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Deep probabilistic analysis of single-cell and spatial omics data
Infer copy number variation (CNV) from scRNA-seq data. Plays nicely with Scanpy.
Rapids_singlecell: A GPU-accelerated tool for scRNA analysis. Offers seamless scverse compatibility for efficient single-cell data processing and analysis.
A single cell transcriptomics pipeline for QC, integration and making the data presentable
Tutorials for multimodal omics data analysis
Download and Convert METASPACE datasets to common formats such as AnnData or SpatialData
Feature-rich Python implementation of the tximport package for gene count estimation.
Awesome GRN enhanced AnnData toolkit