I have scRNAseq data (counts files not fastq files). I got 3 types of counts including:
1- BarcodeCounts 2- ReadCounts 3- TranscriptCounts
now I want to do differentially expression analysis to identify DE genes. for normal RNAseq we ususally use read counts to identify significant genes. do you know which of these files must be used for single cell RNAseq for DE analysis?