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Hi I have list of 10X SingleCell data which R1 are missing from fastq files,
is there any way than we can align the R2 only using star and then feed bam file to monopogen germline
Thanks
should I use specific parameters during alignment /monopogen
Thanks
The text was updated successfully, but these errors were encountered:
Monopogen is highly flexible regarding read alignment. I believe you can proceed with that, but please ensure that the cell barcode is included in your aligned BAM files (with the CB flag).
Hi I have list of 10X SingleCell data which R1 are missing from fastq files,
is there any way than we can align the R2 only using star and then feed bam file to monopogen germline
Thanks
should I use specific parameters during alignment /monopogen
Thanks
The text was updated successfully, but these errors were encountered: