Hi,
After reading the tutorials carefully, I still feel confused how to prepare the input data. In most cases, users want to get cell-type fractions from tumor bulk RNA-seq data using the 10X data as reference. On the website, the author declared seting datatype='counts', so is sc_ref the UMI matrix of 10X data? For bulkdata, should we use counts, TPM or FPKM data?
Could you please give an example on the usage website? For instance, deconvolution of bulk PBMC dataset with 10X single-cell PMBC data.