Respected Sir / Ma'am,
'x' tool having 3 commands,
1) command takes files from path. ex
perl x.pl --mode 1 file1.bam file2.bam file3.fasta --output result1.txt
2) file4 must have name of result1.txt, file1.bam, file2.bam
perl x.pl --mode 2 file4.txt --output-directory ~/result2/
for this
Hello!
I use Galaxy to convert unaligned .bam files (RNA-seq) to fastq files.
That works! Then i want to align the fastq files using TopHat2 or
Tophat, but the analysis does not start since yesterday. However, I
received the following error message several times since yesterday:
Details
Hi David,
I think that you are asking about the locally cached reference genome
builds - also sometimes called 'built-in'? If so, these wikis have
instructions to help you create, organize, and obtain these data (if you
want copies of what we host on Main).
Reference genome builds can seem
Hi Chetan,
try to use the configfile feature to create file4.txt ...
https://wiki.galaxyproject.org/Admin/Tools/ToolConfigSyntax#A.3Cconfigfiles.3E_tag_set
Cheers,
Bjoern
Am 04.03.2014 15:04, schrieb do kadya:
Respected Sir / Ma'am,
'x' tool having 3 commands,
1) command takes files from
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