The APPRIS database and web services annotate alternative splice variants and select a single variant as the main (principal) isoform.
A computational methodology for identifying and treating tumour cell subpopulations with distinct drug responses in single-cell RNA-seq data.
A stand-alone and multiplatform application for bisulfite-seq analysis
A comprehensive, end-to-end Snakemake pipeline for single cell RNA-seq.
A tool for prioritization of drugs capable of modulating the immune system.
A platform to guide the selection of therapies from the results of genome-wide studies in cancer disease.
A comprehensive RNA-seq data analysis workflow, comprising the most common needs demanded by experimental biologists.
A pipeline for targeted DNAseq variant detection.
A method to assess the functional relevance of splice isoforms
A method for detecting and targeting cancer genetic dependencies.