Indeed, I have rewritten the code with the Peter suggestions and I was thinking to update the PR with this code On 6 May 2015 at 17:45, Joshua Udall <jaudall1@gmail.com> wrote:
Use subBam from the BamBam package. Written in C.
subBam -g targets.bed sorted.bam -o sorted.subset.bam -m 0
http://sourceforge.net/projects/bambam/
On Wed, May 6, 2015 at 4:23 AM, Peter Cock <p.j.a.cock@googlemail.com> wrote:
Hi Roberto,
Given the way BAM indexing works, I see no reason to actually split the BAM file at all - it seems like wasted disk IO.
Instead, can you split a BED file into sub-regions? This way each child GATK job would look at the full BAM file but only for a small region described in the split BED region file?
Peter
Hello,
I have been working in the Galaxy parallelization module and I would
ask you some questions that I have about how to face one problem. I have done one pull request about splitting bams: https://github.com/galaxyproject/galaxy/pull/184
Regarding this, I think it is useful but it could be more while accessing somehow the interval. I better explain it with an example: If I define a simple tool like this, with the parallelism tag "actived":
<tool id="gatk" name="call with gatk"> <description>gatk</description> <parallelism method="multi" split_mode="by_interval" split_size="100000000" merge_outputs="output" split_inputs="input"
</parallelism>
<command> ## by_rname ln -s $input input.bam; samtools index input.bam; UnifiedGenotyper -R /home/ralonso/BiB/Galaxy/data/hg19_ucsc.fa -I input.bam -o $output -L REGION ;
</command> <inputs> <param format="bam" name="input" type="data" label="bam"/> </inputs> <outputs> <data format="vcf" name="output" /> </outputs>
<help> bwa </help> </tool>
The region is based on the field split_size, it is better explained in
PR. How does the code from the PR work? It goes through the bam file and does something like "samtools view REGION -o bam_splitted.bam", so then GATK does the calling for this small bam, but what is the problem? As you know, in the software GATK if you don't pass the region as an argument in the command line it goes through all the genome, so it is very slow. So, what would you recommend to me to be able to pass this information to GATK? I was
On Wed, May 6, 2015 at 11:19 AM, Roberto Alonso CIPF <ralonso@cipf.es> wrote: like to the thinking
to create, at the same time the bam is splitted, a file region.bed and use it in the tool definition xml, so the command would be like this: <command> ... UnifiedGenotyper -R /home/ralonso/BiB/Galaxy/data/hg19_ucsc.fa -I input.bam -o $output -L region.bed; </command>
This solution does not convince me too much because it is a bit intrusive in the tool definition and also because you have to trust that the region.bed file exists. Do you have any opinion, suggestion...?
Thanks a lot!
Best regards
-- Roberto Alonso Functional Genomics Unit Bioinformatics and Genomics Department Prince Felipe Research Center (CIPF) C./Eduardo Primo Yúfera (Científic), nº 3 (junto Oceanografico) 46012 Valencia, Spain Tel: +34 963289680 Ext. 1021 Fax: +34 963289574 E-Mail: ralonso@cipf.es
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-- Joshua Udall (5133 LSB) Brigham Young University 701 E. University Parkway Plant and Wildlife Science Depart. Provo, UT 84602
Office: 801-422-9307
-- Roberto Alonso Functional Genomics Unit Bioinformatics and Genomics Department Prince Felipe Research Center (CIPF) C./Eduardo Primo Yúfera (Científic), nº 3 (junto Oceanografico) 46012 Valencia, Spain Tel: +34 963289680 Ext. 1021 Fax: +34 963289574 E-Mail: ralonso@cipf.es