AnnData on-disk workflows for large single-cell and spatial omics datasets using .h5ad and Zarr stores. Covers memory-aware reading with backed mode, lazy access with anndata.experimental.read_lazy, d
Use with AI
Install the MCP server or CLI to instantly fetch AnnData on disk documentation:
Install command
claude mcp add biocontext7 -- npx @biocontext7/mcpOr share this page: biocontext7.com/tools/anndata-on-disk
cellSNP-lite — fast C-based tool for genotyping single cells and bulk samples at known or de-novo SNP sites from BAM/SAM files. Generates sparse genotype matrices (AD/DP/OTH counts) in VCF/BCF format
1 shared topic • 2 shared operations
Docker — container platform for building, running, and distributing reproducible bioinformatics environments. Provides Dockerfile authoring, image management, container execution with volume mounts fo
1 shared topic • 2 shared operations
FLAMES — Full-Length Analysis of Mutations and Splicing for bulk and single-cell long-read RNA-seq data. R/Bioconductor pipeline for barcode demultiplexing, isoform discovery, transcript quantificatio
1 shared topic • 2 shared operations
Data-driven computational pipeline framework enabling scalable and reproducible scientific workflows using software containers.
1 shared topic • 2 shared operations
Vireo (vireoSNP) is a Bayesian variational inference tool for donor demultiplexing in pooled single-cell RNA-seq and single-cell ATAC-seq experiments. It assigns cells to donors using SNP genotype inf
1 shared topic • 2 shared operations