Entering edit mode
4.3 years ago
r_mvl
▴
50
Hello!
I am working with RNA-seq data, from paired end sequencing (10x precisely, and sequenced on a NextSeq platform).
Basically I have a list of sequences (15 bp long) which are present in only a subset of my R1 reads. What I would like to do is to filter the R2 reads which match this criteria. Do you know how I could achieve this?
Many thanks for your help.
Please give a representative example of input and expected output. R1 in 10X are barcodes and UMIs which are not present in R2. It is not clear what you aim to do.