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bio-long-read-sequencing-clair3-variants

maintained by GPTomics

star 300 account_tree 51 verified_user MIT License
bolt View GitHub
Overview Implementation Examples History

Deep learning-based variant calling from long reads using Clair3 for SNPs and small indels. Use when calling germline variants from ONT or PacBio alignments, particularly when high accuracy is needed for clinical or research applications.

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Skill Details

GitHub Stars 300
GitHub Forks 51
Created Jan 2026
Last Updated 5个月前
tools tools bioinformatics

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