
3020 -- 3028Miguel Arenas, Helena G. Dos Santos, David Posada, Ugo Bastolla. Protein evolution along phylogenetic histories under structurally constrained substitution models
3029 -- 3035Jan-Oliver Janda, Andreas Meier, Rainer Merkl. CLIPS-4D: a classifier that distinguishes structurally and functionally important residue-positions based on sequence and 3D data
3036 -- 3044Young-Suk Lee, Arjun Krishnan, Qian Zhu, Olga G. Troyanskaya. Ontology-aware classification of tissue and cell-type signals in gene expression profiles across platforms and technologies
3045 -- 3052Naama Tepper, Tomer Shlomi. An integrated computational approach for metabolic flux analysis coupled with inference of tandem-MS collisional fragments
3053 -- 3059David duVerle, Ichiro Takeuchi, Yuko Murakami-Tonami, Kenji Kadomatsu, Koji Tsuda. Discovering combinatorial interactions in survival data
3060 -- 3066Yawwani Gunawardana, Mahesan Niranjan. Bridging the gap between transcriptome and proteome measurements identifies post-translationally regulated genes
3067 -- 3072Carl Murie, Caroline Barette, Laurence Lafanechère, Robert Nadon. Single assay-wide variance experimental (SAVE) design for high-throughput screening
3073 -- 3079David Gfeller, Olivier Michielin, Vincent Zoete. Shaping the interaction landscape of bioactive molecules
3080 -- 3086Johan Nyström-Persson, Yoshinobu Igarashi, Maori Ito, Mizuki Morita, Noriyuki Nakatsu, Hiroshi Yamada, Kenji Mizuguchi. Toxygates: interactive toxicity analysis on a hybrid microarray and linked data platform
3087 -- 3093Cemal Cagatay Bilgin, Sun Kim, Elle Leung, Hang Chang, Bahram Parvin. Integrated profiling of three dimensional cell culture models and 3D microscopy
3094 -- 3096Thérèse A. Holton, Gianluca Pollastri, Denis C. Shields, Catherine Mooney. CPPpred: prediction of cell penetrating peptides
3097 -- 3099Weichun Huang, Rasiah Loganantharaj, Bryce Schroeder, David Fargo, Leping Li. PAVIS: a tool for Peak Annotation and Visualization
3100 -- 3101Charles E. Robertson, J. Kirk Harris, Brandie D. Wagner, David Granger, Kathy Browne, Beth Tatem, Leah M. Feazel, Kristin Park, Norman R. Pace, Daniel N. Frank. Explicet: graphical user interface software for metadata-driven management, analysis and visualization of microbiome data
3102 -- 3104Thomas Schnattinger, Uwe Schöning, Anita Marchfelder, Hans A. Kestler. RNA-Pareto: interactive analysis of Pareto-optimal RNA sequence-structure alignments
3105 -- 3106Oksana Sorokina, Anatoly A. Sorokin, J. Douglas Armstrong, Vincent Danos. A simulator for spatially extended kappa models

Volume 29, Issue 22

2813 -- 2821Caihong Zheng, Xuexia Miao, Yanen Li, Ying Huang, Jue Ruan, Xi Ma, Li Wang, Chung-I. Wu, Jun Cai. Determination of genomic copy number alteration emphasizing a restriction site-based strategy of genome re-sequencing
2822 -- 2825Keiko Sato, Toshihide Hara, Masanori Ohya. The code structure of the p53 DNA-binding domain and the prognosis of breast cancer patients
2826 -- 2834Jurgen F. Nijkamp, Mihai Pop, Marcel J. T. Reinders, Dick de Ridder. Exploring variation-aware contig graphs for (comparative) metagenomics using MaryGold
2835 -- 2843Kaname Kojima, Naoki Nariai, Takahiro Mimori, Mamoru Takahashi, Yumi Yamaguchi-Kabata, Yukuto Sato, Masao Nagasaki. A statistical variant calling approach from pedigree information and local haplotyping with phase informative reads
2844 -- 2851Lauren A. Sugden, Michael R. Tackett, Yiannis A. Savva, William A. Thompson, Charles E. Lawrence. Assessing the validity and reproducibility of genome-scale predictions
2852 -- 2858Cristian O. Rohr, R. Gonzalo Parra, Patricio Yankilevich, Carolina Perez-Castro. INSECT: IN-silico SEarch for Co-occurring Transcription factors
2859 -- 2868Feng Zeng, Rui Jiang, Ting Chen. PyroHMMvar: a sensitive and accurate method to call short indels and SNPs for Ion Torrent and 454 data
2869 -- 2876Jiajie Zhang, Paschalia Kapli, Pavlos Pavlidis, Alexandros Stamatakis. A general species delimitation method with applications to phylogenetic placements
2877 -- 2883Sarah E. Reese, Kellie J. Archer, Terry M. Therneau, Elizabeth J. Atkinson, Celine M. Vachon, Mariza de Andrade, Jean-Pierre Kocher, Jeanette E. Eckel-Passow. A new statistic for identifying batch effects in high-throughput genomic data that uses guided principal component analysis
2884 -- 2891Tamar Sofer, Elizabeth D. Schifano, Jane A. Hoppin, Lifang Hou, Andrea A. Baccarelli. A-clustering: a novel method for the detection of co-regulated methylation regions, and regions associated with exposure
2892 -- 2899Adi L. Tarca, Mario Lauria, Michael Unger, Erhan Bilal, Stéphanie Boué, Kushal Kumar Dey, Julia Hoeng, Heinz Koeppl, Florian Martin, Pablo Meyer, Preetam Nandy, Raquel Norel, Manuel C. Peitsch, John Jeremy Rice, Roberto Romero, Gustavo Stolovitzky, Marja Talikka, Yang Xiang, Christoph Zechner, Improver Dsc Collaborators. Strengths and limitations of microarray-based phenotype prediction: lessons learned from the IMPROVER Diagnostic Signature Challenge
2900 -- 2908Brian J. Schmidt, Ali Ebrahim, Thomas O. Metz, Joshua N. Adkins, Bernhard Ø. Palsson, Daniel R. Hyduke. 3E: condition-specific models of cellular metabolism developed from metabolomics and expression data
2909 -- 2917Robert Leaman, Rezarta Islamaj Dogan, Zhiyong Lu. DNorm: disease name normalization with pairwise learning to rank
2918 -- 2924Raul Rodriguez-Esteban, William Loging. Quantifying the complexity of medical research
2925 -- 2927Donghyung Lee, T. Bernard Bigdeli, Brien P. Riley, Ayman H. Fanous, Silviu-Alin Bacanu. DIST: direct imputation of summary statistics for unmeasured SNPs
2928 -- 2930Federico Agostini, Andreas Zanzoni, Petr Klus, Domenica Marchese, Davide Cirillo, Gian Gaetano Tartaglia. omics: a web server for large-scale prediction of protein-RNA interactions
2931 -- 2932Jan Grau, Jens Boch, Stefan Posch. TALENoffer: genome-wide TALEN off-target prediction
2933 -- 2935Eric P. Nawrocki, Sean R. Eddy. Infernal 1.1: 100-fold faster RNA homology searches
2936 -- 2937David Gordon, Phil Green. Consed: a graphical editor for next-generation sequencing
2938 -- 2940Lina Weinbrand, Assaf Avihoo, Danny Barash. RNAfbinv: an interactive Java application for fragment-based design of RNA sequences
2941 -- 2942Nikolai Hecker, Tim Wiegels, Andrew E. Torda. RNA secondary structure diagrams for very large molecules: RNAfdl
2943 -- 2945Shintaro Katayama, Virpi Töhönen, Sten Linnarsson, Juha Kere. SAMstrt: statistical test for differential expression in single-cell transcriptome with spike-in normalization
2946 -- 2947Elizabeth A. McClellan, Perry D. Moerland, Peter van der Spek, Andrew Stubbs. R package for integrative biological network analysis with mass spectrometry data
2948 -- 2949Ryan M. Taylor, Jamison Dance, Russ J. Taylor, John T. Prince. Metriculator: quality assessment for mass spectrometry-based proteomics
2950 -- 2952Hae-Min Park, Ju-Hyeong Park, Yoon-Woo Kim, Kyoung-Jin Kim, Hee-Jin Jeong, Kyoung-Soon Jang, Byung-Gee Kim, Yun-Gon Kim. The Xeno-glycomics database (XDB): a relational database of qualitative and quantitative pig glycome repertoire
2953 -- 2954Renkai Ji, Qian Cong, Wenlin Li, Nick V. Grishin. M2SG: mapping human disease-related genetic variants to protein sequences and genomic loci
2955 -- 2957Ilinca Tudose, Janna Hastings, Venkatesh Muthukrishnan, Gareth Owen, Steve Turner, Adriano Dekker, Namrata Kale, Marcus Ennis, Christoph Steinbeck. OntoQuery: easy-to-use web-based OWL querying
2958 -- 0Christophe Lemetre, Quanwei Zhang, Zhengdong D. Zhang. SubNet: a Java application for subnetwork extraction

Volume 29, Issue 21

2669 -- 2677Aleksey V. Zimin, Guillaume Marçais, Daniela Puiu, Michael Roberts, Steven L. Salzberg, James A. Yorke. The MaSuRCA genome assembler
2678 -- 2682Liangcai Zhang, Li Zhang. Use of autocorrelation scanning in DNA copy number analysis
2683 -- 2689Gwo-Liang Chen, Yun-Juan Chang, Chun-Hway Hsueh. ab initio software package for automated genome-wide analysis of DNA repeats for prokaryotes
2690 -- 2698Jie Ren, Kai Song, Fengzhu Sun, Minghua Deng, Gesine Reinert. Multiple alignment-free sequence comparison
2699 -- 2704Rafik A. Salama, Dov J. Stekel. A non-independent energy-based multiple sequence alignment improves prediction of transcription factor binding sites
2705 -- 2713Anaïs F. Bardet, Jonas Steinmann, Sangeeta Bafna, Juergen A. Knoblich, Julia Zeitlinger, Alexander Stark. Identification of transcription factor binding sites from ChIP-seq data at high resolution
2714 -- 2721Angela D. Wilkins, Eric Venner, David C. Marciano, Serkan Erdin, Benu Atri, Rhonald C. Lua, Olivier Lichtarge. Accounting for epistatic interactions improves the functional analysis of protein structures
2722 -- 2728Valerio Mariani, Marco Biasini, Alessandro Barbato, Torsten Schwede. lDDT: a local superposition-free score for comparing protein structures and models using distance difference tests
2729 -- 2734Sébastien Artigaud, Olivier Gauthier, Vianney Pichereau. Identifying differentially expressed proteins in two-dimensional electrophoresis experiments: inputs from transcriptomics statistical tools
2735 -- 2743Ashok Reddy Dinasarapu, Shakti Gupta, Mano Ram Maurya, Eoin Fahy, Jun Min, Manish Sud, Merril J. Gersten, Christopher K. Glass, Shankar Subramaniam. A combined omics study on activated macrophages - enhanced role of STATs in apoptosis, immunity and lipid metabolism
2744 -- 2749Qing Duan, Eric Yi Liu, Paul L. Auer, Guosheng Zhang, Ethan M. Lange, Goo Jun, Chris Bizon, Shuo Jiao, Steven Buyske, Nora Franceschini, Chris S. Carlson, Li Hsu, Alex P. Reiner, Ulrike Peters, Jeffrey Haessler, Keith Curtis, Christina L. Wassel, Jennifer G. Robinson, Lisa W. Martin, Christopher A. Haiman, Loic Le Marchand, Tara Cox Matise, Lucia A. Hindorff, Dana C. Crawford, Themistocles L. Assimes, Hyun Min Kang, Gerardo Heiss, Rebecca D. Jackson, Charles Kooperberg, James G. Wilson, Gonçalo R. Abecasis, Kari E. North, Deborah A. Nickerson, Leslie A. Lange, Yun Li. Imputation of coding variants in African Americans: better performance using data from the exome sequencing project
2744 -- 2749Qing Duan, Eric Yi Liu, Paul L. Auer, Guosheng Zhang, Ethan M. Lange, Goo Jun, Chris Bizon, Shuo Jiao, Steven Buyske, Nora Franceschini, Chris S. Carlson, Li Hsu, Alex P. Reiner, Ulrike Peters, Jeffrey Haessler, Keith Curtis, Christina L. Wassel, Jennifer G. Robinson, Lisa W. Martin, Christopher A. Haiman, Loic Le Marchand, Tara Cox Matise, Lucia A. Hindorff, Dana C. Crawford, Themistocles L. Assimes, Hyun Min Kang, Gerardo Heiss, Rebecca D. Jackson, Charles Kooperberg, James G. Wilson, Gonçalo R. Abecasis, Kari E. North, Deborah A. Nickerson, Leslie A. Lange, Yun Li. Imputation of coding variants in African Americans: better performance using data from the exome sequencing project
2750 -- 2756James J. Yang, Jia Li, Anne Buu, L. K. Williams. Efficient inference of local ancestry
2757 -- 2764Evan O. Paull, Daniel E. Carlin, Mario Niepel, Peter K. Sorger, David Haussler, Joshua M. Stuart. Discovering causal pathways linking genomic events to transcriptional states using Tied Diffusion Through Interacting Events (TieDIE)
2765 -- 2773Leonid Chindelevitch, Cheng-Yu Ma, Chung-Shou Liao, Bonnie Berger. Optimizing a global alignment of protein interaction networks
2774 -- 2780Tsung-Heng Tsai, Mahlet G. Tadesse, Cristina Di Poto, Lewis K. Pannell, Yehia Mechref, Yue Joseph Wang, Habtom W. Ressom. Multi-profile Bayesian alignment model for LC-MS data analysis with integration of internal standards
2781 -- 2787João D. Ferreira, Janna Hastings, Francisco M. Couto. Exploiting disjointness axioms to improve semantic similarity measures
2788 -- 2789Ben Elsworth, Martin O. Jones, Mark L. Blaxter. Badger - an accessible genome exploration environment
2790 -- 2791Fritz J. Sedlazeck, Philipp Rescheneder, Arndt von Haeseler. NextGenMap: fast and accurate read mapping in highly polymorphic genomes
2792 -- 2794Yan Wang, Tyler W. H. Backman, Kevin Horan, Thomas Girke. fmcsR: mismatch tolerant maximum common substructure searching in R
2795 -- 2796Benjamin Lutz, Claude Sinner, Geertje Heuermann, Abhinav Verma, Alexander Schug. eSBMTools 1.0: enhanced native structure-based modeling tools
2797 -- 2798Greg C. Imholte, Marie-Pier Scott-Boyer, Aurélie Labbe, Christian F. Deschepper, Raphael Gottardo. iBMQ: a R/Bioconductor package for integrated Bayesian modeling of eQTL data
2799 -- 2800Amit Kumar Yadav, Puneet Kumar Kadimi, Dhirendra Kumar, Debasis Dash. ProteoStats - a library for estimating false discovery rates in proteomics pipelines
2801 -- 2803Jesse D. Ziebarth, Anindya Bhattacharya, Yan Cui. Bayesian Network Webserver: a comprehensive tool for biological network modeling
2804 -- 2805Kevin L. Crowell, Gordon W. Slysz, Erin S. Baker, Brian L. LaMarche, Matthew E. Monroe, Yehia M. Ibrahim, Samuel H. Payne, Gordon A. Anderson, Richard D. Smith. LC-IMS-MS Feature Finder: detecting multidimensional liquid chromatography, ion mobility and mass spectrometry features in complex datasets
2806 -- 2807Christina M. Bergey, Andrew M. Watkins, Paramjit S. Arora. HippDB: a database of readily targeted helical protein-protein interactions
2808 -- 2809Chuming Chen, Zhiwen Li, Hongzhan Huang, Baris E. Suzek, Cathy H. Wu, UniProt Consortium. A fast Peptide Match service for UniProt Knowledgebase
2810 -- 2811Cristóbal Fresno, Elmer Andrés Fernández. R interface to DAVID

Volume 29, Issue 20

2521 -- 2523Luiz Felipe Valter de Oliveira, Ana Paula Christoff, Rogerio Margis. isomiRID: a framework to identify microRNA isoforms
2524 -- 2528Junichi Iwakiri, Tomoshi Kameda, Kiyoshi Asai, Michiaki Hamada. Analysis of base-pairing probabilities of RNA molecules involved in protein-RNA interactions
2529 -- 2538Jonas Behr, André Kahles, Yi Zhong, Vipin T. Sreedharan, Philipp Drewe, Gunnar Rätsch. MITIE: Simultaneous RNA-Seq-based transcript identification and quantification in multiple samples
2539 -- 2546Mikhail Shugay, Iñigo Ortiz de Mendíbil, José L. Vizmanos, Francisco J. Novo. Oncofuse: a computational framework for the prediction of the oncogenic potential of gene fusions
2547 -- 2554Alessandro Mammana, Martin Vingron, Ho-Ryun Chung. Inferring nucleosome positions with their histone mark annotation from ChIP data
2555 -- 2563Christopher Minas, Edward Curry, Giovanni Montana. A distance-based test of association between paired heterogeneous genomic data
2564 -- 2571Sarah Sheppard, Nathan D. Lawson, Lihua Julie Zhu. Accurate identification of polyadenylation sites from 3′ end deep sequencing using a naïve Bayes classifier
2572 -- 2578Sebastian Deorowicz, Agnieszka Danek, Szymon Grabowski. Genome compression: a novel approach for large collections
2579 -- 2587Jing Yang, Richard Jang, Yang Zhang, Hong-bin Shen. High-accuracy prediction of transmembrane inter-helix contacts and application to GPCR 3D structure modeling
2588 -- 2595Jianyi Yang, Ambrish Roy, Yang Zhang. Protein-ligand binding site recognition using complementary binding-specific substructure comparison and sequence profile alignment
2596 -- 2602Wei Jiang, Yan Zhang, Fanlin Meng, Baofeng Lian, Xiaowen Chen, Xuexin Yu, Enyu Dai, Shuyuan Wang, Xinyi Liu, Xiang Li, Lihong Wang, Xia Li. Identification of active transcription factor and miRNA regulatory pathways in Alzheimer's disease
2603 -- 2609Robert Maier, Ralf Zimmer, Robert Küffner. A Turing test for artificial expression data
2610 -- 2616Eric F. Lock, David B. Dunson. Bayesian consensus clustering
2617 -- 2624Xing Chen, Guiying Yan. Novel human lncRNA-disease association inference based on lncRNA expression profiles
2625 -- 2632Alberto Giovanni Busetto, Alain Hauser, Gabriel Krummenacher, Mikael Sunnåker, Sotiris Dimopoulos, Cheng Soon Ong, Jörg Stelling, Joachim M. Buhmann. Near-optimal experimental design for model selection in systems biology
2633 -- 2640Zixing Wang, Wenlong Xu, F. Anthony San Lucas, Yin Liu. Incorporating prior knowledge into Gene Network Study
2641 -- 2642Darren Curtis, Aaron Phillips, Stephen J. Callister, Sean Conlan, Lee Ann McCue. SPOCS: software for predicting and visualizing orthology/paralogy relationships among genomes
2643 -- 2644Alexis Allot, Yannick-Noël Anno, Laetitia Poidevin, Raymond Ripp, Olivier Poch, Odile Lecompte. PARSEC: PAtteRn SEarch and Contextualization
2645 -- 2646Jianghan Qu, Meng Zhou, Qiang Song, Elizabeth E. Hong, Andrew D. Smith. MLML: consistent simultaneous estimates of DNA methylation and hydroxymethylation
2647 -- 2648Wenlin Li, Lisa N. Kinch, Nick V. Grishin. Pclust: protein network visualization highlighting experimental data
2649 -- 2650Tomás Norambuena, Jorge F. Cares, Emidio Capriotti, Francisco Melo. WebRASP: a server for computing energy scores to assess the accuracy and stability of RNA 3D structures
2651 -- 2652Sören Müller, Lukas Rycak, Peter Winter, Günter Kahl, Ina Koch, Björn Rotter. omiRas: a Web server for differential expression analysis of miRNAs derived from small RNA-Seq data
2653 -- 2654Youyi Fong, Krisztian Sebestyen, XueSong Yu, Peter Gilbert, Steve Self. nCal: an R package for non-linear calibration
2655 -- 2656Matt K. Matlock, Jed Zaretzki, S. Joshua Swamidass. Scaffold network generator: a tool for mining molecular structures
2657 -- 2658Ganiraju Manyam, Cristina Ivan, George A. Calin, Kevin R. Coombes. targetHub: a programmable interface for miRNA-gene interactions
2659 -- 2660Igor Rodchenkov, Emek Demir, Chris Sander, Gary D. Bader. The BioPAX Validator
2661 -- 2663Paola Masuzzo, Niels Hulstaert, Lynn Huyck, Christophe Ampe, Marleen Van Troys, Lennart Martens. CellMissy: a tool for management, storage and analysis of cell migration data produced in wound healing-like assays
2664 -- 2666Anne-Laure Boulesteix. et al.
2667 -- 2668Attila Gyenesei, Colin A. M. Semple, Chris S. Haley, Wenhua Wei. Corrigendum of 'High throughput analysis of epistasis in genome-wide association studies with BiForce'

Volume 29, Issue 2

149 -- 159Wenting Wang, Veerabhadran Baladandayuthapani, Jeffrey S. Morris, Bradley M. Broom, Ganiraju Manyam, Kim-Anh Do. iBAG: integrative Bayesian analysis of high-dimensional multiplatform genomics data
160 -- 165Yang I. Li, Richard R. Copley. Scaffolding low quality genomes using orthologous protein sequences
166 -- 174Saad I. Sheikh, Tamer Kahveci, Sanjay Ranka, J. Gordon Burleigh. Stability analysis of phylogenetic trees
175 -- 181Ivan K. Huang, Jimin Pei, Nick V. Grishin. Defining and predicting structurally conserved regions in protein superfamilies
182 -- 188Mehmet Kocak, E. Olusegun George, Saumyadipta Pyne, Stanley Pounds. An empirical Bayes approach for analysis of diverse periodic trends in time-course gene expression data
189 -- 196Andrew E. Teschendorff, Francesco Marabita, Matthias Lechner, Thomas Bartlett, Jesper Tegnér, David Gomez-Cabrero, Stephan Beck. A beta-mixture quantile normalization method for correcting probe design bias in Illumina Infinium 450 k DNA methylation data
197 -- 205Mark Silberstein, Omer Weissbrod, Lars Otten, Anna Tzemach, Andrei Anisenia, Oren Shtark, Dvir Tuberg, Eddie Galfrin, Irena Gannon, Adel Shalata, Zvi U. Borochowitz, Rina Dechter, Elizabeth Thompson, Dan Geiger. A system for exact and approximate genetic linkage analysis of SNP data in large pedigrees
206 -- 214Barbara Rakitsch, Christoph Lippert, Oliver Stegle, Karsten M. Borgwardt. A Lasso multi-marker mixed model for association mapping with population structure correction
215 -- 222Richard Röttger, Prabhav Kalaghatgi, Peng Sun, Siomar de Castro Soares, Vasco Azevedo, Tobias Wittkop, Jan Baumbach. Density parameter estimation for finding clusters of homologous proteins - tracing actinobacterial pathogenicity lifestyles
223 -- 229Thomas Sütterlin, Christoph Kolb, Hartmut Dickhaus, Dirk Jäger, Niels Grabe. Bridging the scales: semantic integration of quantitative SBML in graphical multi-cellular models and simulations with EPISIM and COPASI
230 -- 237Li C. Xia, Dongmei Ai, Jacob Cram, Jed A. Fuhrman, Fengzhu Sun. Efficient statistical significance approximation for local similarity analysis of high-throughput time series data
238 -- 245Jian-Ping Mei, Chee Keong Kwoh, Peng Yang, Xiaoli Li, Jie Zheng. Drug-target interaction prediction by learning from local information and neighbors
246 -- 254Robert J. Flassig, S. Heise, Kai Sundmacher, Steffen Klamt. An effective framework for reconstructing gene regulatory networks from genetical genomics data
255 -- 261Frida Belinky, Iris Bahir, Gil Stelzer, Shahar Zimmerman, Naomi Rosen, Noam Nativ, Irina Dalah, Tsippi Iny Stein, Noa Rappaport, Toutai Mituyama, Marilyn Safran, Doron Lancet. Non-redundant compendium of human ncRNA genes in GeneCards
262 -- 263Jenna L. Butler, Marjorie Elizabeth Osborne Locke, Kathleen A. Hill, Mark Daley. HD-CNV: hotspot detector for copy number variants
264 -- 265David R. Powell, Torsten Seemann. VAGUE: a graphical user interface for the Velvet assembler
266 -- 267Yunxin Chen, Hui Yao, Erika J. Thompson, Nizar M. Tannir, John N. Weinstein, Xiaoping Su. VirusSeq: software to identify viruses and their integration sites using next-generation sequencing of human cancer tissue
268 -- 270Davide Campagna, Andrea Telatin, Claudio Forcato, Nicola Vitulo, Giorgio Valle. PASS-bis: a bisulfite aligner suitable for whole methylome analysis of Illumina and SOLiD reads
271 -- 272Michael Golden, Darren Martin. DOOSS: a tool for visual analysis of data overlaid on secondary structures
273 -- 274Dmitri D. Pervouchine, David G. Knowles, Roderic Guigó. Intron-centric estimation of alternative splicing from RNA-seq data
275 -- 276Zamin Iqbal, Isaac Turner, Gil McVean. High-throughput microbial population genomics using the Cortex variation assembler
277 -- 278Gerd Zschaler, Thilo Gross. Largenet2: an object-oriented programming library for simulating large adaptive networks
279 -- 280Guomin Ren, Zhihua Liu. NetCAD: a network analysis tool for coronary artery disease-associated PPI network
281 -- 283Achuthanunni Chokkathukalam, Andris Jankevics, Darren J. Creek, Fiona Achcar, Michael P. Barrett, Rainer Breitling. mzMatch-ISO: an R tool for the annotation and relative quantification of isotope-labelled mass spectrometry data
284 -- 285Alexandre P. Blanchard, Graeme S. V. McDowell, Nico Valenzuela, Hongbin Xu, Sarah Gelbard, Martin Bertrand, Gary W. Slater, Daniel Figeys, Stephen Fai, Steffany A. L. Bennett. Visualization and Phospholipid Identification (VaLID): online integrated search engine capable of identifying and visualizing glycerophospholipids with given mass
286 -- 289Ola Spjuth, Valentin Georgiev, Lars Carlsson, Jonathan Alvarsson, Arvid Berg, Egon L. Willighagen, Jarl E. S. Wikberg, Martin Eklund. Bioclipse-R: integrating management and visualization of life science data with statistical analysis
290 -- 291Nozomu Sakurai, Takeshi Ara, Shigehiko Kanaya, Yukiko Nakamura, Yoko Iijima, Mitsuo Enomoto, Takeshi Motegi, Koh Aoki, Hideyuki Suzuki, Daisuke Shibata. An application of a relational database system for high-throughput prediction of elemental compositions from accurate mass values
292 -- 294Jiayu Gong, Xiaofeng Liu, Xianwen Cao, Yanyan Diao, Daqi Gao, Honglin Li, Xuhong Qian. PTID: an integrated web resource and computational tool for agrochemical discovery
295 -- 297Yaping Fang, Hui-Xin Liu, Ning Zhang, Grace L. Guo, Yu-Jui Yvonne Wan, Jianwen Fang. NURBS: a database of experimental and predicted nuclear receptor binding sites of mouse
298 -- 0Tobias Pietzsch, Stephan Preibisch, Pavel Tomancak, Stephan Saalfeld. ImgLib2 - generic image processing in Java

Volume 29, Issue 19

2371 -- 2374Luis Sánchez-Pulido, Chris P. Ponting. Tiki, at the head of a new superfamily of enzymes
2375 -- 2379Zhenpeng Li, Xiuliang Cui, Fei Li, Peng Li, Ming Ni, Shengqi Wang, Xiaochen Bo. Exploring the role of human miRNAs in virus-host interactions using systematic overlap analysis
2380 -- 2386Robert Schöpflin, Vladimir B. Teif, Oliver Müller, Christin Weinberg, Karsten Rippe, Gero Wedemann. Modeling nucleosome position distributions from experimental nucleosome positioning maps
2387 -- 2394Jonathan M. Goldberg, Allison D. Griggs, Janet L. Smith, Brian J. Haas, Jennifer R. Wortman, Qiandong Zeng. Kinannote, a computer program to identify and classify members of the eukaryotic protein kinase superfamily
2395 -- 2401Zeinab Taghavi, Narjes S. Movahedi, Sorin Draghici, Hamidreza Chitsaz. de novo assembly for sparse microbial communities
2402 -- 2409Wenjie Deng, Brandon Maust, Dylan H. Westfall, Lennie Chen, Hong Zhao, Brendan B. Larsen, Shyamala Iyer, Yi Liu, James I. Mullins. Indel and Carryforward Correction (ICC): a new analysis approach for processing 454 pyrosequencing data
2410 -- 2418Amina Noor, Aitzaz Ahmad, Erchin Serpedin, Mohamed N. Nounou, Hazem N. Nounou. ROBNCA: robust network component analysis for recovering transcription factor activities
2419 -- 2426Manuel A. Rivas, Matti Pirinen, Matthew J. Neville, Kyle J. Gaulton, Loukas Moutsianas, Cecilia M. Lindgren, Fredrik Karpe, Mark I. McCarthy, Peter Donnelly. Assessing association between protein truncating variants and quantitative traits
2427 -- 2434Kui Zhang, Degui Zhi. Joint haplotype phasing and genotype calling of multiple individuals using haplotype informative reads
2435 -- 2444Wei-Ming Chen, Samuel A. Danziger, Jung-Hsien Chiang, John D. Aitchison. PhosphoChain: a novel algorithm to predict kinase and phosphatase networks from high-throughput expression data
2445 -- 2451Robert Smith, Tamil S. Anthonymuthu, Dan Ventura, John T. Prince. Statistical agglomeration: peak summarization for direct infusion lipidomics
2452 -- 2459Nikolas Kessler, Heiko Neuweger, Anja Bonte, Georg Langenkämper, Karsten Niehaus, Tim W. Nattkemper, Alexander Goesmann. MeltDB 2.0-advances of the metabolomics software system
2460 -- 2468V. Abrishami, A. Zaldívar-Peraza, J. M. de la Rosa-Trevín, J. Vargas, Joaquín Otón, Roberto Marabini, Yoel Shkolnisky, José María Carazo, Carlos Oscar Sánchez Sorzano. A pattern matching approach to the automatic selection of particles from low-contrast electron micrographs
2469 -- 2476Jijie Wang, Henry Lam. Graph-based peak alignment algorithms for multiple liquid chromatography-mass spectrometry datasets
2477 -- 2478Simon J. McGowan, Jim R. Hughes, Zong-Pei Han, Stephen Taylor. MIG: Multi-Image Genome viewer
2479 -- 2481Daniel Jost. Twist-DNA: computing base-pair and bubble opening probabilities in genomic superhelical DNA
2482 -- 2484Christopher Yau. OncoSNP-SEQ: a statistical approach for the identification of somatic copy number alterations from next-generation sequencing of cancer genomes
2485 -- 2486Alper Küçükural, Hakan Özadam, Guramrit Singh, Melissa J. Moore, Can Cenik. ASPeak: an abundance sensitive peak detection algorithm for RIP-Seq
2487 -- 2489Travis J. Wheeler, Sean R. Eddy. nhmmer: DNA homology search with profile HMMs
2490 -- 2493Lucian Ilie, Michael Molnar. RACER: Rapid and accurate correction of errors in reads
2494 -- 2495Matija Korpar, Mile Sikic. SW#-GPU-enabled exact alignments on genome scale
2496 -- 2497Josef Maier, Alexei A. Adzhubei, Wolfgang Egge-Jacobsen. SAPA tool: finding protein regions by combination of amino acid composition, scaled profiles, patterns and rules
2498 -- 2500Chiao-Feng Lin, Otto Valladares, Daniel M. Childress, Egor Klevak, Evan T. Geller, Yih-Chii Hwang, Ellen A. Tsai, Gerard D. Schellenberg, Li-San Wang. DRAW+SneakPeek: Analysis workflow and quality metric management for DNA-seq experiments
2501 -- 2502Diana H. P. Low, Efthymios Motakis. deltaGseg: macrostate estimation via molecular dynamics simulations and multiscale time series analysis
2503 -- 2504Andreas Spitz, Katharina A. Zweig, Emoke-Ágnes Horvát. SICOP: identifying significant co-interaction patterns
2505 -- 2506Esther Camilo, Luiz A. Bovolenta, Marcio L. Acencio, José L. Rybarczyk Filho, Mauro A. A. Castro, José C. F. Moreira, Ney Lemke. GALANT: a Cytoscape plugin for visualizing data as functional landscapes projected onto biological networks
2507 -- 2508Jennifer E. Dent, Xinyi Yang, Christine Nardini. SPNConverter: a new link between static and dynamic complex network analysis
2509 -- 2511Quanwei Zhang, Zhengdong D. Zhang. SubNet: a Java application for subnetwork extraction
2512 -- 2514Alexander Miguel Monzon, Ezequiel I. Juritz, María Silvina Fornasari, Gustavo D. Parisi. CoDNaS: a database of conformational diversity in the native state of proteins
2515 -- 2516Mohd Danishuddin, Mohd Hassan Baig, Lalima Kaushal, Asad U. Khan. BLAD: A comprehensive database of widely circulated beta-lactamases
2517 -- 2518Foivos Gypas, Georgios N. Tsaousis, Stavros J. Hamodrakas. mpMoRFsDB: a database of molecular recognition features in membrane proteins
2519 -- 2520Konika Chawla, Sushil Tripathi, Liv Thommesen, Astrid Lægreid, Martin Kuiper. TFcheckpoint: a curated compendium of specific DNA-binding RNA polymerase II transcription factors

Volume 29, Issue 18

2223 -- 2230Nicola D. Roberts, R. Daniel Kortschak, Wendy T. Parker, Andreas W. Schreiber, Susan Branford, Hamish S. Scott, Garique Glonek, David L. Adelson. A comparative analysis of algorithms for somatic SNV detection in cancer
2231 -- 2237William K. M. Lai, Michael J. Buck. An integrative approach to understanding the combinatorial histone code at functional elements
2238 -- 2244David Tamborero, Abel Gonzalez-Perez, Nuria Lopez-Bigas. OncodriveCLUST: exploiting the positional clustering of somatic mutations to identify cancer genes
2245 -- 2252Wen-Yun Yang, Farhad Hormozdiari, Zhanyong Wang, Dan He, Bogdan Pasaniuc, Eleazar Eskin. Leveraging reads that span multiple single nucleotide polymorphisms for haplotype inference from sequencing data
2253 -- 2260Sasha Ames, David A. Hysom, Shea N. Gardner, G. Scott Lloyd, Maya B. Gokhale, Jonathan E. Allen. Scalable metagenomic taxonomy classification using a reference genome database
2261 -- 2268Qin Ma, Bingqiang Liu, Chuan Zhou, Yanbin Yin, Guojun Li, Ying Xu. cis-regulatory motifs at a genome scale
2269 -- 2276Juan Wang, Maozu Guo, Xiaoyan Liu, Yang Liu, Chun-yu Wang, Linlin Xing, Kai Che. Lnetwork: an efficient and effective method for constructing phylogenetic networks
2277 -- 2284Md. Shamsuzzoha Bayzid, Tandy Warnow. Naive binning improves phylogenomic analyses
2285 -- 2291Pier Paolo Olimpieri, Anna Chailyan, Anna Tramontano, Paolo Marcatili. Prediction of site-specific interactions in antibody-antigen complexes: the proABC method and server
2292 -- 2299Naoki Nariai, Osamu Hirose, Kaname Kojima, Masao Nagasaki. TIGAR: transcript isoform abundance estimation method with gapped alignment of RNA-Seq data by variational Bayesian inference
2300 -- 2310Laura H. LeGault, Colin N. Dewey. Inference of alternative splicing from RNA-Seq data with probabilistic splice graphs
2311 -- 2319Gabriele Lillacci, Mustafa Khammash. The signal within the noise: efficient inference of stochastic gene regulation models using fluorescence histograms and stochastic simulations
2320 -- 2326Carito Guziolowski, Santiago Videla, Federica Eduati, Sven Thiele, Thomas Cokelaer, Anne Siegel, Julio Saez-Rodriguez. Exhaustively characterizing feasible logic models of a signaling network using Answer Set Programming
2327 -- 2334Elisenda Feliu, Carsten Wiuf. A computational method to preclude multistationarity in networks of interacting species
2335 -- 2342Theodore Alexandrov, Andreas Bartels. Testing for presence of known and unknown molecules in imaging mass spectrometry
2343 -- 2349Luís Pedro Coelho, Joshua Kangas, Armaghan W. Naik, Elvira Osuna-Highley, Estelle Glory-Afshar, Margaret Fuhrman, Ramanuja Simha, Peter B. Berget, Jonathan W. Jarvik, Robert F. Murphy. Determining the subcellular location of new proteins from microscope images using local features
2350 -- 2352Joanna L. Sharman, Dietlind L. Gerloff. MaGnET: Malaria Genome Exploration Tool
2353 -- 2354Susan K. Rathe, James E. Johnson, Kevin A. T. Silverstein, Jesse J. Erdmann, Adrienne L. Watson, Flavia E. Popescu, John R. Ohlfest, David A. Largaespada. MMuFLR: missense mutation and frameshift location reporter
2355 -- 2356Hernán F. Morales, Guillermo Giovambattista. BioSmalltalk: a pure object system and library for bioinformatics
2357 -- 2359Wenkang Huang, Shaoyong Lu, Zhimin Huang, Xinyi Liu, Linkai Mou, Yu Luo, Yanlong Zhao, Yaqin Liu, Zhongjie Chen, Tingjun Hou, Jian Zhang. Allosite: a method for predicting allosteric sites
2360 -- 2362Joan Planas-Iglesias, Manuel A. Marin-Lopez, Jaume Bonet, Javier Garcia-Garcia, Baldo Oliva. iLoops: a protein-protein interaction prediction server based on structural features
2363 -- 2364Víctor A. Gil, Victor Guallar. pyRMSD: a Python package for efficient pairwise RMSD matrix calculation and handling
2365 -- 2368Nicolas De Jay, Simon Papillon-Cavanagh, Catharina Olsen, Nehme Hachem, Gianluca Bontempi, Benjamin Haibe-Kains. mRMRe: an R package for parallelized mRMR ensemble feature selection
2369 -- 2370Wesley Schaal, Ulf Hammerling, Mats G. Gustafsson, Ola Spjuth. Automated QuantMap for rapid quantitative molecular network topology analysis

Volume 29, Issue 17

2075 -- 2083Julie Nocq, Magalie Celton, Patrick Gendron, Sébastien Lemieux, Brian T. Wilhelm. Harnessing virtual machines to simplify next-generation DNA sequencing analysis
2084 -- 2087Mikita Suyama. dynamin 1
2088 -- 2095Stan Pounds, Cheng Cheng, Shaoyu Li, Zhifa Liu, Jinghui Zhang, Charles Mullighan. A genomic random interval model for statistical analysis of genomic lesion data
2096 -- 2102David Koslicki, Simon Foucart, Gail Rosen. Quikr: a method for rapid reconstruction of bacterial communities via compressive sensing
2103 -- 2111Yuan Zhang, Yanni Sun, James R. Cole. A Sensitive and Accurate protein domain cLassification Tool (SALT) for short reads
2112 -- 2121Francisco M. Ortuño Guzman, Olga Valenzuela, Fernando Rojas, Héctor Pomares, Javier P. Florido, José M. Urquiza, Ignacio Rojas. Optimizing multiple sequence alignments using a genetic algorithm based on three objectives: structural information, non-gaps percentage and totally conserved columns
2122 -- 2128Joanna S. G. Slusky, Roland L. Dunbrack Jr.. Charge asymmetry in the proteins of the outer membrane
2129 -- 2136Seydou Traoré, David Allouche, Isabelle André, Simon de Givry, George Katsirelos, Thomas Schiex, Sophie Barbe. A new framework for computational protein design through cost function network optimization
2137 -- 2145Xiaowei Chen, Frank J. Slack, Hongyu Zhao. Joint analysis of expression profiles from multiple cancers improves the identification of microRNA-gene interactions
2146 -- 2152Andrea Rau, Mélina Gallopin, Gilles Celeux, Florence Jaffrézic. Data-based filtering for replicated high-throughput transcriptome sequencing experiments
2153 -- 2161Ei-Wen Yang, Thomas Girke, Tao Jiang. Differential gene expression analysis using coexpression and RNA-Seq data
2162 -- 2168Yuju Lee, Qing Zhou. Co-regulation in embryonic stem cells via context-dependent binding of transcription factors
2169 -- 2177Wei Liu, Chunquan Li, Yanjun Xu, Haixiu Yang, Qianlan Yao, Junwei Han, Desi Shang, Chunlong Zhang, Fei Su, Xiaoxi Li, Yun Xiao, Fan Zhang, Meng Dai, Xia Li. Topologically inferring risk-active pathways toward precise cancer classification by directed random walk
2178 -- 2185Yang Zhao, Takeyuki Tamura, Tatsuya Akutsu, Jean-Philippe Vert. Flux balance impact degree: a new definition of impact degree to properly treat reversible reactions in metabolic networks
2186 -- 2194Rong Xu, Li Li, QuanQiu Wang. Towards building a disease-phenotype knowledge base: extracting disease-manifestation relationship from literature
2195 -- 2196René Snajder, Zlatko Trajanoski, Hubert Hackl. GPViz: dynamic visualization of genomic regions and variants affecting protein domains
2197 -- 2198Maxim Barenboim, Thomas Manke. ChroMoS: an integrated web tool for SNP classification, prioritization and functional interpretation
2199 -- 2202Dmitri S. Pavlichin, Tsachy Weissman, Golan Yona. The human genome contracts again
2203 -- 2205Martin Triska, David Grocutt, James Southern, Denis J. Murphy, Tatiana Tatarinova. cisExpress: motif detection in DNA sequences
2206 -- 2207Ryo Sakai, Matthieu Moisse, Joke Reumers, Jan Aerts. Pipit: visualizing functional impacts of structural variations
2208 -- 2210Mamunur Rashid, Carla Daniela Robles-Espinoza, Alistair G. Rust, David J. Adams. Cake: a bioinformatics pipeline for the integrated analysis of somatic variants in cancer genomes
2211 -- 2212Renaud Gaujoux, Cathal Seoighe. CellMix: a comprehensive toolbox for gene expression deconvolution
2213 -- 2215John W. May, A. Gordon James, Christoph Steinbeck. Metingear: a development environment for annotating genome-scale metabolic models
2216 -- 2217Sebastian Vlaic, Bianca Hoffmann, Peter Kupfer, Michael Weber, Andreas Dräger. GRN2SBML: automated encoding and annotation of inferred gene regulatory networks complying with SBML
2218 -- 2220Rui Zhong, Min-Soo Kim, Michael A. White, Yang Xie, Guanghua Xiao. SbacHTS: Spatial background noise correction for High-Throughput RNAi Screening
2221 -- 2222Ke Liu, Zhangming Yan, Yuchao Li, Zhirong Sun. Linc2GO: a human LincRNA function annotation resource based on ceRNA hypothesis

Volume 29, Issue 16

1925 -- 1933Benjamin M. Good, Andrew I. Su. Crowdsourcing for bioinformatics
1934 -- 1937Aurelio A. Moya-García, Juan A. G. Ranea. Insights into polypharmacology from drug-domain associations
1938 -- 1945Zhi-Zhong Chen, Fei Deng, Lusheng Wang. Exact algorithms for haplotype assembly from whole-genome sequence data
1946 -- 1952Dominik Heider, Robin Senge, Weiwei Cheng, Eyke Hüllermeier. Multilabel classification for exploiting cross-resistance information in HIV-1 drug resistance prediction
1953 -- 1962Kyowon Jeong, Sangtae Kim, Pavel A. Pevzner. de novo peptide sequencing
1963 -- 1969Jérôme Ambroise, Anne-Sophie Piette, Cathy Delcorps, Leen Rigouts, Bouke C. de Jong, Leonid Irenge, Annie Robert, Jean-Luc Gala. AdvISER-PYRO: Amplicon Identification using SparsE Representation of PYROsequencing signal
1970 -- 1979Guy Baele, Philippe Lemey. Bayesian evolutionary model testing in the phylogenomics era: matching model complexity with computational efficiency
1980 -- 1986Pedro Sfriso, Adam Hospital, Agustí Emperador, Modesto Orozco. Exploration of conformational transition pathways from coarse-grained simulations
1987 -- 1996Shandian Zhe, Syed A. Z. Naqvi, Yifan Yang, Yuan Qi. Joint network and node selection for pathway-based genomic data analysis
1997 -- 2003Colin D. Veal, Hang Xu, Katherine Reekie, Robert C. Free, Robert J. Hardwick, David McVey, Anthony J. Brookes, Edward J. Hollox, Christopher J. Talbot. Automated design of paralogue ratio test assays for the accurate and rapid typing of copy number variation
2004 -- 2008Salvatore Alaimo, Alfredo Pulvirenti, Rosalba Giugno, Alfredo Ferro. Drug-target interaction prediction through domain-tuned network-based inference
2009 -- 2016Alberto Rezola, Jon Pey, Luis F. de Figueiredo, Adam Podhorski, Stefan Schuster, Angel Rubio, Francisco J. Planes. Selection of human tissue-specific elementary flux modes using gene expression data
2017 -- 2023Jinmyung Jung, Doheon Lee. Inferring disease association using clinical factors in a combinatorial manner and their use in drug repositioning
2024 -- 2031Xi Zhou, Pengcheng Chen, Qiang Wei, Xueling Shen, Xin Chen. Human interactome resource and gene set linkage analysis for the functional interpretation of biologically meaningful gene sets
2032 -- 2040Ying-Ying Xu, Fan Yang, Yang Zhang, Hong-bin Shen. iLocator) reveals protein mislocalizations in cancer tissues
2041 -- 2043Come Raczy, Roman Petrovski, Christopher T. Saunders, Ilya Chorny, Semyon Kruglyak, Elliott H. Margulies, Han-Yu Chuang, Morten Källberg, Swathi A. Kumar, Arnold Liao, Kristina M. Little, Michael P. Strömberg, Stephen W. Tanner. Isaac: ultra-fast whole-genome secondary analysis on Illumina sequencing platforms
2044 -- 2045Jianlin He, Xinxi Sun, Xiaojian Shao, Liji Liang, Hehuang Xie. DMEAS: DNA methylation entropy analysis software
2046 -- 2048Andreas Heger, Caleb Webber, Martin Goodson, Chris P. Ponting, Gerton Lunter. GAT: a simulation framework for testing the association of genomic intervals
2049 -- 2050Sangsoon Woo, Xuekui Zhang, Renan Sauteraud, François Robert, Raphael Gottardo. PING 2.0: an R/Bioconductor package for nucleosome positioning using next-generation sequencing data
2051 -- 2052Michal Rostkowski, Ola Spjuth, Patrik Rydberg. WhichCyp: prediction of cytochromes P450 inhibition
2053 -- 2055Alessandro Pandini, Arianna Fornili, Franca Fraternali, Jens Kleinjung. GSATools: analysis of allosteric communication and functional local motions using a structural alphabet
2056 -- 2058Claudio Mirabello, Gianluca Pollastri. Porter, PaleAle 4.0: high-accuracy prediction of protein secondary structure and relative solvent accessibility
2059 -- 2061Inna Dubchak, Matthew Munoz, Alexander Poliakov, Nathan Salomonis, Simon Minovitsky, Rolf Bodmer, Alexander C. Zambon. Whole-Genome rVISTA: a tool to determine enrichment of transcription factor binding sites in gene promoters from transcriptomic data
2062 -- 2063Alexey Lagunin, Sergey Ivanov, Anastasia Rudik, Dmitry Filimonov, Vladimir Poroikov. in silico prediction of drug-induced gene expression profiles based on structural formula
2064 -- 2065Yingfeng Wang, Tae-Hyuk Ahn, Zhou Li, Chongle Pan. Sipros/ProRata: a versatile informatics system for quantitative community proteomics
2066 -- 2067Chao Zhang, Jiguang Wang, Kristina Hanspers, Dong Xu, Luonan Chen, Alexander R. Pico. NOA: a cytoscape plugin for network ontology analysis
2068 -- 2070Norbert Dojer, Pawel Bednarz, Agnieszka Podsiadlo, Bartek Wilczynski. BNFinder2: Faster Bayesian network learning and Bayesian classification
2071 -- 2072Bülent Arman Aksoy, Jianjiong Gao, Gideon Dresdner, Weiqing Wang, Alex Root, Xiaohong Jing, Ethan G. Cerami, Chris Sander. PiHelper: an open source framework for drug-target and antibody-target data
2073 -- 0Ning Leng, John A. Dawson, James A. Thomson, Victor Ruotti, Anna I. Rissman, Bart M. G. Smits, Jill D. Haag, Michael N. Gould, Ron M. Stewart, Christina Kendziorski. EBSeq: an empirical Bayes hierarchical model for inference in RNA-seq experiments

Volume 29, Issue 15

1843 -- 1850Orion J. Buske, AshokKumar Manickaraj, Seema Mital, Peter N. Ray, Michael Brudno. Identification of deleterious synonymous variants in human genomes
1851 -- 1857Paul Geeleher, Lori Hartnett, Laurance J. Egan, Aaron Golden, Raja Affendi Raja Ali, Cathal Seoighe. Gene-set analysis is severely biased when applied to genome-wide methylation data
1858 -- 1864Michael S. Porter, Robert G. Beiko. SPANNER: taxonomic assignment of sequences using pyramid matching of similarity profiles
1865 -- 1871Jaeil Ahn, Ying Yuan, Giovanni Parmigiani, Milind B. Suraokar, Lixia Diao, Ignacio I. Wistuba, Wenyi Wang. DeMix: deconvolution for mixed cancer transcriptomes using raw measured data
1872 -- 1878Christopher M. Tan, Edward Y. Chen, Ruth Dannenfelser, Neil R. Clark, Avi Ma'ayan. Network2Canvas: network visualization on a canvas with enrichment analysis
1879 -- 1887Ching-Wei Wang, Hsiang-Chou Chen. Improved image alignment method in application to X-ray images and biological images
1888 -- 1889Nicholas B. Larson, Brooke L. Fridley. PurBayes: estimating tumor cellularity and subclonality in next-generation sequencing data
1890 -- 1892Graham J. Etherington, Daniel MacLean. SVGenes: a library for rendering genomic features in scalable vector graphic format
1893 -- 1894Alexei Nordell Markovits, Charles Joly Beauparlant, Dominique Toupin, Shengrui Wang, Arnaud Droit, Nicolas Gevry. NGS++: a library for rapid prototyping of epigenomics software tools
1895 -- 1897Fabian A. Buske, Denis C. Bauer, John S. Mattick, Timothy L. Bailey. Triplex-Inspector: an analysis tool for triplex-mediated targeting of genomic loci
1898 -- 1899Ka-Kyung Kim, Juyoung Ham, Sung Wook Chi. miRTCat: a comprehensive map of human and mouse microRNA target sites including non-canonical nucleation bulges
1900 -- 1901Jirí Hon, Tomás Martínek, Kamil Rajdl, Matej Lexa. Triplex: an R/Bioconductor package for identification and visualization of potential intramolecular triplex patterns in DNA sequences
1902 -- 1903Mick Watson, Esther Schnettler, Alain Kohl. viRome: an R package for the visualization and analysis of viral small RNA sequence datasets
1904 -- 1907Varun Jaiswal, Sree K. Chanumolu, Pankaj Sharma, Rajinder S. Chauhan, Chittaranjan Rout. EpiCombFlu: exploring known influenza epitopes and their combination to design a universal influenza vaccine
1908 -- 1909Shawn E. Yost, Hakan Alakus, Hiroko Matsui, Richard B. Schwab, Kristen Jepsen, Kelly A. Frazer, Olivier Harismendy. Mutascope: sensitive detection of somatic mutations from deep amplicon sequencing
1910 -- 1912Xueping Liu, Ingo Vogt, Tanzeem Haque, Mónica Campillos. HitPick: a web server for hit identification and target prediction of chemical screenings
1913 -- 1914Eduardo P. Costa, Gerben Menschaert, Walter Luyten, Kurt De Grave, Jan Ramon. PIUS: peptide identification by unbiased search
1915 -- 1916Tiago Nunes, David Campos, Sérgio Matos, José Luís Oliveira. BeCAS: biomedical concept recognition services and visualization
1917 -- 1918Jindan Zhou, Andrew J. Richardson, Kenneth E. Rudd. EcoGene-RefSeq: EcoGene tools applied to the RefSeq prokaryotic genomes
1919 -- 1921Rafael C. Jimenez, Juan P. Albar, Jong Bhak, Marie-Claude Blatter, Thomas Blicher, Michelle D. Brazas, Catherine Brooksbank, Aidan Budd, Javier De Las Rivas, Jacqueline Dreyer, Marc A. van Driel, Michael J. Dunn, Pedro L. Fernandes, Celia W. G. van Gelder, Henning Hermjakob, Vassilios Ioannidis, David Phillip Judge, Pascal Kahlem, Eija Korpelainen, Hans-Joachim Kraus, Jane Loveland, Christine Mayer, Jennifer McDowall, Federico Moran, Nicola J. Mulder, Tommi H. Nyrönen, Kristian Rother, Gustavo A. Salazar, Reinhard Schneider 0002, Allegra Via, Jose M. Villaveces, Ping Yu, Maria Victoria Schneider, Teresa K. Attwood, Manuel Corpas. iAnn: an event sharing platform for the life sciences
1919 -- 1921Rafael C. Jimenez, Juan P. Albar, Jong Bhak, Marie-Claude Blatter, Thomas Blicher, Michelle D. Brazas, Catherine Brooksbank, Aidan Budd, Javier De Las Rivas, Jacqueline Dreyer, Marc A. van Driel, Michael J. Dunn, Pedro L. Fernandes, Celia W. G. van Gelder, Henning Hermjakob, Vassilios Ioannidis, David Phillip Judge, Pascal Kahlem, Eija Korpelainen, Hans-Joachim Kraus, Jane Loveland, Christine Mayer, Jennifer McDowall, Federico Moran, Nicola J. Mulder, Tommi H. Nyrönen, Kristian Rother, Gustavo A. Salazar, Reinhard Schneider 0002, Allegra Via, Jose M. Villaveces, Ping Yu, Maria Victoria Schneider, Teresa K. Attwood, Manuel Corpas. iAnn: an event sharing platform for the life sciences
1922 -- 1924Raymond K. Auerbach, Bin Chen, Atul J. Butte. Relating genes to function: identifying enriched transcription factors using the ENCODE ChIP-Seq significance tool

Volume 29, Issue 14

1713 -- 1717Che-Yu Lee, Liang Chen. Alternative polyadenylation sites reveal distinct chromatin accessibility and histone modification in human cell lines
1718 -- 1725Tanja Magoc, Stephan Pabinger, Stefan Canzar, Xinyue Liu, Qi Su, Daniela Puiu, Luke J. Tallon, Steven L. Salzberg. GAGE-B: an evaluation of genome assemblers for bacterial organisms
1726 -- 1733Guilhem Faure, Isabelle Callebaut. Identification of hidden relationships from the coupling of Hydrophobic Cluster Analysis and Domain Architecture information
1734 -- 1741Hongseok Tae, Kevin W. McMahon, Robert E. Settlage, Jasmin H. Bavarva, Harold R. Garner. ReviSTER: an automated pipeline to revise misaligned reads to simple tandem repeats
1742 -- 1749Jessica Andreani, Guilhem Faure, Raphaël Guérois. InterEvScore: a novel coarse-grained interface scoring function using a multi-body statistical potential coupled to evolution
1750 -- 1757Christoph Wiedemann, Peter Bellstedt, Matthias Görlach. CAPITO - a web server-based analysis and plotting tool for circular dichroism data
1758 -- 1767Mohammadmahdi R. Yousefi, Edward R. Dougherty. Intervention in gene regulatory networks with maximal phenotype alteration
1768 -- 1775Hao Lin, Lin He, Bin Ma. A combinatorial approach to the peptide feature matching problem for label-free quantification
1776 -- 1785Gennaro Gambardella, Maria Nicoletta Moretti, Rossella de Cegli, Luca Cardone, Adriano Peron, Diego di Bernardo. Differential network analysis for the identification of condition-specific pathway activity and regulation
1786 -- 1792Xiaoli Wei, Xue Shi, Imhoi Koo, Seongho Kim, Robin H. Schmidt, Gavin E. Arteel, Walter H. Watson, Craig McClain, Xiang Zhang. MetPP: a computational platform for comprehensive two-dimensional gas chromatography time-of-flight mass spectrometry-based metabolomics
1793 -- 1800Laura Tolosi, Jessica Theißen, Konstantin Halachev, Barbara Hero, Frank Berthold, Thomas Lengauer. A method for finding consensus breakpoints in the cancer genome from copy number data
1801 -- 1802Ryo Sakai, Alejandro Sifrim, Andrew Vande Moere, Jan Aerts. TrioVis: a visualization approach for filtering genomic variants of parent-child trios
1803 -- 1805Zheng-Zheng Tang, Dan-Yu Lin. MASS: meta-analysis of score statistics for sequencing studies
1806 -- 1808Masahiko Kumagai, Jungsok Kim, Ryutaro Itoh, Takeshi Itoh. Tasuke: a web-based visualization program for large-scale resequencing data
1809 -- 1810Michael Piechotta, Christoph Dieterich. ACCUSA2: multi-purpose SNV calling enhanced by probabilistic integration of quality scores
1811 -- 1812Daniel Lopez, Florencio Pazos. COPRED: prediction of fold, GO molecular function and functional residues at the domain level
1813 -- 1814Ernesto Picardi, Graziano Pesole. REDItools: high-throughput RNA editing detection made easy
1815 -- 1816Marcin J. Skwark, Abbi Abdel-Rehim, Arne Elofsson. PconsC: combination of direct information methods and alignments improves contact prediction
1817 -- 1818Marcin J. Skwark, Arne Elofsson. PconsD: ultra rapid, accurate model quality assessment for protein structure prediction
1819 -- 1820Adam Mazur, Björn Hammesfahr, Christian Griesinger, Donghan Lee, Martin Kollmar. ShereKhan - calculating exchange parameters in relaxation dispersion data from CPMG experiments
1821 -- 1822Rosalba Lepore, Anna Tramontano, Allegra Via. TiPs: a database of therapeutic targets in pathogens and associated tools
1823 -- 1824Lea A. I. Vaas, Johannes Sikorski, Benjamin Hofner, Anne Fiebig, Nora Buddruhs, Hans-Peter Klenk, Markus Göker. ® phenotype microarray data
1825 -- 1826Luca Beltrame, Luca Bianco, Paolo Fontana, Duccio Cavalieri. Pathway Processor 2.0: a web resource for pathway-based analysis of high-throughput data
1827 -- 1829Jiayu Gong, Chaoqian Cai, Xiaofeng Liu, Xin Ku, Hualiang Jiang, Daqi Gao, Honglin Li. ChemMapper: a versatile web server for exploring pharmacology and chemical structure association based on molecular 3D similarity method
1830 -- 1831Weijun Luo, Cory Brouwer. Pathview: an R/Bioconductor package for pathway-based data integration and visualization
1832 -- 1833Kun Yang, Ashok Reddy Dinasarapu, Edimara S. Reis, Robert A. DeAngelis, Daniel Ricklin, Shankar Subramaniam, John D. Lambris. CMAP: Complement Map Database
1834 -- 1836Changhe Fu, Guangxu Jin, Junfeng Gao, Rui Zhu, Efren Ballesteros-Villagrana, Stephen T. C. Wong. DrugMap Central: an on-line query and visualization tool to facilitate drug repositioning studies
1837 -- 1839Lin Dai, Ming Tian, Jiayan Wu, Jing-Fa Xiao, Xumin Wang, Jeffrey P. Townsend, Zhang Zhang. AuthorReward: increasing community curation in biological knowledge wikis through automated authorship quantification
1840 -- 1841Jean Ollion, Julien Cochennec, François Loll, Christophe Escudé, Thomas Boudier. TANGO: a generic tool for high-throughput 3D image analysis for studying nuclear organization

Volume 29, Issue 13

1 -- 2Nir Ben-Tal. Editorial
9 -- 17Saket Navlakha, Joseph Suhan, Alison L. Barth, Ziv Bar-Joseph. A high-throughput framework to detect synapses in electron microscopy images
18 -- 26Sarah J. Aerni, Xiao Liu, Chuong B. Do, Samuel S. Gross, Andy Nguyen, Stephen D. Guo, Fuhui Long, Hanchuan Peng, Stuart S. Kim, Serafim Batzoglou. Caenorhabditis elegans
27 -- 35Iulian Pruteanu-Malinici, William H. Majoros, Uwe Ohler. Automated annotation of gene expression image sequences via non-parametric factor analysis and conditional random fields
36 -- 43Noa Liscovitch, Uri Shalit, Gal Chechik. FuncISH: learning a functional representation of neural ISH images
44 -- 52Makoto Miwa, Tomoko Ohta, Rafal Rak, Andrew Rowley, Douglas B. Kell, Sampo Pyysalo, Sophia Ananiadou. A method for integrating and ranking the evidence for biochemical pathways by mining reactions from text
53 -- 61Wyatt T. Clark, Predrag Radivojac. Information-theoretic evaluation of predicted ontological annotations
62 -- 70Andrew J. Sedgewick, Stephen C. Benz, Shahrooz Rabizadeh, Patrick Soon-Shiong, Charles J. Vaske. Learning subgroup-specific regulatory interactions and regulator independence with PARADIGM
71 -- 79Yaron Orenstein, Ron Shamir. k-mers with applications to protein-binding microarrays and synthetic enhancers
80 -- 88Nicola Bonzanni, Abhishek Garg, K. Anton Feenstra, Judith Schütte, Sarah Kinston, Diego Miranda-Saavedra, Jaap Heringa, Ioannis Xenarios, Berthold Göttgens. Hard-wired heterogeneity in blood stem cells revealed using a dynamic regulatory network model
89 -- 97Hai-son Le, Ziv Bar-Joseph. Integrating sequence, expression and interaction data to determine condition-specific miRNA regulation
98 -- 107Hiroyuki Kuwahara, Ming Fan, Suojin Wang, Xin Gao. A framework for scalable parameter estimation of gene circuit models using structural information
108 -- 116Dina Hafez, Ting Ni, Sayan Mukherjee, Jun Zhu, Uwe Ohler. Genome-wide identification and predictive modeling of tissue-specific alternative polyadenylation
117 -- 125Fantine Mordelet, John Horton, Alexander J. Hartemink, Barbara E. Engelhardt, Raluca Gordân. Stability selection for regression-based models of transcription factor-DNA binding specificity
126 -- 134Yuhao Wang, Jianyang Zeng. Predicting drug-target interactions using restricted Boltzmann machines
135 -- 144Masaaki Kotera, Yasuo Tabei, Yoshihiro Yamanishi, Toshiaki Tokimatsu, Susumu Goto. de novo reconstruction of metabolic pathways from metabolome-scale compound sets
145 -- 153Gamze Abaka, Türker Bíyíkoglu, Cesim Erten. CAMPways: constrained alignment framework for the comparative analysis of a pair of metabolic pathways
154 -- 161Rodrigo Liberal, John W. Pinney. Simple topological properties predict functional misannotations in a metabolic network
162 -- 170Dan He. IBD-Groupon: an efficient method for detecting group-wise identity-by-descent regions simultaneously in multiple individuals based on pairwise IBD relationships
171 -- 179Chloé-Agathe Azencott, Dominik Grimm, Mahito Sugiyama, Yoshinobu Kawahara, Karsten M. Borgwardt. Efficient network-guided multi-locus association mapping with graph cuts
180 -- 188Pier Francesco Palamara, Itsik Pe'er. Inference of historical migration rates via haplotype sharing
189 -- 198Salim Akhter Chowdhury, Stanley Shackney, Kerstin Heselmeyer-Haddad, Thomas Ried, Alejandro A. Schäffer, Russell Schwartz. in situ hybridization data from tumor cell populations
199 -- 209Carlo Vittorio Cannistraci, Gregorio Alanis-Lobato, Timothy Ravasi. Minimum curvilinearity to enhance topological prediction of protein interactions by network embedding
210 -- 216Alexander Lan, Michal Ziv-Ukelson, Esti Yeger Lotem. A context-sensitive framework for the analysis of human signalling pathways in molecular interaction networks
217 -- 226Meghana Kshirsagar, Jaime G. Carbonell, Judith Klein-Seetharaman. Multitask learning for host-pathogen protein interactions
227 -- 236Anthony Gitter, Ziv Bar-Joseph. Identifying proteins controlling key disease signaling pathways
237 -- 246Robert Patro, Carl Kingsford. Predicting protein interactions via parsimonious network history inference
247 -- 256Zhidong Xue, Dong Xu, Yan Wang, Yang Zhang. ThreaDom: extracting protein domain boundary information from multiple threading alignments
257 -- 265Jianzhu Ma, Sheng Wang, Feng Zhao, Jinbo Xu. Protein threading using context-specific alignment potential
266 -- 273Zhiyong Wang, Jinbo Xu. Predicting protein contact map using evolutionary and physical constraints by integer programming
274 -- 282Min Xu, Frank Alber. Automated target segmentation and real space fast alignment methods for high-throughput classification and averaging of crowded cryo-electron subtomograms
283 -- 290Noah M. Daniels, Andrew Gallant, Jian Peng, Lenore J. Cowen, Michael Baym, Bonnie Berger. Compressive genomics for protein databases
291 -- 299Zhaojun Zhang, Shunping Huang, Jack Wang, Xiang Zhang, Fernando Pardo-Manuel de Villena, Leonard McMillan, Wei Wang 0010. GeneScissors: a comprehensive approach to detecting and correcting spurious transcriptome inference owing to RNA-seq reads misalignment
300 -- 307Elmirasadat Forouzmand, Hamidreza Chitsaz. The RNA Newton polytope and learnability of energy parameters
308 -- 315Vladimir Reinharz, Yann Ponty, Jérôme Waldispühl. A weighted sampling algorithm for the design of RNA sequences with targeted secondary structure and nucleotide distribution
316 -- 325Bo Xie, Boris R. Jankovic, Vladimir B. Bajic, Le Song, Xin Gao. Poly(A) motif prediction using spectral latent features from human DNA sequences
326 -- 334Yu Peng, Henry C. M. Leung, Siu-Ming Yiu, Ming-Ju Lv, Xin-Guang Zhu, Francis Y. L. Chin. IDBA-tran: a more robust de novo de Bruijn graph assembler for transcriptomes with uneven expression levels
335 -- 343Kousik Kundu, Fabrizio Costa, Rolf Backofen. A graph kernel approach for alignment-free domain-peptide interaction prediction with an application to human SH3 domains
344 -- 351David Golan, Paul Medvedev. Using state machines to model the Ion Torrent sequencing process and to improve read error rates
352 -- 360Derek Aguiar, Sorin Istrail. Haplotype assembly in polyploid genomes and identical by descent shared tracts
361 -- 370Lin Huang, Victoria Popic, Serafim Batzoglou. Short read alignment with populations of genomes
1589 -- 1592Mireia Olivella, Angel Gonzalez, Leonardo Pardo, Xavier Deupi. Relation between sequence and structure in membrane proteins
1593 -- 1599Yoonsoo Hahn. Evidence for the dissemination of cryptic non-coding RNAs transcribed from intronic and intergenic segments by retroposition
1600 -- 1606Matthias Barann, Daniela Esser, Ulrich C. Klostermeier, Tuuli Lappalainen, Anne Luzius, Jan W. P. Kuiper, Ole Ammerpohl, Inga Vater, Reiner Siebert, Vyacheslav Amstislavskiy, Ralf Sudbrak, Hans Lehrach, Stefan Schreiber, Philip Rosenstiel. Janus - a comprehensive tool investigating the two faces of transcription
1607 -- 1613Thomas Schnattinger, Uwe Schöning, Hans A. Kestler. Structural RNA alignment by multi-objective optimization
1614 -- 1622Xiang Chen, Jian-Ding Qiu, Shao-Ping Shi, Sheng-Bao Suo, Shu-Yun Huang, Ru-Ping Liang. Incorporating key position and amino acid residue features to identify general and species-specific Ubiquitin conjugation sites
1623 -- 1630Jan Kirrbach, Miriam Krugliak, Christian L. Ried, Philipp Pagel, Isaiah T. Arkin, Dieter Langosch. Self-interaction of transmembrane helices representing pre-clusters from the human single-span membrane proteins
1631 -- 1637Adam Roberts, Lorian Schaeffer, Lior Pachter. Updating RNA-Seq analyses after re-annotation
1638 -- 1646Martin A. Rijlaarsdam, David J. Rijlaarsdam, Ad J. M. Gillis, Lambert C. J. Dorssers, Leendert H. J. Looijenga. miMsg: a target enrichment algorithm for predicted miR-mRNA interactions based on relative ranking of matched expression data
1647 -- 1653Katja Hebestreit, Martin Dugas, Hans-Ulrich Klein. Detection of significantly differentially methylated regions in targeted bisulfite sequencing data
1654 -- 1662Behnam Neyshabur, Ahmadreza Khadem, Somaye Hashemifar, Seyed Shahriar Arab. NETAL: a new graph-based method for global alignment of protein-protein interaction networks
1663 -- 1670María Jesús García-Godoy, Esteban López-Camacho, Ismael Navas Delgado, José Francisco Aldana Montes. Sharing and executing linked data queries in a collaborative environment
1671 -- 1678Midori A. Harris, Antonia Lock, Jürg Bähler, Stephen G. Oliver, Valerie Wood. FYPO: the fission yeast phenotype ontology
1679 -- 1681Christoph Bartenhagen, Martin Dugas. RSVSim: an R/Bioconductor package for the simulation of structural variations
1682 -- 1684Hákon Jónsson, Aurelien Ginolhac, Mikkel Schubert, Philip L. F. Johnson, Ludovic Orlando. mapDamage2.0: fast approximate Bayesian estimates of ancient DNA damage parameters
1685 -- 1686Clare Sloggett, Nuwan Goonasekera, Enis Afgan. BioBlend: automating pipeline analyses within Galaxy and CloudMan
1687 -- 1689Miriam Rubio-Camarillo, Gonzalo Gómez-López, José M. Fernández, Alfonso Valencia, David G. Pisano. RUbioSeq: a suite of parallelized pipelines to automate exome variation and bisulfite-seq analyses
1690 -- 1692Joseph C. Pearson, Stephen T. Crews. cis-regulatory modules
1693 -- 1695Brett Trost, Ryan Arsenault, Philip Griebel, Scott Napper, Anthony J. Kusalik. DAPPLE: a pipeline for the homology-based prediction of phosphorylation sites
1696 -- 1697Paul Brown, Laura Baxter, Richard Hickman, Jim Beynon, Jonathan D. Moore, Sascha Ott. MEME-LaB: motif analysis in clusters
1698 -- 1699Brian Jiménez-García, Carles Pons, Juan Fernández-Recio. pyDockWEB: a web server for rigid-body protein-protein docking using electrostatics and desolvation scoring
1700 -- 1701Saskia D. Hiltemann, Elizabeth A. McClellan, Jos van Nijnatten, Sebastiaan Horsman, Ivo Palli, Ines Teles Alves, Thomas Hartjes, Jan Trapman, Peter van der Spek, Guido Jenster, Andrew Stubbs. iFUSE: integrated fusion gene explorer
1702 -- 1703Daniel Stöckel, Oliver Müller, Tim Kehl, Andreas Gerasch, Christina Backes, Alexander Rurainski, Andreas Keller, Michael Kaufmann, Hans-Peter Lenhof. NetworkTrail - a web service for identifying and visualizing deregulated subnetworks
1704 -- 1705Louis-Philippe Lemieux Perreault, Sylvie Provost, Marc-André Legault, Amina Barhdadi, Marie-Pierre Dube. pyGenClean: efficient tool for genetic data clean up before association testing
1706 -- 1707Chuan-Yih Yu, Anoop M. Mayampurath, Yunli Hu, Shiyue Zhou, Yehia Mechref, Haixu Tang. Automated annotation and quantification of glycans using liquid chromatography-mass spectrometry
1708 -- 1709Antti Häkkinen, Anantha Barathi Muthukrishnan, Andre Mora, José Manuel Fonseca, Andre S. Ribeiro. Escherichia coli
1710 -- 1712Catherine Voegele, Baptiste Bouchereau, Nivonirina Robinot, James McKay, Philippe Damiecki, Lucile Alteyrac. A universal open-source Electronic Laboratory Notebook

Volume 29, Issue 12

1485 -- 1487Sur Herrera Paredes, Michael F. Melgar, Praveen Sethupathy. Promoter-proximal CCCTC-factor binding is associated with an increase in the transcriptional pausing index
1488 -- 1491Patrick B. F. O'Connor, Gene-Wei Li, Jonathan S. Weissman, John F. Atkins, Pavel V. Baranov. rRNA: mRNA pairing alters the length and the symmetry of mRNA-protected fragments in ribosome profiling experiments
1492 -- 1497Inanç Birol, Anthony Raymond, Shaun D. Jackman, Stephen Pleasance, Robin Coope, Greg A. Taylor, Macaire Man Saint Yuen, Christopher I. Keeling, Dana Brand, Benjamin P. Vandervalk, Heather Kirk, Pawan Pandoh, Richard A. Moore, Yongjun Zhao, Andrew J. Mungall, Barry Jaquish, Alvin Yanchuk, Carol Ritland, Brian Boyle, Jean Bousquet, Kermit Ritland, John MacKay, Jörg Bohlmann, Steven J. M. Jones. Picea glauca) genome from whole-genome shotgun sequencing data
1498 -- 1503Nancy F. Hansen, Jared J. Gartner, Lan Mei, Yardena Samuels, James C. Mullikin. Shimmer: detection of genetic alterations in tumors using next-generation sequence data
1504 -- 1510Hashem A. Shihab, Julian Gough, David N. Cooper, Ian N. M. Day, Tom R. Gaunt. Predicting the functional consequences of cancer-associated amino acid substitutions
1511 -- 1518Lining Ju, Yijie Dylan Wang, Ying Hung, Chien-Fu Jeff Wu, Cheng Zhu. An HMM-based algorithm for evaluating rates of receptor-ligand binding kinetics from thermal fluctuation data
1519 -- 1525Dan J. Woodcock, Keith W. Vance, Michal Komorowski, Georgy Koentges, Bärbel Finkenstädt, David A. Rand. A hierarchical model of transcriptional dynamics allows robust estimation of transcription rates in populations of single cells with variable gene copy number
1526 -- 1533Jennifer Listgarten, Christoph Lippert, Eun Yong Kang, Jing Xiang, Carl Myers Kadie, David Heckerman. A powerful and efficient set test for genetic markers that handles confounders
1534 -- 1540Henrik Failmezger, Paurush Praveen, Achim Tresch, Holger Fröhlich. Learning gene network structure from time laps cell imaging in RNAi Knock downs
1541 -- 1552Ming Wu, Li Liu, Hussein Hijazi, Christina Chan. A multi-layer inference approach to reconstruct condition-specific genes and their regulation
1553 -- 1561Sriganesh Srihari, Mark A. Ragan. Systematic tracking of dysregulated modules identifies novel genes in cancer
1562 -- 1564Christopher Schroeder, Marc Sturm, Andreas Dufke, Ulrike Mau-Holzmann, Thomas Eggermann, Sven Poths, Olaf Riess, Michael Bonin. UPDtool: a tool for detection of iso- and heterodisomy in parent-child trios using SNP microarrays
1565 -- 1567Jia Meng, Xiaodong Cui, Manjeet K. Rao, Yidong Chen, Yufei Huang. Exome-based analysis for RNA epigenome sequencing data
1568 -- 1570Kenneth Lange, Jeanette C. Papp, Janet S. Sinsheimer, Ram Sripracha, Hua Zhou, Eric M. Sobel. Mendel: the Swiss army knife of genetic analysis programs
1571 -- 1573Paola Vera-Licona, Eric Bonnet, Emmanuel Barillot, Andrei Zinovyev. OCSANA: optimal combinations of interventions from network analysis
1574 -- 1576Simone Zorzan, Erika Lorenzetto, Michele Ettorre, Valeria Pontelli, Carlo Laudanna, Mario Buffelli. HOMECAT: consensus homologs mapping for interspecific knowledge transfer and functional genomic data integration
1577 -- 1579Michael J. Meyer, Jishnu Das, Xiujuan Wang, Haiyuan Yu. INstruct: a database of high-quality 3D structurally resolved protein interactome networks
1580 -- 1582Christoph Sommer, Michael Held, Bernd Fischer 0003, Wolfgang Huber, Daniel Gerlich. CellH5: a format for data exchange in high-content screening
1583 -- 1585Robert Smith, Dan Ventura, John T. Prince. Novel algorithms and the benefits of comparative validation
1586 -- 1587Christiana N. Fogg, Diane E. Kovats. International Society for Computational Biology Honors Goncalo Abecasis with Top Bioinformatics/Computational Biology Award for 2013

Volume 29, Issue 11

1361 -- 1366Brendan D. O'Fallon, Whitney Wooderchak-Donahue, David K. Crockett. A support vector machine for identification of single-nucleotide polymorphisms from next-generation sequencing data
1367 -- 1374Sebastian Höhna. Fast simulation of reconstructed phylogenies under global time-dependent birth-death processes
1375 -- 1381Michail Yu. Lobanov, Masha Yu. Suvorina, Nikita V. Dovidchenko, Igor V. Sokolovskiy, Alexey K. Surin, Oxana V. Galzitskaya. A novel web server predicts amino acid residue protection against hydrogen-deuterium exchange
1382 -- 1389Nicoló Fusi, Christoph Lippert, Karsten M. Borgwardt, Neil D. Lawrence, Oliver Stegle. Detecting regulatory gene-environment interactions with unmeasured environmental factors
1390 -- 1398Bo Jiang, Jun S. Liu, Martha L. Bulyk. k-mers
1399 -- 1406Chia-Yen Chen, Samuela Pollack, David J. Hunter, Joel Hirschhorn, Peter Kraft, Alkes L. Price. Improved ancestry inference using weights from external reference panels
1407 -- 1415Bogdan Pasaniuc, Sriram Sankararaman, Dara G. Torgerson, Christopher Gignoux, Noah Zaitlen, Celeste Eng, William Rodriguez-Cintron, Rocio Chapela, Jean G. Ford, Pedro C. Avila, Jose Rodriguez-Santana, Gary K. Chen, Loic Le Marchand, Brian E. Henderson, David Reich, Christopher A. Haiman, Esteban Gonzàlez Burchard, Eran Halperin. Analysis of Latino populations from GALA and MEC studies reveals genomic loci with biased local ancestry estimation
1416 -- 1423Néhémy Lim, Yasin Senbabaoglu, George Michailidis, Florence d'Alché-Buc. OKVAR-Boost: a novel boosting algorithm to infer nonlinear dynamics and interactions in gene regulatory networks
1424 -- 1432Zhixia Teng, Maozu Guo, Xiaoyan Liu, Qiguo Dai, Chun-yu Wang, Ping Xuan. Measuring gene functional similarity based on group-wise comparison of GO terms
1433 -- 1439Chih-Hsuan Wei, Bethany R. Harris, Hung-Yu Kao, Zhiyong Lu. tmVar: a text mining approach for extracting sequence variants in biomedical literature
1440 -- 1447Yufan Guo, Ilona Silins, Ulla Stenius, Anna Korhonen. Active learning-based information structure analysis of full scientific articles and two applications for biomedical literature review
1448 -- 1454Hang Xiao, Hanchuan Peng. APP2: automatic tracing of 3D neuron morphology based on hierarchical pruning of a gray-weighted image distance-tree
1455 -- 1457David H. Silver, Shay Ben-Elazar, Alexei Bogoslavsky, Itai Yanai. de novo genome assembly
1458 -- 1460Yupeng Wang, Jingping Li, Andrew H. Paterson. MCScanX-transposed: detecting transposed gene duplications based on multiple colinearity scans
1461 -- 1462Yuhao Shi, Jacek Majewski. FishingCNV: a graphical software package for detecting rare copy number variations in exome-sequencing data
1463 -- 1464Jinyan Huang, Jun Chen, Mark Lathrop, Liming Liang. A tool for RNA sequencing sample identity check
1465 -- 1466Jake Y. Fried, Martijn P. van Iersel, Mirit I. Aladjem, Kurt W. Kohn, Augustin Luna. PathVisio-Faceted Search: an exploration tool for multi-dimensional navigation of large pathways
1467 -- 1468Falko Krause, Marvin Schulz, Ben Ripkens, Max Flöttmann, Marcus Krantz, Edda Klipp, Thomas Handorf. Biographer: web-based editing and rendering of SBGN compliant biochemical networks
1469 -- 1470Jens Einloft, Jörg Ackermann, Joachim Nöthen, Ina Koch. MonaLisa - visualization and analysis of functional modules in biochemical networks
1471 -- 1473Tim Kacprowski, Nadezhda T. Doncheva, Mario Albrecht. NetworkPrioritizer: a versatile tool for network-based prioritization of candidate disease genes or other molecules
1474 -- 1476Hiromu Takizawa, Kazushige Nakamura, Akito Tabira, Yoichi Chikahara, Tatsuhiro Matsui, Noriko Hiroi, Akira Funahashi. LibSBMLSim: a reference implementation of fully functional SBML simulator
1477 -- 1480Pieter Libin, Gertjan Beheydt, Koen Deforche, Stijn Imbrechts, Fossie Ferreira, Kristel Van Laethem, Kristof Theys, Ana Patricia Carvalho, Joana Cavaco-Silva, Giuseppe Lapadula, Carlo Torti, Matthias Assel, Stefan Wesner, Joke Snoeck, Jean Ruelle, Annelies De Bel, Patrick Lacor, Paul De Munter, Eric Van Wijngaerden, Maurizio Zazzi, Rolf Kaiser, Ahidjo Ayouba, Martine Peeters, Tulio de Oliveira, Luiz Carlos Junior Alcantara, Zehava Grossman, Peter M. A. Sloot, Dan Otelea, Simona Paraschiv, Charles A. Boucher, Ricardo Camacho, Anne-Mieke Vandamme. RegaDB: community-driven data management and analysis for infectious diseases
1481 -- 1483Sanghoon Moon, Kwang Su Jung, Young-Jin Kim, Mi Yeong Hwang, Kyungsook Han, Jong-Young Lee, Kiejung Park, Bong-Jo Kim. KGVDB: a population-based genomic map of CNVs tagged by SNPs in Koreans
1484 -- 0Manal Kalkatawi, Farania Rangkuti, Michael Schramm, Boris R. Jankovic, Allan Kamau, Rajesh Chowdhary, John A. C. Archer, Vladimir B. Bajic. Dragon PolyA Spotter: predictor of poly(A) motifs within human genomic DNA sequences

Volume 29, Issue 10

1241 -- 1249Chen Lu, Jeanne Latourelle, George T. O'Connor, Josée Dupuis, Eric D. Kolaczyk. Network-guided sparse regression modeling for detection of gene-by-gene interactions
1250 -- 1259Ergude Bao, Tao Jiang, Thomas Girke. BRANCH: boosting RNA-Seq assemblies with partial or related genomic sequences
1260 -- 1267Martin S. Lindner, Maximilian Kollock, Franziska Zickmann, Bernhard Y. Renard. Analyzing genome coverage profiles with applications to quality control in metagenomics
1268 -- 1274Marco Pagni, Hélène Niculita-Hirzel, Loïc Pellissier, Anne Dubuis, Ioannis Xenarios, Antoine Guisan, Ian R. Sanders, Jérôme Goudet, Nicolas Guex. Density-based hierarchical clustering of pyro-sequences on a large scale - the case of fungal ITS1
1275 -- 1282Danni Yu, Wolfgang Huber, Olga Vitek. Shrinkage estimation of dispersion in Negative Binomial models for RNA-seq experiments with small sample size
1283 -- 1291Tarmo Äijö, Kirsi Granberg, Harri Lähdesmäki. Sorad: a systems biology approach to predict and modulate dynamic signaling pathway response from phosphoproteome time-course measurements
1292 -- 1298Bjørn Olav Hald, Morten Garkier Hendriksen, Preben Graae Sørensen. Programming strategy for efficient modeling of dynamics in a population of heterogeneous cells
1299 -- 1307Ivan Chang, Pierre Baldi. A unifying kinetic framework for modeling oxidoreductase-catalyzed reactions
1308 -- 1316Lieven P. C. Verbeke, Lore Cloots, Piet Demeester, Jan Fostier, Kathleen Marchal. EPSILON: an eQTL prioritization framework using similarity measures derived from local networks
1317 -- 1324Yong-Cui Wang, Shi-Long Chen, Nai-Yang Deng, Yong Wang. Network predicting drug's anatomical therapeutic chemical code
1325 -- 1332Jon C. Ison, Matús Kalas, Inge Jonassen, Dan M. Bolser, Mahmut Uludag, Hamish McWilliam, James Malone, Rodrigo Lopez, Steve Pettifer, Peter M. Rice. EDAM: an ontology of bioinformatics operations, types of data and identifiers, topics and formats
1333 -- 1340David E. Robbins, Alexander Grüneberg, Helena F. Deus, Murat M. Tanik, Jonas S. Almeida. A self-updating road map of The Cancer Genome Atlas
1341 -- 1342Glenn Hickey, Benedict Paten, Dent Earl, Daniel Zerbino, David Haussler. HAL: a hierarchical format for storing and analyzing multiple genome alignments
1343 -- 1344Diogo Borges, Yasset Pérez-Riverol, Fabio C. S. Nogueira, Gilberto B. Domont, Jesus Noda, Felipe da Veiga Leprevost, Vladimir Besada, Felipe M. G. França, Valmir C. Barbosa, Aniel Sánchez, Paulo C. Carvalho. Effectively addressing complex proteomic search spaces with peptide spectrum matching
1345 -- 1347Gerald Weber. TfReg: calculating DNA and RNA melting temperatures and opening profiles with mesoscopic models
1348 -- 1349Vincent Navratil, Clément Pontoizeau, Elise Billoir, Benjamin J. Blaise. SRV: an open-source toolbox to accelerate the recovery of metabolic biomarkers and correlations from metabolic phenotyping datasets
1350 -- 1351Samad Lotia, Jason Montojo, Yue Dong, Gary D. Bader, Alexander R. Pico. Cytoscape App Store
1352 -- 1354Hanfei Sun, Bo Qin, Tao Liu, Qixuan Wang, Jing Liu, Juan Wang, Xueqiu Lin, Yulin Yang, Len Taing, Prakash K. Rao, Myles Brown, Yong Zhang, Henry Long, X. Shirley Liu. CistromeFinder for ChIP-seq and DNase-seq data reuse
1355 -- 1356Amit Zeisel, Assif Yitzhaky, Noa Bossel Ben-Moshe, Eytan Domany. An accessible database for mouse and human whole transcriptome qPCR primers
1357 -- 1358Saliha Durmus Tekir, Tunahan Çakir, Emre Ardiç, Ali Semih Sayilirbas, Gökhan Konuk, Mithat Konuk, Hasret Sariyer, Azat Ugurlu, Ilknur Karadeniz, Arzucan Özgür, Fatih Erdogan Sevilgen, Kutlu Ö. Ülgen. PHISTO: pathogen-host interaction search tool
1359 -- 1360Richard J. Giuly, Keun-Young Kim, Mark H. Ellisman. DP2: Distributed 3D image segmentation using micro-labor workforce

Volume 29, Issue 1

1 -- 7Ryan M. Layer, Kevin Skadron, Gabriel Robins, Ira M. Hall, Aaron R. Quinlan. Binary Interval Search: a scalable algorithm for counting interval intersections
8 -- 14Massimo Andreatta, Ole Lund, Morten Nielsen. Simultaneous alignment and clustering of peptide data using a Gibbs sampling approach
15 -- 21Alexander Dobin, Carrie A. Davis, Felix Schlesinger, Jorg Drenkow, Chris Zaleski, Sonali Jha, Philippe Batut, Mark Chaisson, Thomas R. Gingeras. STAR: ultrafast universal RNA-seq aligner
22 -- 28Russell Bonneville, Victor X. Jin. A hidden Markov model to identify combinatorial epigenetic regulation patterns for estrogen receptor α target genes
29 -- 38Wenhui Wang, Xiaolin Yin, Yoon Soo Pyon, Matthew Hayes, Jing Li. Rare variant discovery and calling by sequencing pooled samples with overlaps
39 -- 46Ahmed M. Mehdi, Muhammad Shoaib B. Sehgal, Bostjan Kobe, Timothy L. Bailey, Mikael Bodén. DLocalMotif: a discriminative approach for discovering local motifs in protein sequences
47 -- 53Alex W. Slater, Javier I. Castellanos, Manfred J. Sippl, Francisco Melo. Towards the development of standardized methods for comparison, ranking and evaluation of structure alignments
54 -- 61Jamie R. Hill, Charlotte M. Deane. MP-T: improving membrane protein alignment for structure prediction
62 -- 68Benjamin Merget, David Zilian, Tobias Müller, Christoph A. Sotriffer. Mycobacterium tuberculosis permeability prediction tool for small molecules
69 -- 76Thomas L. Vincent, Peter J. Green, Derek N. Woolfson. LOGICOIL - multi-state prediction of coiled-coil oligomeric state
77 -- 83Florian Erhard, Lars Dölken, Ralf Zimmer. RIP-chip enrichment analysis
84 -- 91Androniki Menelaou, Jonathan Marchini. Genotype calling and phasing using next-generation sequencing reads and a haplotype scaffold
92 -- 98Chia-Hsin Liu, Ker-Chau Li, Shinsheng Yuan. Human protein-protein interaction prediction by a novel sequence-based co-evolution method: co-evolutionary divergence
99 -- 105Xi Chen, Hemant Ishwaran. Pathway hunting by random survival forests
106 -- 113Xiujun Zhang, Keqin Liu, Zhi-Ping Liu, Béatrice Duval, Jean-Michel Richer, Xing-Ming Zhao, Jin-Kao Hao, Luonan Chen. NARROMI: a noise and redundancy reduction technique improves accuracy of gene regulatory network inference
114 -- 116Shiyuyun Tang, Ivan Antonov, Mark Borodovsky. MetaGeneTack: ab initio detection of frameshifts in metagenomic sequences
117 -- 118Arturo Magana-Mora, Haitham Ashoor, Boris R. Jankovic, Allan Kamau, Karim Awara, Rajesh Chowdhary, John A. C. Archer, Vladimir B. Bajic. Dragon TIS Spotter: an Arabidopsis-derived predictor of translation initiation sites in plants
119 -- 121Yukiteru Ono, Kiyoshi Asai, Michiaki Hamada. PBSIM: PacBio reads simulator - toward accurate genome assembly
122 -- 123Zhengwei Zhu, Beifang Niu, Jing Chen, Sitao Wu, Shulei Sun, Weizhong Li. MGAviewer: a desktop visualization tool for analysis of metagenomics alignment data
124 -- 125Lu Zhang, Jing Zhang, Jing Yang, Dingge Ying, Yu-Lung Lau, Wanling Yang. PriVar: a toolkit for prioritizing SNVs and indels from next-generation sequencing data
126 -- 128Dimitrios Vlachakis, Dimosthenis Tsagkrasoulis, Vasileios Megalooikonomou, Sophia Kossida. Introducing Drugster: a comprehensive and fully integrated drug design, lead and structure optimization toolkit
129 -- 131Mario Fasold, Hans Binder. AffyRNADegradation: control and correction of RNA quality effects in GeneChip expression data
132 -- 134Clare Pacini, Francesco Iorio, Emanuel J. V. Gonçalves, Murat Iskar, Thomas Klabunde, Peer Bork, Julio Saez-Rodriguez. DvD: An R/Cytoscape pipeline for drug repurposing using public repositories of gene expression data
135 -- 136Hailiang Huang, Sandeep Tata, Robert J. Prill. BlueSNP: R package for highly scalable genome-wide association studies using Hadoop clusters
137 -- 139Masao Nagasaki, André Fujita, Yayoi Sekiya, Ayumu Saito, Emi Ikeda, Chen Li 0007, Satoru Miyano. XiP: a computational environment to create, extend and share workflows
140 -- 142Patrick W. Sheppard, Muruhan Rathinam, Mustafa Khammash. SPSens: a software package for stochastic parameter sensitivity analysis of biochemical reaction networks
143 -- 145Michael Weitzel, Katharina Nöh, Tolga Dalman, Sebastian Niedenführ, Birgit Stute, Wolfgang Wiechert. 13C-metabolic flux analysis
146 -- 147Mark Woodbridge, Christopher D. Tomlinson, Sarah A. Butcher. ADAM: automated data management for research datasets