Neoantigen Prediction (bioSkills)
A Claude Code skill that builds a tumor-to-candidate neoantigen pipeline with pVACtools, emphasizing that binding prediction is the easy part and true positives live downstream.
| Type | Claude Skill |
| Supplier | GPTomics bioSkills (community OSS, MIT) |
| Availability | GA — part of the bioSkills collection |
| Pricing | Free / OSS (MIT) |
| Capabilities | Read/Write — Claude runs the skill’s workflow locally (Bash/Python), not as an MCP tool |
| Verified | works · 2026-07-20 |
| Security | cleared · 2026-07-20 — provenance matches GPTomics/bioSkills, MIT, no advisories, read-only local pVACtools workflow |
How to install
bioSkills is not an npm package — skills are plain markdown/code read directly by the agent. Clone the repo, then either run the installer for the whole category or copy the single skill directory.
- Claude Code — clone and install via the bundled script:
git clone https://github.com/GPTomics/bioSkills cd bioSkills ./install-claude.sh --categories "immunoinformatics"The installer copies matching skills into
~/.claude/skills/(default target). Use./install-claude.sh --listto preview the skills first. - Claude Code / other agents — copy just this one skill:
cp -r bioSkills/immunoinformatics/neoantigen-prediction ~/.claude/skills/(run from inside your clone — the previous step left you in
bioSkills/; otherwise replacebioSkills/with the absolute path of your clone). The skill declares its external dependencies (pVACtools, VEP, HLA typers, LOHHLA) inSKILL.md; install them when prompted on first use.
What it does
Runs the full personalized-neoantigen discovery workflow with the pVACtools suite while enforcing the field’s downstream filters:
- pVACseq — translates somatic SNVs/indels into mutant peptides via VEP annotation (Wildtype + Frameshift plugins).
- pVACfuse — handles fusion-junction neoantigens.
- pVACbind — scores arbitrary peptides without a wild-type comparison.
- pVACview — manual re-tiering and candidate selection.
- Critical filters — HLA loss-of-heterozygosity (LOHHLA, the silent invalidator), clonal cancer cell fraction (CCF), agretopicity/foreignness quality, and expression thresholds.
The skill centers the predicted → presented → immunogenic validation tiers, stressing that most confidently-predicted strong binders are never presented, and most presented peptides never elicit a T-cell response.
Primary use cases: cancer vaccine target nomination, neoantigen ranking, checkpoint-response biomarker discovery.
Notes
Distributed as a SKILL.md (plus reference material) in the bioSkills collection — Claude executes the workflow locally via Bash/Python rather than as an MCP server. The upstream skill front-matter name is bio-immunoinformatics-neoantigen-prediction; if you invoke it as a namespaced plugin command it resolves under the bioSkills plugin, not as a bare /neoantigen-prediction. Binding-affinity detail is delegated to the mhc-binding-prediction skill and ranking to immunogenicity-scoring. pVACtools and its dependencies (VEP, HLA typers) require separate installation. Upstream directory: immunoinformatics/neoantigen-prediction.
Sources
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