Journal: Bioinformatics

Volume 31, Issue 15

2421 -- 2425Raquel M. Silva, Diogo Pratas, Luísa Castro, Armando J. Pinho, Paulo Jorge S. G. Ferreira. Three minimal sequences found in Ebola virus genomes and absent from human DNA
2426 -- 2433Michiaki Hamada, Yukiteru Ono, Ryohei Fujimaki, Kiyoshi Asai. Learning chromatin states with factorized information criteria
2434 -- 2442Zheng Xu, Qing Duan, Song Yan, Wei Chen, Mingyao Li, Ethan M. Lange, Yun Li. DISSCO: direct imputation of summary statistics allowing covariates
2443 -- 2451Emanuele Bosi, Beatrice Donati, Marco Galardini, Sara Brunetti, Marie-France Sagot, Pietro Liò, Pierluigi Crescenzi, Renato Fani, Marco Fondi. MeDuSa: a multi-draft based scaffolder
2452 -- 2460Bayarbaatar Amgalan, Hyunju Lee. DEOD: uncovering dominant effects of cancer-driver genes based on a partial covariance selection method
2461 -- 2468Brendan J. Kelly, Robert Gross, Kyle Bittinger, Scott Sherrill-Mix, James D. Lewis, Ronald G. Collman, Frederic D. Bushman, Hongzhe Li. Power and sample-size estimation for microbiome studies using pairwise distances and PERMANOVA
2469 -- 2474Amit K. Chattopadhyay, Diar Nasiev, Darren R. Flower. A statistical physics perspective on alignment-independent protein sequence comparison
2475 -- 2481Quan Zou, Qinghua Hu, Maozu Guo, Guohua Wang. HAlign: Fast multiple similar DNA/RNA sequence alignment based on the centre star strategy
2482 -- 2488Dries Decap, Joke Reumers, Charlotte Herzeel, Pascal Costanza, Jan Fostier. Halvade: scalable sequence analysis with MapReduce
2489 -- 2496Sebastian Will, Christina Otto, Milad Miladi, Mathias Möhl, Rolf Backofen. SPARSE: quadratic time simultaneous alignment and folding of RNAs without sequence-based heuristics
2497 -- 2504Matti Pirinen, Tuuli Lappalainen, Noah A. Zaitlen, Emmanouil T. Dermitzakis, Peter Donnelly, Mark I. McCarthy, Manuel A. Rivas. Assessing allele-specific expression across multiple tissues from RNA-seq read data
2505 -- 2513Swapna Agarwal, Pradip Ghanty, Nikhil R. Pal. Identification of a small set of plasma signalling proteins using neural network for prediction of Alzheimer's disease
2514 -- 2522Francesca Gullo, Mark van der Garde, Giulia Russo, Marzio Pennisi, Santo Motta, Francesco Pappalardo, Suzanne Watt. + hematopoietic stem/progenitor cells with different cytokine combinations
2523 -- 2529Songpeng Zu, Ting Chen, Shao Li. Global optimization-based inference of chemogenomic features from drug-target interactions
2530 -- 2536Yawwani Gunawardana, Shuhei Fujiwara, Akiko Takeda, Jeongmin Woo, Christopher Woelk, Mahesan Niranjan. Outlier detection at the transcriptome-proteome interface
2537 -- 2544Fan Zhu, Lihong Shi, James Douglas Engel, Yuanfang Guan. Regulatory network inferred using expression data of small sample size: application and validation in erythroid system
2545 -- 2552Joan Segura, Carlos Oscar Sánchez Sorzano, Jesús Cuenca Alba, Patrick Aloy, José María Carazo. Using neighborhood cohesiveness to infer interactions between protein domains
2553 -- 2559Longendri Aguilera-Mendoza, Yovani Marrero-Ponce, Roberto Tellez-Ibarra, Monica T. Llorente-Quesada, Jesús Salgado, Stephen J. Barigye, Jun Liu. Overlap and diversity in antimicrobial peptide databases: compiling a non-redundant set of sequences
2560 -- 2564Li Teng, Bing He, Jiahui Wang, Kai Tan. 4DGenome: a comprehensive database of chromatin interactions
2565 -- 2567Graham J. Etherington, Ricardo H. Ramirez-Gonzalez, Dan MacLean. bio-samtools 2: a package for analysis and visualization of sequence and alignment data with SAMtools in Ruby
2568 -- 2570Shahar Alon, Muhammad Erew, Eli Eisenberg. DREAM: a webserver for the identification of editing sites in mature miRNAs using deep sequencing data
2571 -- 2573Bachir Balech, Saverio Vicario, Giacinto Donvito, Alfonso Monaco, Pasquale Notarangelo, Graziano Pesole. MSA-PAD: DNA multiple sequence alignment framework based on PFAM accessed domain information
2574 -- 2576Johannes Palme, Sepp Hochreiter, Ulrich Bodenhofer. KeBABS: an R package for kernel-based analysis of biological sequences
2577 -- 2579Alexey M. Kozlov, Andre J. Aberer, Alexandros Stamatakis. ExaML version 3: a tool for phylogenomic analyses on supercomputers
2580 -- 2582Greet De Baets, Joost J. J. van Durme, Rob van der Kant, Joost Schymkowitz, Frederic Rousseau. Solubis: optimize your protein
2583 -- 2585Rajendra Kumar, Helmut Grubmüller. do_x3dna: a tool to analyze structural fluctuations of dsDNA or dsRNA from molecular dynamics simulations
2586 -- 2588Rachel Legendre, Agnès Baudin-Baillieu, Isabelle Hatin, Olivier Namy. RiboTools: a Galaxy toolbox for qualitative ribosome profiling analysis
2589 -- 2590Emmanuel Dimont, Jiantao Shi, Rory Kirchner, Winston Hide. edgeRun: an R package for sensitive, functionally relevant differential expression discovery using an unconditional exact test
2591 -- 2594Quan Wang, Hui Yu, Zhongming Zhao, Peilin Jia. EW_dmGWAS: edge-weighted dense module search for genome-wide association studies and gene expression profiles
2595 -- 2597Jan Grau, Ivo Grosse, Jens Keilwagen. PRROC: computing and visualizing precision-recall and receiver operating characteristic curves in R
2598 -- 2600Wenkang Huang, Guanqiao Wang, Qiancheng Shen, Xinyi Liu, Shaoyong Lu, Lv Geng, Zhimin Huang, Jian Zhang. ASBench: benchmarking sets for allosteric discovery