There are no reviews yet. Be the first to send feedback to the community and the maintainers!
pcgr
Personal Cancer Genome Reporter (PCGR)cpsr
Cancer Predisposition Sequencing Reporter (CPSR)gvanno
Generic human DNA variant annotation pipelineoncoEnrichR
Explore the cancer relevance of your gene listvcf2tsvpy
Genomic VCF to tab-separated valuespharmOncoX
Targeted and non-targeted anticancer drugs and drug regimenscacao
Callable Cancer Loci - assessment of sequencing coverage for actionable and pathogenic loci in cancerphenOncoX
Crossmapped phenotype ontologies for the oncology domaingeneOncoX
Human gene annotations for the oncology domaincancerHotspots
R data package with mutational hotspots in cancersv_anno
Processing and annotation of somatic structural variantsplsd
Prospective Lynch Syndrome Database (PLSD) - cumulative risk for cancer by age, genetic variant, and gendergwasOncoX
Cancer variant data from genome-wide association studies (GWAS)sigven.github.io
Minimal personal websitelscarisk
Estimation of cancer risk in Lynch Syndrome carriers (PLSD Shiny web application)vcfmerge
MuTect2 + Strelka somatic VCF mergervcfhelpR
Functions to order, write and crossmap VCF/BED records in Repacts-docker
Dockerized version of EPACTSliteratureVault
Biomedical literature reference data for precision cancer medicineLove Open Source and this site? Check out how you can help us