Hi All
I have a mate paired reads (facing outwards) with highly variable insert size. Any aligner that will allow me to map these reads as well as pair them up.
Also I should mention the length of read 1/2 in my case are not equal due to linker cleaning step which will remove linker sequence from the read and it can be found at any random position in the read.
Best, -Abhi
@SES : data is for cDNA but the read length after trimming is < 80 bp which is significantly smaller than the exon size. I dont see an issue as most of the reads should map within an exon and only a small chunk should come from exon-exon boundaries.