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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)vcfhelpR
Functions to order, write and crossmap VCF/BED records in RgtexRNA
Gene expression retrieval with GTEx APIepacts-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