This is your work, valued
research scientist - precision cancer medicine // genomics // cancer data science
pcgr. Personal Cancer Genome Reporter (PCGR)
281cpsr. Cancer Predisposition Sequencing Reporter (CPSR)
64gvanno. Generic human DNA variant annotation pipeline
60oncoEnrichR. Explore the cancer relevance of your gene list
54vcf2tsvpy. Genomic VCF to tab-separated values
49pharmOncoX. Targeted and non-targeted anticancer drugs and drug regimens
31cacao. Callable Cancer Loci - assessment of sequencing coverage for actionable and pathogenic loci in cancer
21phenOncoX. Crossmapped phenotype ontologies for the oncology domain
16geneOncoX. Human gene annotations for the oncology domain
6gwasOncoX. Cancer variant data from genome-wide association studies (GWAS)
3cancerHotspots. R data package with mutational hotspots in cancer
3plsd. Prospective Lynch Syndrome Database (PLSD) - cumulative risk for cancer by age, genetic variant, and gender
3vcfmerge. MuTect2 + Strelka somatic VCF merger
2sv_anno. Processing and annotation of somatic structural variants
2literatureVault. Biomedical literature reference data for precision cancer medicine
1portfolio. 🚀 Create a dynamic portfolio by just providing your GitHub username.
1gganatogram. Create anatograms using ggplot2
1vcfhelpR. Functions to order, write and crossmap VCF/BED records in R
1epacts-docker. Dockerized version of EPACTS
1gtexRNA. Gene expression retrieval with GTEx API
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