目录
- .githubUpdate release_checks.yaml4个月前
- REdits to handle HTO demux when HTO assay is a subset of RNA, combines previous fixes with new average expression8天前
- dataFinalize SeuratObject split5年前
- instAdd citatation for Seuratv52年前
- manUpdate documentation4天前
- srcRemove redundant exception handling in RModularityOptimizer21天前
- testsAdd test for BPCells FindAllMarkers w/ col-major storage7天前
- vignettesUpdate vignettes to avoid errors with slot instead of layer4个月前
- .RbuildignoreDrop appveyor.yml from .Rbuildignore1年前
- .gitattributesDevelopment version of Seurat8年前
- .gitignoreadd other main pages5年前
- CODE_OF_CONDUCT.mdUpdate CODE_OF_CONDUCT.md6年前
- DESCRIPTIONBump version3天前
- LICENSEUpdate license4年前
- LICENSE.mdUpdate license4年前
- NAMESPACEUpdate documentation9天前
- NEWS.mdUpdate changelog4个月前
- README.mdDrop AppVeyor badge from README1年前
- _pkgdown.yamlAdd missing topics to _pkgdown.yaml1年前
- cran-comments.mdUpdate cran-comments.md4个月前
- index.mdupdated docs to match website versions2年前
- seurat.RprojAdd the Rproj file5年前
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Seurat v5
Seurat is an R toolkit for single cell genomics, developed and maintained by the Satija Lab at NYGC.
We are excited to release Seurat v5! This updates introduces new functionality for spatial, multimodal, and scalable single-cell analysis.
Seurat v5 is backwards-compatible with previous versions, so that users will continue to be able to re-run existing workflows.
Instructions, documentation, and tutorials can be found at:
Seurat is also hosted on GitHub, you can view and clone the repository at
Seurat has been successfully installed on Mac OS X, Linux, and Windows, using the devtools package to install directly from GitHub
Improvements and new features will be added on a regular basis, please post on the github page with any questions or if you would like to contribute
For a version history/changelog, please see the NEWS file.