Tools

Scanpy Preprocess

Standard single-cell RNA-seq preprocessing: filter cells by gene count, filter genes by cell count, normalize, log transform, identify highly variable genes. Essential first step before UMAP and clustering.

Runnablesequencing readsscverse/scanpy | 2,497 stars

Catalog entry

About this entry

Standard single-cell RNA-seq preprocessing: filter cells by gene count, filter genes by cell count, normalize, log transform, identify highly variable genes. Essential first step before UMAP and clustering.

CategoryTools
StatusRunnable
Inputsequencing reads
OutputResults ready for review

Use in DarwinOmics

How to use it

Use this tool to reproduce a concrete analysis step from supplied inputs, captured parameters, and versioned outputs, then compare the regenerated artifacts against the submitted result record.