On Donnerstag 18 März 2010 Martin A. Hansen wrote: > I have 2M 454 titanium reads (~500bp in length). GC content is 65% (!) and > genome size is 7Mb. > > I have a fairly good assembly done with Newbler: > [...] > So I wanted to do an assembly with Mira to compare the assemblies. I > followed the Mira 454 tutorial (sff_extract and remembering to include > quality and traceinfo!) and simply ran with the following options: > [...] > But the result is disappointing: > So, any suggestions? I suppose the standard config does not cope very well with high coverages as you have (~100x), it's is geared towards more 'normal' coverage. I suppose that this together with the high GC will lead to many false positive repeats detected. Hmmm ... could you please try adding 454_SETTINGS -CO:mrpg=20 and tell whether this improves the assembly? Regards, Bastien -- 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