Hi!
I am using cellranger arc 2.0 and need to use the .possorted.bam files for allelic quantification and wanted to remove PCR duplicate reads. For the gex_possorted_bam.bam I have a doubt regarding UMI: I understood that reads coming from the same UMI barcode and cell barcode and mapping to the same gene are counted only once in the count matrix, but I did not understand if the BAM file is already filtered for duplicated reads with same cell and molecule barcode and mapping to the same position. If not, how do I filter it?
Thank you!!
Hi! I am using cellranger arc 2.0 and need to use the .possorted.bam files for allelic quantification and wanted to remove PCR duplicate reads. For the gex_possorted_bam.bam I have a doubt regarding UMI: I understood that reads coming from the same UMI barcode and cell barcode and mapping to the same gene are counted only once in the count matrix, but I did not understand if the BAM file is already filtered for duplicated reads with same cell and molecule barcode and mapping to the same position. If not, how do I filter it? Thank you!!
Paola