Hi I have never used BWA before and so was wondering if anyone knows how I can use BWA to map my reads to my reference genome. My data is as follows:
L001_R1.fasta
L001_R2.fasta
L002_R1.fasta
L002_R2.fasta
etc
There are 12 files in total and as you can see they are paired reads.
So does anyone have any idea?
Any help would be much appreciated.
Thanks,
Tom
L001_R1.fasta
L001_R2.fasta
L002_R1.fasta
L002_R2.fasta
etc
There are 12 files in total and as you can see they are paired reads.
So does anyone have any idea?
Any help would be much appreciated.
Thanks,
Tom
Comment