Entering edit mode
3.8 years ago
vinayjrao
▴
250
Hi,
I am working with some whole exome data, which was received as cram files. I am facing some problems converting the cram
files to either bam
or fastq
. I would like to know if anyone has tried to remove duplicates and call variants from the cram file. I am certainly going to give this a shot regardless, but I would like to be careful of any intricate changes that need to be made in order to achieve this.
Thanks in advance