Ross ROSS = Recommend OSS · open-source software intelligence for agents

satijalab/seurat

R toolkit for single cell genomics observed · 2026-08-28

github.com/satijalab/seurat · homepage · R · NOASSERTION (other) observed · 2026-08-28

Health v2 · maintenance only

92/100

  • Activity 99
  • Release rhythm 78
  • Longevity 100

Flags: no_license

How is this computed?

round(0.45*activity + 0.35*rhythm + 0.20*longevity); archived -> min(score, 10) — computed 2026-09-02. Adoption (stars, forks) is never an input.

  • gap_med: 76.5
  • age_days: 4123
  • days_rel: 68
  • days_push: 8
  • n_releases_24m: 7

Full methodology

Adoption not part of the score

2790 stars · 995 forks observed · 2026-08-28

What it is AI-extracted, prompt v1, taxonomy v1, 2026-08-30, confidence not recorded

Seurat is an R toolkit for single-cell genomics developed by the Satija Lab, providing a complete pipeline for analyzing single-cell RNA-seq, multimodal, and spatially-resolved transcriptomics data. Version 5 adds scalable analysis methods, cross-modality integration via bridge integration, sketch-based workflows for millions of cells, and spatial dataset support.

Use cases

  • analyze single-cell rna-seq data in r
  • cluster and visualize single cell gene expression
  • integrate scrna-seq and scatac-seq datasets
  • analyze spatial transcriptomics data like visium
  • run differential expression on single cell clusters
  • map query cells onto a multimodal reference atlas
  • scale single cell analysis to millions of cells
  • demultiplex hashed samples with hashtag oligos

When to choose

  • you work in R and need a mature, well-documented single-cell analysis pipeline
  • you need multimodal or cross-modality integration (RNA + ATAC, protein, spatial)
  • you need to analyze very large datasets with sketch-based or on-disk (BPCells) workflows
  • you want extensive tutorials, vignettes, and an active community for scRNA-seq analysis

When to avoid

  • you need a Python-based single-cell workflow (consider Scanpy instead)
  • you need raw sequencing processing or alignment rather than downstream analysis
  • you need a non-genomics data analysis toolkit
  • you cannot install R (version 4.0+) or its compiled dependencies

Facets

library · maturity stable

data-science machine-learning data-visualization nlp bioinformatics data-science machine-learning windows single-cell-genomics scrna-seq spatial-transcriptomics multimodal-analysis data-integration clustering dimensionality-reduction differential-expression r-package cran bioconductor-adjacent human-cell-atlas scatac-seq reference-mapping sketch-based-analysis macos linux r

5 sources

Member repositories

RepositoryRoleHealth v2
satijalab/seuratmain92

For agents

markdown · JSON · MCP: product_card(name="satijalab/seurat")

Data as of 2026-08-30T08:39:29.467469+00:00 · Report a problem