A python parser to simplify and build the VCF (Variant Call Format).
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Updated
Dec 15, 2020 - Python
A python parser to simplify and build the VCF (Variant Call Format).
Clinical Whole Genome and Exome Sequencing Pipeline
Human mitochondrial variants annotation using HmtVar.
Library for indexing VCF files for random access searches by rsID
The DKFZ-ODCF, formerly DKFZ/eilslabs SNV-Calling Workflow
Neighborhood-Aware Variant Impact Predictor
GPF: Genotypes and Phenotypes in Families
OpenCRAVAT as a GenePattern module
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