I'm trying to create a RNA-Seq Workflow with Bowtie/Tophat and Cufflinks using a newly
assembled genome (not public). I created the genome index files via Bowtie locally but
Galaxy will not accept the .ebwt index files (n=4)--"Inappropriate content"
Galaxy will not accept Bowtie indices. When you provide Bowtie/Tophat with a
custom genome via Galaxy, Galaxy will create the indices needed for the tool to
run before running the tool.
Second, for some reason, the Illumina fastq files will not load on the web
version or my local version either.
You'll need to groom the files to convert them from fastq format to fastqsanger
format, which is the format accepted by Galaxy's NGS tools. See the
FastqGroomer tool for details. (If you're confident your fastq quality scores
are in Sanger format, you can simply change the fastq dataset's datatype by
clicking on its pencil and looking for the datatype selection on the page. This
will take less time than running the groomer.)
Assuming you are confident of the fastq format, is there anyway to do this
non-interactively, so you can run bowtie directly on the fastq sequences
without using FastqGroomer (for example, in a Workflow)?
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