We are mapping some RNA-seq data to the hg19 reference genome sequence. We used blat, which allows 750,000 as the intron size in default, but it was a little slow possibly due to the lack of multithread supporting, 3 days for 1.5 million reads. We have found some other softwares which handle small gap/indel, but such gap/indel are usually too small compared to the intron size. We wonder if there is any other software for alignment over large gaps. Thank you.
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Thank you for the suggestions. I thought tophat used bowtie to map reads to existing known transcriptome, didn't know it could also uncover unknown transcript isoforms.Originally posted by Thomas Doktor View PostI would suggest using TopHat: http://tophat.cbcb.umd.edu/
Quoted from tophat manual, "Currently, TopHat does not allow short (fewer than a few nucleotides) insertions and deletions in the alignments it reports."
I get it now. It splits the read, and align them individually first. I will try it.Last edited by superligang; 04-10-2010, 01:27 AM.
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Maybe, when published, "phaster" will do a good job at it. You may want to ask Phil Green (phrap, cross_match) for "phaster" beta-testing; it is doing a pretty fast gapped alignment. You may also try to use 'cross_match' which is also capable of doing gapped alignments.
cheers,
Sven
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