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bio-copy-number-cnvkit-analysis

maintained by GPTomics

star 299 account_tree 51 verified_user MIT License
bolt View GitHub
Overview Implementation Examples History

Detect copy number variants from targeted/exome sequencing using CNVkit. Supports tumor-normal pairs, tumor-only, and germline CNV calling. Use for WES or targeted panel sequencing.

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Skill Details

GitHub Stars 299
GitHub Forks 51
Created Jan 2026
Last Updated il y a 5 mois
tools tools bioinformatics

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