Edit: Updated few Links.
Hello,
I'm trying to self-correct PacBio long fastq sequences using Celera 8.2 assembler through the PBcR pipeline.
Since the pacbio.spec option is mandatory, can anybody explain me how a correct minimal pacbio.spec file should be built?
Thank you in advance for your help!
1 answer
The pacbio.spec file is for Celera Assemler. Here are the two example files:
Multicore machine: http://www.cbcb.umd.edu/software/PBcR/data/selfSampleData/pacbio.spec
SGE version: http://www.cbcb.umd.edu/software/PBcR/data/sampleData/pacbio.SGE.spec
The options are well documented here.
From the tutorial do you have any idea about the -l parameter;
% <wgs>/<Linux-amd64>/bin/PBcR -length 500 -partitions 200 -l lambdaIll -s pacbio.spec -fastq pacbio.filtered_subreads.fastq genomeSize=50000 illumina.frg
I think it just give a name to result but for example when I want to direct the output to different directory it does not work;
% <wgs>/<Linux-amd64>/bin/PBcR -length 500 -partitions 200 -l /home/user/test/lambdaIll -s pacbio.spec -fastq pacbio.filtered_subreads.fastq genomeSize=50000 illumina.frg
Any idea?
I tried PBcR --help but there is no info about it is there any will documented information about the software?
Thats the library name. Not the Path.
So how can I direct the output to the path I want?
I do not see any option for that. http://wgs-assembler.sourceforge.net/wiki/index.php/PBcR
Whats the error when you give path to -l?
It will not work and give you the message can not create temp/"the path you want"
Generally I found a work around that just run the command from the place you want your output to be, but I do not think that it is logical or even good idea that is why I asked :D
Log in to answer this question.