cnv

Here are 4 public repositories matching this topic...

(current) Comprehensive WGS omics analysis pipeline ( reads to variants & QC ) : Sequence Platforms ( Illumina, PacBio, ONT, Ultima, Roche )

snakemake ngs pacbio wgs snv illumina cnv sv qc ont aws-spot fsx-lustre

MSDS Thesis - Pan-Collagen Survival Analysis of CNV in Ovarian Cancer

Workflow and scripts related to WGS analysis

shiny-apps wgs cnv

Reproducible, containerized GRCh38 pipeline for annotation and comparison of synthetic SNVs and CNVs across four rare diseases.

bioinformatics genomics reproducible-research vcf cnv variant-annotation grch38 rare-disease apptainer

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