Skill UI

AnnData supplies a Python-native container for annotated matrices, letting researchers store measurements alongside rich metadata, read/write h5ad/zarr/loom/10X files, and integrate with the scverse tools when building single-cell or related data workflows.

PyDESeq2 brings the DESeq2 differential expression workflow to Python, letting users load bulk RNA-seq counts, specify design formulas, fit DESeq2 models, run Wald tests with FDR correction, optionally apply apeGLM shrinkage, and export gene-level statistics within pandas/AnnData pipelines.

AnnData supplies a Python-native container for annotated matrices, letting researchers store measurements alongside rich metadata, read/write h5ad/zarr/loom/10X files, and integrate with the scverse tools when building single-cell or related data workflows.

PyDESeq2 brings the DESeq2 differential expression workflow to Python, letting users load bulk RNA-seq counts, specify design formulas, fit DESeq2 models, run Wald tests with FDR correction, optionally apply apeGLM shrinkage, and export gene-level statistics within pandas/AnnData pipelines.

Scanpy is a comprehensive Python toolkit built on AnnData for analyzing single-cell RNA-seq datasets. It provides a complete, scalable workflow covering every stage of single-cell genomics analysis, including quality control (QC), normalization, dimensionality reduction (PCA, UMAP, t-SNE), cell clustering, marker gene identification, and cell type annotation. Ideal for researchers generating publication-quality single-cell visualizations and performing exploratory analysis.