Single Cell

A comprehensive documentation skill for scvi-tools, a Python framework for probabilistic deep generative models in single-cell genomics. It provides guidance on models for RNA-seq, ATAC-seq, multimodal data integration, spatial transcriptomics, and specialized modalities like methylation and cytometry analysis.

This skill provides a comprehensive toolkit for analyzing single-cell RNA-seq data using the scanpy library. It enables quality control, normalization, dimensionality reduction (PCA/UMAP/t-SNE), clustering, marker gene identification, cell type annotation, and publication-quality visualizations.

This skill provides comprehensive guidance for programmatically accessing the CZ CELLxGENE Census, a collection of 61+ million single-cell genomics data. It covers querying expression data by cell type, tissue, or disease, integrating with PyTorch for machine learning, and using scanpy for analysis workflows.

This skill provides comprehensive documentation and reference material for working with AnnData, a Python package for handling annotated data matrices used in single-cell genomics. It covers creating, reading, writing, and manipulating AnnData objects, along with best practices for memory management and integration with the scverse ecosystem (Scanpy, Muon, PyTorch).

This skill should be used when working with LaminDB, an open-source data framework for biology that makes data queryable, traceable, reproducible, and FAIR. Use when managing biological datasets (scRNA-seq, spatial, flow cytometry, etc.), tracking computational workflows, curating and validating data with biological ontologies, building data lakehouses, or ensuring data lineage and reproducibility in biological research. Covers data management, annotation, ontologies (genes, cell types, diseases, tissues), schema validation, integrations with workflow managers (Nextflow, Snakemake) and MLOps platforms (W&B, MLflow), and deployment strategies.

This skill should be used when working with genomic interval data (BED files) for machine learning tasks. Use for training region embeddings (Region2Vec, BEDspace), single-cell ATAC-seq analysis (scEmbed), building consensus peaks (universes), or any ML-based analysis of genomic regions. Applies to BED file collections, scATAC-seq data, chromatin accessibility datasets, and region-based genomic feature learning.

Infer gene regulatory networks (GRNs) from gene expression data using scalable algorithms (GRNBoost2, GENIE3). Use when analyzing transcriptomics data (bulk RNA-seq, single-cell RNA-seq) to identify transcription factor-target gene relationships and regulatory interactions. Supports distributed computation for large-scale datasets.