cnv

Here are 3 public repositories matching this topic...

nf-cmgg / structural

A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads

annotation repeats ngs cnv cram structural-variation ngs-pipeline nextflow-pipeline short-reads

Updated Sep 9, 2026
Nextflow

assane-mbodj / dupfinder

Star

DupFinder: A tools to detect the duplicated genes using Illumina and Nanopore sequencing data

bioinformatics genomics ngs sequencing cnv structural-variation-calling duplicated-gene

Updated Mar 3, 2025
Nextflow

TRON-Bioinformatics / tronflow-copy-number-calling

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A nextflow workflow for copy number calling

bioinformatics cnv

Updated Jan 14, 2026
Nextflow

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