On Mon, Mar 23, 2015 at 7:02 PM, lenis vasilis <val1@xxxxxxxxxx> wrote: > Hi Peter, > > Thank you very much for the script but I have some problems when I'm running > it. > When I run it with the sample that I sent you it runs smoothly, both for > padded and unpadded. > > When I run it with the other sample (the sample that I had problem with > Mira_convert in Mira's previous version, and I solved it with your > exhortation to run it in a newer version). > > Here is the std output: > > [maf2sam] NOTE: Producing SAM using a gapped reference sequence. > [maf2sam] Identified as MIRA v3.9 or later (MAF v2) > [maf2sam] WARNING - Support for this is *still* EXPERIMENTAL! > [maf2sam] Identified 3 read groups > [maf2sam] Starting main pass though the MAF file > [maf2sam] Unpaired read chrM > [maf2sam] Almost done, 436 orphaned paired reads remain > Traceback (most recent call last): > File "./maf2sam.py", line 781, in <module> > print current_read > File "./maf2sam.py", line 239, in __str__ > raise ValueError("%s vs %i for %s" % (cigar, len(read_seq_unpadded), > read_seq)) > ValueError: 17S59M26S vs 101 for > TTCCT*CATGACACATAGTTAATGTAGCTTAAAATTAAAGCAAGGCACTGAAAATGCCTAGATGAGTATATTAACTACATAAACATATAGGTTTTGGTCCCA > > Thank you very much, > Vasilis. I think my script is getting confused by the * (gap) within the soft-clipped part of the read. I am guessing that MIRA did some trimming after some alignment process had inserted the gap. Perhaps I simply didn't have a broad enough set of test data before? Could you send me this MAF file by dropbox too? Thanks, Peter -- 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