Hello!
I have a question about the NGS: Indel Analysis toolset in
Galaxy. I have aligned my samples from Illumina's HiSeq2000 to the reference
genome using BWA. I've called SNPs using SAMTools and now need to call indels.
Under the NGS: Indel Analysis toolset, I see two
Hello!
I have an RNA-Seq project which consists of 5 samples from the
species tree shrew. When uploading these fastq files into Galaxy, I chose
unspecified (?) for the database/build since the latest tree shrew version is
not in the drop down list. When using TopHat,
and gtf file.
Thanks,
David
-Original Message-
From: Jennifer Jackson [mailto:j...@bx.psu.edu]
Sent: Friday, August 19, 2011 9:20 AM
To: David K Crossman
Cc: galaxy-user (galaxy-user@lists.bx.psu.edu)
Subject: Re: [galaxy-user] Cuffdiff question about using an unspecified (?)
database/build
Jeremy,
The files need to be groomed using the FastQ Groomer so that
they will end up in the fastqsanger state. Then your files will show up in the
pull-down menus.
David
From: galaxy-user-boun...@lists.bx.psu.edu
[mailto:galaxy-user-boun...@lists.bx.psu.edu] On Behalf Of
Hello!
I noticed that Mycoplasma pneumonia M129 and FH are not found
in the reference genome in Galaxy. Would it be possible to have both of those
in there?
Thanks,
David
___
The Galaxy User list should be used for the
it a name (i.e.
gene_name or gene_id) for it to be recognized and if so, how do you assign
column names to GTF files?
Thanks,
David
From: Jeremy Goecks [mailto:jeremy.goe...@emory.edu]
Sent: Thursday, April 07, 2011 9:40 PM
To: David K Crossman
Cc: galaxy-user
Subject: Re: [galaxy-user] RNA
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