Closed dawnmy closed 1 year ago
I noticed that sometimes, MA produces SAM file with the same alignment occurring multiple times on Nanopore data. They have the same read, ref contig, start pos, and even the cigar. The command line I used:
maCMD -t 20 -x ma_db.json -p Nanopore -i barcode01.fq.gz -o barcode01.sam -s maxSpan -M 5 --Use_M_in_CIGAR false
One of the read have six the same alignment (only show read, ref_contig, pos):
read
ref_contig
pos
185-b77e-25cb88888888 GCF_000182965.3|NC_032094.1 171367 185-b77e-25cb88888888 GCF_000182965.3|NC_032094.1 171367 185-b77e-25cb88888888 GCF_000182965.3|NC_032094.1 171367 185-b77e-25cb88888888 GCF_000182965.3|NC_032094.1 171367 185-b77e-25cb88888888 GCF_000182965.3|NC_032094.1 171367 185-b77e-25cb88888888 GCF_000182965.3|NC_032094.1 171367
I am using Version 1.1.4-d2d8fc1-0 installed with conda
Version 1.1.4-d2d8fc1-0
Is this expected. What could be the reason causing this issue?
My bad, there are some duplicate sequences in the ref db.
I noticed that sometimes, MA produces SAM file with the same alignment occurring multiple times on Nanopore data. They have the same read, ref contig, start pos, and even the cigar. The command line I used:
One of the read have six the same alignment (only show
read
,ref_contig
,pos
):I am using
Version 1.1.4-d2d8fc1-0
installed with condaIs this expected. What could be the reason causing this issue?