On 04 Feb 2014, at 19:29 , Adrian Pelin <apelin20@xxxxxxxxx> wrote: > I am attaching a figure with obtained results. On the left I have the PCR > clones that I sequenced, the number in parenthesis is the number of clones > that had that specific haplotype. On the right I have 2 mira haplotypes > produced from small contigs, smaller than 1.5kb. As you can see the second > one is fine, it is the same 2nd one from the left figure. The first one made > by mira however, seems to be a combination between #3, than #4 or #5 and than > #1. It’s not only highly polymorphic, the naming of the contig also suggests it is highly repetitive. This is always a problem, and in repeats all MIRA can give is a best guess as there is really no good way to ensure that more distantly occurring "SNP-loci” really belong together. > […] > Would be very neat if MIRA could build variants and their respective > frequencies for highly polymorphic loci. In case you have Illumina data, you might try a couple of dirty tricks to improve things (but this might also worsen the results): extract the reads from the assembled contigs, reassemble them with highly stringent parameters like -AL:mrs=95 -CO:rodirs=1 … maybe that’ll work. B. -- 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