Provides a number of utility functions for handling single-cell (RNA-seq) data from droplet technologies such as 10X Genomics. This includes data loading from count matrices or molecule information files, identification of cells from empty droplets, removal of barcode-swapped pseudo-cells, and downsampling of the count matrix.
|Bioconductor views||Coverage DataImport GeneExpression ImmunoOncology RNASeq Sequencing SingleCell Transcriptomics|
|Package repository||View on GitHub|
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