Journal: Bioinformatics

Volume 32, Issue 14

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