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 optio
t; box for
analyses where I provide the fasta 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
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, Cufflin
Hello!
I have come across a problem where Cufflinks is reporting all
FPKM values as zeroes (0). I have a unique RNA-Seq project from a collaborator
where they are studying eyesight by using tree shrews. I found that Ensembl
(http://useast.ensembl.org/Tupaia_belangeri/Info/Index
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 Je
Hello!
I have 10 human RNA-Seq samples consisting of 3 groups (2
replicates per group). I have already run each of them through TopHat and
Cufflinks on the Penn State Galaxy instance. I am now at a head-scratching
moment. I want to use CuffCompare next (in the end I will want
Hello!
We uploaded 12 samples to Galaxy last night via FTP. This
morning, I went to "Get Data" and clicked on all 12 that were under the FTP
location, chose the type of file they were and reference genome and then
clicked "Excecute." The 12 moved over to the History panel and
Jen,
Thanks for the useful tips! Yes, the NCBI bioproject link is the
correct source for the FH strain.
Thanks,
David
-Original Message-
From: Jennifer Jackson [mailto:j...@bx.psu.edu]
Sent: Tuesday, May 31, 2011 10:07 AM
To: David K Crossman
Cc: galaxy-user
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 dis
ssign 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
Hello!
I would like to ask a question related to this thread below. I
ran into the same issues as below and was unaware of having to swap some
columns around in the GTF file. So, after 'swapping the gene name from the
complete table (name2 value, column 12) into the GFT file
t help me better understand the quality score and which to use?
Any info/help would be greatly appreciated.
Thanks,
David
David K. Crossman, Ph.D.
Systems Biologist/Analyst/Statistician
Heflin Center for Genomic Science
University of Alabama at Birmingham
720 20th Street South
Kaul Room 420
Bir
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