Hi all,
I have encountered a problem with soap2, when I would like to map my 17-30nt reads to genome (both fasta).
I used default parameters and soap2 output was
"length y <0 skip anyway"
with only some 28-30nt reads mapped successfully.
Is it possible to adjust the paramenters for mapping all the reads?
Thank you!
Franklin
I have encountered a problem with soap2, when I would like to map my 17-30nt reads to genome (both fasta).
I used default parameters and soap2 output was
"length y <0 skip anyway"
with only some 28-30nt reads mapped successfully.
Is it possible to adjust the paramenters for mapping all the reads?
Thank you!
Franklin
Comment