deconvolute.RdDevonvolute bulk RNA-seq data based on reference data
# S3 method for default deconvolute( expr_mat, genes_use, reference = "ABA", stage = "E13", annotation_level = "custom_2", pseudo_tpm = FALSE, other_types = FALSE, involve_regions = NULL ) deconvolute(object, ...)
| expr_mat | Expression matrix to deconvolute. |
|---|---|
| genes_use | Marker genes to use for deconvolution. |
| reference | Which reference to use. |
| stage | Developmental stage to use as reference. |
| other_types | Whether to infer proportions of type 'other'. |
A tibble with deconvoluted proportions for each reference structure.