Dear all!
Now I have statistics from all my runs (Pair and SNPs). Can I see all my reads in base pair (nucleotide sequences of ol my reads)? Does I need another program for that, for example BWA?
And another question: Can I to change limits of coverage, when I create snps.txt and snps_sorted.txt files in SNP PipeLine?
Thanks,
Artem
Now I have statistics from all my runs (Pair and SNPs). Can I see all my reads in base pair (nucleotide sequences of ol my reads)? Does I need another program for that, for example BWA?
And another question: Can I to change limits of coverage, when I create snps.txt and snps_sorted.txt files in SNP PipeLine?
Thanks,
Artem