AI prompts.
Agent skills.

Rich downstream visualisation and reporting for bulk RNA-seq differential expression and scRNA marker/contrast

Import DRAGEN-exported Illumina result bundles into ClawBio for local tertiary analysis and downstream routing.

Compute epigenetic age from DNA methylation arrays using PyAging clocks from GEO accessions or local files.

Local scVI/scANVI-based single-cell latent embedding and batch-aware integration from raw-count .h5ad or 10x

Aggregates QC reports from any bioinformatics tool outputs (FastQC, fastp, STAR, Picard, samtools, etc.) into

Two-sample Mendelian Randomisation from GWAS summary statistics with IVW, MR-Egger, weighted median/mode, and

Annotate VCF variants with Ensembl VEP, ClinVar, and gnomAD. Ranks variants by impact (HIGH/MODERATE/LOW/MODIFIER) and generates a reproducible report.

Fetch a region of GWAS summary statistics from the NHGRI-EBI GWAS Catalog harmonised collection via tabix-on-FTP. Use when an agent needs GWAS beta / SE / p-value for every variant in a window for one specific study (GCST accession). Input: accession, chromosome, start, end. Output: harmonised TS...

Medical biostatistics hypothesis testing toolkit: t-tests, ANOVA, chi-square, Fisher exact, Mann-Whitney, Kruskal-Wallis, sample size calculation, power analysis, multiple testing correction, survival analysis, and clinical trial biostatistics.

Evidence-grounded target validation scoring with GO/NO-GO decisions for drug discovery campaigns

Multi-agent system for biomedical literature review and synthesis

Local Scanpy pipeline for single-cell RNA-seq QC, optional doublet detection, clustering, marker discovery, optional CellTypist annotation, optional latent downstream mode from integrated.h5ad/X_scvi, and optional two-group contrastive marker analysis from raw-count .h5ad or 10x Matrix Market input.