Dear All,I am trying to run mira for ion proton plant transcriptome data(2 GB) mean read length is between (90-130) for all the 6 sample together. It comes under solanum genus. In the assembly only 20% reads are used.
Is it likly possible because low data or I am lacking in parameters?Please find below parameter which I have used. For Ion data is it trim the low quality bases (phred<20) By default it trims (phred<15) I have used default?
project = sample1 job = est, denovo, accurate parameters = COMMON_SETTINGS -GE:not=30 \ --noclipping \ IONTOR_SETTINGS -AS:mrpc=50 readgroup = ion_single technology = iontor data = sample1.fastqI have another question regarding Whole genome denovo assembly for bacteria. It is a 5 MB Genome. I have obtained 80X coverage (Ion proton) data (mean read length 150). But after assembly (I am getting >2000 contigs). For this also I have used same above parameter except est option. I have two doubts,
What could be the reason for more number of contigs(may be repeat, GC, Genome complexity) but how to find out which is the one?
or Is there any problem in the parameter? Looking forward for your help, Regards, Manoharan -- 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