Skills

Compute HEIM diversity and equity metrics from VCF or ancestry data.

Statistical fine-mapping of GWAS loci using SuSiE, SuSiE-inf, and Approximate Bayes Factors to identify credible sets and posterior inclusion probabilities…

Flow.bio API bridge — authenticate, browse pipelines/samples/projects, search, upload data, launch pipeline executions, and check run status on any Flow…

Federated variant lookup across 8 genomic databases — GWAS Catalog, Open Targets, PheWeb (UKB, FinnGen, BBJ), GTEx, and more.

Read-level validation of variant calls from any VCF, tumor/normal or tumor-only: counts read support in the BAMs (SNVs, indels, SV breakpoints), compares it…

Compute evidence-aware polygenic risk scores from a local VCF or WGS file through the validated just-prs engine and a pinned local just-prs MCP server.

Query and display Labstep electronic lab notebook data — experiments, protocols, resources, and inventory — via labstepPy.

Search PubMed and bioRxiv for bioinformatics literature, synthesise results into a structured report, and build a citation graph — all locally, with a…

Two-sample Mendelian Randomisation from GWAS summary statistics with IVW, MR-Egger, weighted median/mode, and full sensitivity analysis (Cochran Q, Egger…

Personalised nutrition report from consumer genetic data (23andMe, AncestryDNA, VCF) — interrogates nutritionally-relevant SNPs and generates actionable…

Interactive Goeminne proteomic aging clock with organ filters and per-protein contribution breakdown (protein NPX × coefficient).

Unified personal genomic profile report — reads a PatientProfile JSON and synthesizes all skill results into a single "Your Genomic Profile" document.

Gates polygenic risk score percentiles on trait applicability, score integrity and ancestry transferability, withholding the percentile when it would be…

Count rare, high-impact loss-of-function variants carried in a VCF, annotated with molecular consequence and population allele frequency

Analyse 10x Visium spatial transcriptomics: SpaceRanger outs or spatial h5ad in, then QC, Leiden clustering, Wilcoxon markers, Moran's I, neighbourhood…

Protein structure prediction with Boltz-2 (default) or OpenFold3.

Annotate VCF variants with Ensembl VEP REST, ClinVar significance, gnomAD/population frequency context, and prioritized variant ranking.

Annotate VCF variants with Ensembl VEP, ClinVar, and gnomAD.

Keep a Mac awake for a set duration or while a process runs.

Chromatic snapshot 변경의 원인, 실제 회귀 또는 flaky 여부를 조사할 때 사용한다.

Generate templated responses for common legal inquiries with escalation detection.

Lynx 컴포넌트의 문서·예제·런타임 결과를 환경별로 검증할 때 사용한다.

Show evidence-linked architecture, constraints and change scope, or review architecture improvement opportunities.

Searches the domestic courts of 122 jurisdictions — 153 databases, 49 automated — for extradition and arrest-warrant surrender decisions, each in its own…