Hi Pierre Lindenbaum, I’ve installed jvarkit and tested it on my data. However, I can't quite understand the output, specially regarding how to determine the genomic coordinates for the read SRR73.14 and the specific part of the sequence it has mapped to.
#Read-Name Flag MAPQ CHROM READ-POS0 READ-BASE READ-QUAL REF-POS1 REF-BASE CIGAR-OP
SRR73.14 0 0 chr1 0 C * 9999 N S
SRR73.14 0 0 chr1 1 T + 10000 N S
SRR73.14 0 0 chr1 2 A + 10001 N S
SRR73.14 0 0 chr1 3 A # 10002 N M
SRR73.14 0 0 chr1 4 A % 10003 N M
SRR73.14 0 0 chr1 5 C % 10004 N M
SRR73.14 0 0 chr1 6 C ( 10005 N M
SRR73.14 0 0 chr1 7 C + 10006 N M
SRR73.14 0 0 chr1 8 T ' 10007 N M
If you are blasting your sequences you can export your results in CSV format. There you will have these metrics.
Hi, I'm working with aligments obtained with pbmm2, minimap2 and ngmlr. I would like to obtain similar results to those generated by BLAST. I'm looking for ways to extract the target positions that have aligned.