> On Aug 14, 2011, at 18:34 , Nestor Zaburannyi wrote: >> I have one Paired-end solexa file in which sequences /1 and /2 are expected >> to overlap by approx. 50 bases. I tried to use "fastq-join" ( >> http://code.google.com/p/ea-utils/wiki/FastqJoin ), but i am not satisfied >> with results. Can MIRA handle "negative" inserts sizes? I think it will >> perform much better than standalone tools. Just a thought. > MIRA oes not work with "insert sizes" per se, but with "template insert > sizes". It stems from the old Sanger sequencing days when pieces of DNA > (templates) were inserted into sequencing vectors to be sequenced. > As such, the "template insert size" does not define the distance which > separates two reads, but the expected size of a DNA template and therefore > the distance which separates the outer ends of two reads. As result to this, > the size cannot get below zero. Got it. > For what you want to do, MIRA will be perfectly happy if you set the minimum > size to 0. Not quite understood. Why 0? If my reads are 2 x 120 and they overlap by 50 bases, then the average insert should be 2 x 120 - 50 = 190 bp. With 0.3 deviation it should be, for example: -GE:tismin=130:tismax=250 MIRA will do what i want? Sincerely yours Nestor -- You have received this mail because you are subscribed to the mira_talk mailing list. For information on how to subscribe or unsubscribe, please visit http://www.chevreux.org/mira_mailinglists.html