Then, you should read this first. http://sourceforge.net/apps/mediawiki/wgs-assembler/index.php?title=PacBioToCA PacBio reads must be corrected using reads from other technologies, or self-corrected, before being able to do anything. Cheers, Juan On Wed, Feb 19, 2014 at 6:23 PM, DUBOST AUDREY <Audrey.Dubost@xxxxxxxxxxxxx>wrote: > Just the filtered raw reads > > Audrey > > > > *De :* mira_talk-bounce@xxxxxxxxxxxxx [mailto: > mira_talk-bounce@xxxxxxxxxxxxx] *De la part de* Andrej Benjak > *Envoyé :* mercredi 19 février 2014 10:22 > *À :* mira_talk@xxxxxxxxxxxxx > *Objet :* [mira_talk] Re: pacbio reads on debrislist > > > > I am curious, are the PacBio reads error corrected or just the filtered > raw reads? > > Andrej > > On 02/19/2014 10:01 AM, DUBOST AUDREY wrote: > > Hello, > > I have a question with MIRA4. > > I want to assemble pacbio reads and illumina reads. > > > > First, I want to test only pacbio reads, all parameters are in manifest > file like this: > > project = variant180214 > > job = genome,denovo,accurate > > parameters =-NW:mrnl=0 -SK:mmhr=1 -NW:cac=no -GE:not=10 -AS:nop=1 > -HS:ldn=y -CO:mr=no\ > > PCBIOHQ_SETTINGS -AS:mrpc=1 -OUT:sssip=y > > # defining the paired-end Illumina reads, fixing all needed pair > information > > # defining the pacbio reads, fixing all needed pair information > > readgroup = Pacbio > > data = variant_in.pacbio.fastq > > technology = pcbiohq > > > > To accelerate computation time I have taken -AS:nop to 1 , AS:mrpc=1 > (because I want to put illumina reads after this assembly) > > On 200 000 pacbio reads, only 2500 are used in assembly...the rest is on > debrislist with "no_overlap" so I try with -HS:ldn=y -CO:mr=no but it > change nothing... > > > > Do you have any idea of this problem? > > Thanks in advance > > > > > -- Juan Pascual-Anaya, PhD Research Scientist Laboratory for Evolutionary Morphology Center for Developmental Biology (CDB) RIKEN 2-2-3 Minatojima-minamimachi Chuo-ku, Kobe, Hyogo 650-0047 Japan