Thank you, Bastien! The first part of the answer was the one I expected ;) But I will try your suggestions!! Zitat von Bastien Chevreux <bach@xxxxxxxxxxxx>:
On Donnerstag 22 Juli 2010 Thomas Müller wrote:Is the number of rep_c I receive too high for a cDNA library?This question cannot be answered ... it's like: "Are there too many clouds in the sky?" Well, sometimes yes, sometimes no. Depends :-) But cannot be answered from afar.Have I made a mistake in the mira call (see below)? mira --project=nnn -job=denovo,454,est,normal --notraceinfo -SK:not=10 -AS:urd=no -OUT:rld=yes -AS:sd=no -CO:asir=yes 454_SETTINGS -LR:mxti=no -CL:qc=no -CL:cpat=no -AS:epoq=no -AL:mrs=90 -CO:rodirs=10 -SK:pr=80 -AS:mrl=50 -AL:mo=20 -FN:fai=nnn.fasta -FN:fqui=nnn.qualLooks pretty good. -CO:asir will lead to clustering of homologues/paralogues. In that case I would perhaps also try more stringent rules (-AL:mrs=95 - CO:rodirs=5), though this will lead to even more contigs. You may also be interested in trying miraSearchESTSNPs separately on each strain and use the results from step3 to do your analysis. Also try miraSearchESTSNPs with both strains at once :-) 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
-- Thomas Müller Crop Plant Biodiversity and Breeding Informatics Group (350b) Institute of Plant Breeding, Seed Science and Population Genetics University of Hohenheim Fruwirthstrasse 21 D-70599 Stuttgart Phone: +49-711-459 24293 -- 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