Hi, I'm trying to solve an issue I'm having with my local installation of
Galaxy (installed on my own computer, rather than on a server). I'm using
data in the form of fastq files from an Illumina Hi-seq and I want Galaxy
to parse the bar coded sequences out into individual files for me. I've
been
Hi Judith,
The analysis in the paper focused on profiling taxonomic ranks. This was
done with Megablast versus the GenBank databases NT & WGS. The accession
identifiers being associated with nucleotide data, not protein (as would
result from a comparison against NR), is most likely the problem
Yes that was it! I knew I was missing something obvious.
Thanks,
Greg
On Wed, Oct 10, 2012 at 9:06 AM, Dannon Baker wrote:
> Looking at your screenshot, you have "Use a built-in index" selected. If you
> change this to "Use one from the history", do you see your fasta file listed?
>
> -Danno
Looking at your screenshot, you have "Use a built-in index" selected. If you
change this to "Use one from the history", do you see your fasta file listed?
-Dannon
On Oct 10, 2012, at 9:02 AM, greg wrote:
> Thanks Jen. But it looks like the datatype was already set to fasta.
> I tried setting
Thanks Jen. But it looks like the datatype was already set to fasta.
I tried setting it again and saving but it didn't seem to help.
Is there anything else I can try?
thanks,
Greg
On Tue, Oct 9, 2012 at 9:10 PM, Jennifer Jackson wrote:
> Hi Greg,
>
> Nice pic, it helps! My guess is that the d
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