- VIST - a Variant-Information Search Tool for precision oncology
- RF_Purify: a novel tool for comprehensive analysis of tumor-purity in methylation array data based on random forest regression
- Multitask learning for biomedical named entity recognition with cross-sharing structure
- baerhunter: An R package for the discovery and analysis of expressed non-coding regions in bacterial RNA-seq data
- LightDock goes information-driven
- StrainHub: A phylogenetic tool to construct pathogen transmission networks
- MEPSAnd: Minimum Energy Path Surface Analysis over n-dimensional surfaces
- AntiHIV-Pred: Web-resource for in silico prediction of anti-HIV/AIDS activity
- Benchmarking software tools for detecting and quantifying selection in evolve and resequencing studies
- An enhanced genetic model of colorectal cancer progression history
- AlleleAnalyzer: a tool for personalized and allele-specific sgRNA design
- Multiple-kernel learning for genomic data mining and prediction
- Indirect association and ranking hypotheses for literature based discovery
- FQStat: a parallel architecture for very high-speed assessment of sequencing quality metrics
- Benchmarking software tools for detecting and quantifying selection in evolve and resequencing studies
- An enhanced genetic model of colorectal cancer progression history
- AlleleAnalyzer: a tool for personalized and allele-specific sgRNA design
- scAlign: a tool for alignment, integration, and rare cell identification from scRNA-seq data
- Screening for genes that accelerate the epigenetic aging clock in humans reveals a role for the H3K36 methyltransferase NSD1
- Additional Neural Matrix Factorization model for computational drug repositioning
Whats new in Bioinformatics
Genome Biology
- Benchmarking software tools for detecting and quantifying selection in evolve and resequencing studies
- An enhanced genetic model of colorectal cancer progression history
- AlleleAnalyzer: a tool for personalized and allele-specific sgRNA design
- scAlign: a tool for alignment, integration, and rare cell identification from scRNA-seq data
- Screening for genes that accelerate the epigenetic aging clock in humans reveals a role for the H3K36 methyltransferase NSD1
- BERMUDA: a novel deep transfer learning method for single-cell RNA sequencing batch correction reveals hidden high-resolution cellular subtypes
- The bio.tools registry of software tools and data resources for the life sciences
- Analysis of Vibrio cholerae genomes identifies new type VI secretion system gene clusters
- Quantitative principles of cis-translational control by general mRNA sequence features in eukaryotes
- Correction to: Ancient polymorphisms contribute to genome-wide variation by long-term balancing selection and divergent sorting in Boechera stricta