deconvolute.default | R Documentation |
Devonvolute bulk RNA-seq data based on reference data
## Default S3 method:
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.
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