[mira_talk] Re: Assembly genome pine
- From: Rocío Bautista <rociobm@xxxxxxxxxxx>
- To: mira_talk@xxxxxxxxxxxxx
- Date: Tue, 25 Nov 2008 09:07:53 +0100
Bastien Chevreux escribió:
Ummm ... why are you setting a minimum read length of "3" for Sanger reads if
you do only a 454 assembly? Did you forget the "454_SETTINGS" in front
of -AS:mrl? And 3 is really really really a bit small.
Thank you for the sugerencia. You have reason, use-AS:mrl=3 has been one
of the multiple tests that I have realized.
For the case explaining to you a bit more, I am ensamblando genomic
sequences and pine contained in vectors BAC, sequenced with 454. One of
the principal characteristics of these sequences is that they possess 70
% of highly repetitive DNA. I have obtained the best results using:
"mira -fasta -project=40B10 -job=denovo,genome,normal,454
-highlyrepetitive -LR:mxti=yes -FN:xtii=40B10_traceinfo_in.454.xml"
If you have really nasty repeats, try "-SK:mnr=yes", but be aware that this
might mask away quite a bunch of data (adjustable via "-SK:rt").
I am going to try to change the parameter that you suggest me.
Thank you very much for everythinng.
Regards,
Rocío Bautista
--
Rocío Bautista Moreno
Centro de Supercomputación y Bioinformática
Universidad de Málaga
EMAIL: rociobm@xxxxxxxxxxx Edificio de Bioinnovación
TELEF: +34952137649 C/ Severo Ochoa 34
FAX : +34952132790 Parque Tecnológico de Andalucía
29590 Málaga (SPAIN)
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