Hello
I have paired end sequences for 6 subjects. For each subject, read group information should be added in the bam file?. Read group info is different from subject to subject, right? If so, why combine all the forward fastq files as given in the above code. I am trying to understand the GATK pipeline for NGS analysis. Sorry for the silly question
Making a vague reference to a previous post does not help you or us. Please provide a link for that post.
Sorry, have given the link above.
Since you are interested in running
bwa-mem2you will need to make the necessary changes inside the script to replace the command but otherwise you can use the answer bwa mem: Passing a variable to read group to run the script as shown.bwa-mapper.sh read_1.fq.gz read_2.fq.gz. Your read headers will need to follow the standard illumina format.Thread continues: Read group info