@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.
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
2 answers
I've had decent luck with Novoalign for mate pair data. The mate pair data sets I've worked with have had significant contamination by paired-end reads (innies) and Novoalign has built in logic to deal with those pairs:
http://www.novocraft.com/wiki/tiki-index.php?page=Paired+Read+Modes
I haven't personally used Stampy but I hear that it can also work well.
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