Characterization of Germline variants
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Updated
Mar 15, 2022 - Python
Characterization of Germline variants
Snakemake-based workflow for detecting structural variants in genomic data
Clinical Whole Genome and Exome Sequencing Pipeline
Snakemake workflow to call germline variant
Screening deleterious germline variants (DGVs) in WCM UC cohort
Tool for automated classification of genetic variants according to ACMG criteria.
Super fast conversion of GVF file format to VCF file format
Depository for Bioinformatics Master Project HT2022-VT2023
Snakemake based workflow for analysis of dnaseq data for calling germline/somatic mutations
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