Bio Long Read Sequencing Clair3 Variants

About this skill

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

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Content SHA-256: e21620f776a4727e2324142f4ff1a26f4b87494d384d9e8346e22ac2ed807017

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Original listing metadata

Original name

bio-long-read-sequencing-clair3-variants

Original description

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 — from majiayu000/claude-skill-registry

About this listing

Category: Science & research
Reported license: MIT
Listing language (estimated): English
Review status: Not individually reviewed
Agent compatibility: Atlas installation supports Claude Code, Codex, and Cursor. Skill-specific dependencies and features are checked during setup.