Identification of deleterious synonymous variants in human genomes
Gene-set analysis is severely biased when applied to genome-wide methylation data
SPANNER: taxonomic assignment of sequences using pyramid matching of similarity profiles
DeMix: deconvolution for mixed cancer transcriptomes using raw measured data
Network2Canvas: network visualization on a canvas with enrichment analysis
Improved image alignment method in application to X-ray images and biological images
PurBayes: estimating tumor cellularity and subclonality in next-generation sequencing data
SVGenes: a library for rendering genomic features in scalable vector graphic format
NGS++: a library for rapid prototyping of epigenomics software tools
Triplex-Inspector: an analysis tool for triplex-mediated targeting of genomic loci
miRTCat: a comprehensive map of human and mouse microRNA target sites including non-canonical nucleation bulges
Triplex: an R/Bioconductor package for identification and visualization of potential intramolecular triplex patterns in DNA sequences
viRome: an R package for the visualization and analysis of viral small RNA sequence datasets
EpiCombFlu: exploring known influenza epitopes and their combination to design a universal influenza vaccine
Mutascope: sensitive detection of somatic mutations from deep amplicon sequencing
HitPick: a web server for hit identification and target prediction of chemical screenings
PIUS: peptide identification by unbiased search
BeCAS: biomedical concept recognition services and visualization
EcoGene-RefSeq: EcoGene tools applied to the RefSeq prokaryotic genomes
iAnn: an event sharing platform for the life sciences
Relating genes to function: identifying enriched transcription factors using the ENCODE ChIP-Seq significance tool