bio-long-read-sequencing-clair3-variants

FridrichMethod/awesome-skills

SkillLoads cleanly

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,…

Scores
out of 100 · grade B+

2026-08-18

Works

40% of the score

100/100

Loads cleanly: valid frontmatter, required fields present, no dangling references.

Maintained

25% of the score

94/100

no commits in the last 12 weeks
no license file

Adopted

20% of the score

16/100

13 stars on the source repo.

Documented

15% of the score

84/100

769 words with worked examples.
Ships 2 bundled files.

Loads cleanly. Every structural check Claude Code needs to register this passed. Last commit 2 days ago.

Install

npx skills add FridrichMethod/awesome-skills/bio-long-read-sequencing-clair3-variants

What the check found

Every finding on this listing, and what each one means for whether it loads.
Finding	What it means
No license	The repository ships no license file, so the reuse terms are unclear.

What it says it does

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.

Every number above came out of reading the file and its repository. Nothing is a judgement call, nothing is a model’s opinion, and nothing can be paid for. The full method is published. Source last committed 2026-08-16.

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