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      /\ \         /\ \ /\ \     /\_\      / /\
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      /\__ \     / /\ \ \\ \ \_/ / /     / / /\ \__
     / /_ \ \   / / /\ \ \\ \___/ /     / / /\ \___\
    / / /\ \ \ / / /  \ \_\\ \ \_/      \ \ \ \/___/
   / / /  \/_// / /   / / / \ \ \        \ \ \
  / / /      / / /   / / /   \ \ \   _    \ \ \
 / / /      / / /___/ / /     \ \ \ /_/\__/ / /
/_/ /      / / /____\/ /       \ \_\\ \/___/ /
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r-scgate 1.6.2
Propagated dependencies: r-biocparallel@1.38.0 r-dplyr@1.1.4 r-ggplot2@3.5.1 r-ggridges@0.5.6 r-patchwork@1.2.0 r-reshape2@1.4.4 r-seurat@5.1.0 r-ucell@2.8.0
Channel: guix
Location: gnu/packages/bioconductor.scm (gnu packages bioconductor)
Home page: https://github.com/carmonalab/scGate
Licenses: GPL 3
Synopsis: Marker-based cell type purification for single-cell sequencing data
Description:

This package provides a method to purify a cell type or cell population of interest from heterogeneous datasets. scGate package automatizes marker-based purification of specific cell populations, without requiring training data or reference gene expression profiles. scGate takes as input a gene expression matrix stored in a Seurat object and a GM, consisting of a set of marker genes that define the cell population of interest. It evaluates the strength of signature marker expression in each cell using the rank-based method UCell, and then performs kNN smoothing by calculating the mean UCell score across neighboring cells. kNN-smoothing aims at compensating for the large degree of sparsity in scRNAseq data. Finally, a universal threshold over kNN-smoothed signature scores is applied in binary decision trees generated from the user-provided gating model, to annotate cells as either “pure” or “impure”, with respect to the cell population of interest.

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