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Seurat is an open-source R toolkit for single-cell genomics data analysis, enabling visualization, clustering, differential expression, and data integration across scRNA-seq, scATAC-seq, and multimodal datasets. The v5 release adds bridge (cross-modality) integration, scalable sketch-based analysis for millions of cells, and high-performance backends like BPCells. It also supports spatial transcriptomics analysis and reference mapping (Azimuth) for annotating and translating query datasets while remaining backward compatible with earlier versions.
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Excerpts where Seurat appeared in the AI's answer

Seurat : Developed by the Satija Lab in R, Seurat is arguably the most widely used toolkit for scRNA-seq QC, analysis, and integration.

Seurat (R): The most widely adopted R toolkit for single-cell genomics.