I am playing with Galaxy "splitters" capabilities. After some cases that
you help me out to solve I am facing a new issue, this is maybe due to my
tool configuration file, but in any case I tell you what I've done.
What I would like to do exactly, is to split paired fastq, map them and
then join them. This is my configuration file:
<tool id="bwa_mio" name="map with bwa">
<description>map with bwa</description>
<parallelism method="basic" split_size="3" split_mode="number_of_parts"
bwa mem -R '@RG\tID:foo\tSM:bar'
/home/ralonso/BiB/Galaxy/data/Cclementina_v1.0_scaffolds.fa $input >
temporary_bam_file.sam 2>/dev/null ;
samtools view -Sb temporary_bam_file.sam > temporary_bam_file.bam ;
samtools sort temporary_bam_file.bam $output ;
<param format="fastqsanger" name="input" type="data" label="fastq"/>
<data format="bam" name="output" />
My problem of this configuration is that generates an empty file. So, after
seeing the code, I discover that when it tries to join the several bam
files it goes to the first parent: *class Data( object )*, to the method
merge: *def merge( split_files, output_file). *So I may be wrong, but I
think binary.bam class should override this method, is this right? if this
is the case, I would like to implement this method, I have couple of basic
ideas, like merge them with samtools. What do you think?
On ther other hand, is this related with the last email of John Chilton and
the 15.03 release?
Functional Genomics Unit
Bioinformatics and Genomics Department
Prince Felipe Research Center (CIPF)
C./Eduardo Primo Yúfera (Científic), nº 3
46012 Valencia, Spain
Tel: +34 963289680 Ext. 1021
Fax: +34 963289574
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