Snakemake workflow to call germline variant
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Updated
Oct 15, 2019 - Python
Snakemake workflow to call germline variant
Super fast conversion of GVF file format to VCF file format
Depository for Bioinformatics Master Project HT2022-VT2023
Tool for automated classification of genetic variants according to ACMG criteria.
Screening deleterious germline variants (DGVs) in WCM UC cohort
Snakemake based workflow for analysis of dnaseq data for calling germline/somatic mutations
Clinical Whole Genome and Exome Sequencing Pipeline
Snakemake-based workflow for detecting structural variants in genomic data
Characterization of Germline variants
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