7 projects
VAFator
Annotate variants in a VCF file with technical annotations from one or more BAMs
neofox
NEOantigen Feature tOolboX
covigator
clinical-variant-ark
A Python client for the Clinical Variant Ark
pyeasyfuse
EasyFuse is a pipeline to detect fusion transcripts from RNA-seq data with high accuracy.
gel-coverage
Whole genome coverage analysis tool
vcf-dedup
Removal of duplicated variants from a VCF
