Individual skill
snpeff-variant-annotation
Annotate and filter VCF variants with SnpEff and SnpSift. SnpEff predicts functional effects (HIGH/MODERATE/LOW/MODIFIER), genes, transcripts, AA changes, HGVS; SnpSift filters and adds ClinVar/dbSNP. Java CLI with Python subprocess integration. Use ANNOVAR for multi-database annotation; Ensembl VEP for REST API; SnpEff for fast CLI with pre-built genomes.
skills/genomics-bioinformatics/variant/snpeff-variant-annotation/SKILL.md
Source commit 55c1bd3e863d11bf5a853d24bcdda10c88e6eddf
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- Observed behavior
- Not checked yet
- Last checked
- Nov 5, 2026
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Repository context
- Repository stars (not skill ratings)
- 386
- Repository last updated
- Nov 4, 2026
- License
- NOASSERTION
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- ai-agent Repository topic
- bioinformatics Repository topic
- claude-code Repository topic
- claude-plugin Repository topic
- drug-discovery Repository topic
- genomics Repository topic
- life-sciences Repository topic
- scientific-computing Repository topic
- claude-skills Repository topic
- open-source Repository topic
- data Derived category
- data-databases Derived category
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