🎉 CNVetti – robust, efficient, and versatile clinical CNV calling from HTS data

This software package allows the calling of copy number variations (CNV) from high-throughput sequencing (HTS) data. It provides this functionality for various types of data and experimental designs in both germline and somatic calling.

Quick Facts

Supported OS: Linux
License: GPL v3
Status: Alpha

Upcoming Features

Installation via Bioconda

Name		Name	Last commit message	Last commit date
Latest commit History 33 Commits
cnvetti		cnvetti
lib-coverage		lib-coverage
lib-debias		lib-debias
lib-discover		lib-discover
lib-filter		lib-filter
lib-genotype		lib-genotype
lib-merge-cov		lib-merge-cov
lib-merge-seg		lib-merge-seg
lib-mod-cov		lib-mod-cov
lib-model-pool		lib-model-pool
lib-model-wis		lib-model-wis
lib-normalize		lib-normalize
lib-shared		lib-shared
lib-visualize		lib-visualize
.gitignore		.gitignore
.travis.yml		.travis.yml
CHANGELOG.md		CHANGELOG.md
Cargo.toml		Cargo.toml
LICENSE.txt		LICENSE.txt
README.md		README.md

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🎉 CNVetti – robust, efficient, and versatile clinical CNV calling from HTS data

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