Closed MichaelPeibo closed 4 years ago
Hi @chris-mcginnis-ucsf ,
Thanks for developing this great package.
I am trying to understand the preprocessing step. In MULTIseq.Align.Suite.R code, there is step called Remove reads representing duplicated UMIs on a cell-by-cell basis https://github.com/chris-mcginnis-ucsf/MULTI-seq/blob/73411337bc470b846c12f201f96699ae5e1188be/R/MULTIseq.Align.Suite.R#L50-L52
MULTIseq.Align.Suite.R
Remove reads representing duplicated UMIs on a cell-by-cell basis
I did not get through with it. 1.This duplicated UMIs is detected in same Cell?
Or maybe I did not understand the code.
Thanks!
I think I figure this out. Length of different and unique UMIs(no matter how many reads of one kind of UMI) are counts for certain barcode.
Hi @chris-mcginnis-ucsf ,
Thanks for developing this great package.
I am trying to understand the preprocessing step. In
MULTIseq.Align.Suite.R
code, there is step calledRemove reads representing duplicated UMIs on a cell-by-cell basis
https://github.com/chris-mcginnis-ucsf/MULTI-seq/blob/73411337bc470b846c12f201f96699ae5e1188be/R/MULTIseq.Align.Suite.R#L50-L52I did not get through with it. 1.This duplicated UMIs is detected in same Cell?
Or maybe I did not understand the code.
Thanks!