Data

Use when sending local changes back to the project (an added journal profile, a fixed checklist item, an adapted skill) or reporting a false positive or bug.

Use when clinical data may contain PHI and must be de-identified before any LLM-assisted analysis.

Use when designing a study that benchmarks AI systems against a human-expert panel, before data collection.

Use when a tabular dataset (CSV, Excel, Parquet, Stata, SAS) needs a data dictionary.

Use when preparing a medical-imaging dataset (DICOM/NIfTI) for modelling.

Use when a trained medical-imaging model needs its documentation.

Use when you must prove an analysis ran on the intended data or lock a dataset version.

Use when drafting a medical research manuscript or any IMRAD section.

Analyze a Figma file via the Figma REST API and generate an interactive design knowledge graph (pages, screens, components, component sets, instances, design…

Local Scanpy pipeline for single-cell RNA-seq QC, optional doublet detection, clustering, marker discovery, optional CellTypist annotation, optional latent…

Design and build complete web experiences from scratch — award-level product and marketing pages, cinematic scroll-directed sites where the page is directed…

Use when data needs statistical analysis.

Analyze a user's Plannotator plan archive to extract denial patterns, feedback taxonomy, evolution over time, and actionable prompt improvements — then…

Route and coordinate an end-to-end design-award workflow across winner research, evidence-based evaluation, award matching, entry-text preparation, and final…

Automated sequencing quality control and advanced visualization wrapping FastQC, MultiQC, and custom chart generation.

Extract numerical data from scientific figure images using Claude vision + OpenCV calibration.

Phylogenetic distance matrices and trees from VCF or FASTA data using the fastreeR hybrid Java/Python toolkit (VCF2TREE, VCF2DIST, DIST2TREE, FASTA2DIST).

Predict gene and transcript structure (intervals, exons, strand) from a DNA sequence using the Genomic Intelligence DNA Annotation model, via the hosted…

End-to-end GWAS automation wrapping PLINK2 for genotype QC and REGENIE for two-step whole-genome regression association testing.

Differential expression analysis for label-free quantitative (LFQ) intensity data with standard MaxQuant and DIA-NN output.

NGS read QC, alignment, and BAM processing pipeline.

Semantic search across UK Biobank's 12,000+ data fields and publications — find the right variables for your research question.

High-performance data analysis using Polars - load, transform, aggregate, visualize and export tabular data.

Turn a one-line description of a repetitive task into a reusable, self-guarding slash command.