Software

A list of tools developed by the CNIO Bioinformatics Unit

APPRIS

The APPRIS database and web services annotate alternative splice variants and select a single variant as the main (principal) isoform.

Rodriguez J. M. et al. 2022. PMID: 34755885

BEYONDCELL

A computational methodology for identifying and treating tumour cell subpopulations with distinct drug responses in single-cell RNA-seq data.

Fustero-Torre C. et al. 2021. PMID: 34911571

BICYCLE

A stand-alone and multiplatform application for bisulfite-seq analysis.

Graña O. et al. 2017. PMID: 29211825

BOLLITO

A comprehensive, end-to-end Snakemake pipeline for single cell RNA-seq.

García-Jimeno L. et al. PMID: 34788788

DREIMT

A tool for prioritization of drugs capable of modulating the immune system.

Troulé K. et al. 2020. PMID: 32818254

NEXTPRESSO

A comprehensive RNA-seq data analysis workflow.

Graña O. et al. 2017. Link

PANDRUGS

A platform to guide the selection of therapies from the results of genome-wide studies in cancer disease.

Jiménez-Santos M. J. et al. 2023. PMID: 37207338

TRIFID

A method to assess the functional relevance of splice isoforms.

Pozo F. et al. 2021. PMID: 34046593

VARCA

A pipeline for targeted DNAseq variant detection.

VULCANSPOT

A method for detecting and targeting cancer genetic dependencies.

Perales-Patón J. et al. 2019. PMID: 31173067