Unified biological database evidence owner. Use for gene annotation, variant clinical significance, cancer mutation evidence, GWAS trait associations, pathway mapping, target-disease evidence, protein structures, protein interaction networks, reference single-cell census queries, and cross-database biological ID mapping. Do not use for full single-cell analysis, bulk RNA-seq differential expression, BAM/VCF processing, protein embedding models, metabolic flux modeling, genomic interval ML, or flow-cytometry file parsing.
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Low
Low-risk findings worth noting
Low
Low-risk findings.
1 low severity finding. Worth noting, but not necessarily harmful.
The skill exposes the agent to untrusted, user-generated content from public third-party sources, creating a risk of indirect prompt injection. This includes browsing arbitrary URLs, reading social media posts or forum comments, and analyzing content from unknown websites.
The required workflow is evidence gathering from biological data sources listed in SKILL.md/references, and since those sources at runtime are external (e.g., Ensembl/NCBI/ClinVar/GWAS/Reactome/Open Targets/STRING/AlphaFold/CELLxGENE), their fetched results would be outside-authored prose fed into the LLM context via the tool/API response, creating an indirect prompt-injection exposure path.
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