7 projects
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.
vafator
Annotate a VCF file with AF, AD and DP from tumor and normal BAMs
gel-coverage
Whole genome coverage analysis tool
vcf-dedup
Removal of duplicated variants from a VCF
