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Identify singlets, doublets and negative cells from multiplexing experiments. Annotate singlets by tags.
MULTIseqDemux( object, assay = "HTO", quantile = 0.7, autoThresh = FALSE, maxiter = 5, qrange = seq(from = 0.1, to = 0.9, by = 0.05), verbose = TRUE )
A Seurat object with demultiplexing results stored at object$MULTI_ID
object$MULTI_ID
Seurat object. Assumes that the specified assay data has been added
Name of the multiplexing assay (HTO by default)
The quantile to use for classification
Whether to perform automated threshold finding to define the best quantile. Default is FALSE
Maximum number of iterations if autoThresh = TRUE. Default is 5
A range of possible quantile values to try if autoThresh = TRUE
Prints the output
https://www.biorxiv.org/content/10.1101/387241v1
if (FALSE) { object <- MULTIseqDemux(object) }
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