Re: [galaxy-user] Tophat alignment statistics?

2012-12-06 Thread Praveen Raj Somarajan

Hi Wei,

Have a look at RNASeQC which provides more than what you specified here. 
(https://confluence.broadinstitute.org/display/CGATools/RNA-SeQC)
This generates a detailed report with all relevant metrics on your RNA data.. I 
think, integrating this - a java based tool - into Galaxy should resolve your 
problem.

Hope this helps.

Raj

From: galaxy-user-boun...@lists.bx.psu.edu 
[mailto:galaxy-user-boun...@lists.bx.psu.edu] On Behalf Of Wei Liao
Sent: Friday, December 07, 2012 3:57 AM
To: galaxy-user@lists.bx.psu.edu
Subject: [galaxy-user] Tophat alignment statistics?

Hi, galaxy users

How to get Tophat alignment statistics such as % of reads aligned to exon, 
intron, splice junction? is there a Log file available?
How many unique and mutiple alignments?
I use Bam index, Flagstat, and Bam alignment metrix in Galaxy, but none 
reported the information I need.

--
Wei Liao
Research Scientist,
Brentwood Biomedical Research Institute
16111 Plummer St.
Bldg 7, Rm D-122
North Hills, CA 91343
818-891-7711 ext 7645



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[galaxy-user] Why doesn't bowtie in galaxy accepting colorspace reads directly?

2012-09-15 Thread Praveen Raj Somarajan

Hi All,

I'm wondering why the Bowtie version in (even latest) Galaxy does NOT support 
.csfasta/.qual input files directly, though it is mentioned under "Map with 
Bowtie for SOLiD". This is the case of "BWA for SOLiD" as well. One would 
expect direct support on colorspace files. Do you have any plans of 
implementing this?I see this would be a great support to SOLiD users.

Look forward to your comments

Thanks,
Raj






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[galaxy-user] Indexing files everytime - Performance Issue

2012-07-03 Thread Praveen Raj Somarajan

All,

It is noticed that Galaxy/GATK indexes reference fasta & dbSNP file everytime 
when it runs. Re-indexing takes time (~10min), hence it affects overall run 
time when it use for multiple times. However, this could be avoided by reusing 
the available index. Here is the snapshot of the log:

INFO  11:43:57,365 HelpFormatter - The Genome Analysis Toolkit (GATK) 
v1.4-21-g30b937d, Compiled 2012/02/01 19:01:14
INFO  11:43:57,365 HelpFormatter - Copyright (c) 2010 The Broad Institute
INFO  11:43:57,365 HelpFormatter - Please view our documentation at 
http://www.broadinstitute.org/gsa/wiki
INFO  11:43:57,366 HelpFormatter - For support, please view our support site at 
http://getsatisfaction.com/gsa
INFO  11:43:57,367 HelpFormatter - 
-
INFO  11:43:57,429 GenomeAnalysisEngine - Strictness is STRICT
INFO  11:43:57,432 ReferenceDataSource - Index file 
/tmp/tmp-gatk-6jlUfH/gatk_input.fasta.fai does not exist. Trying to create it 
now.
PROGRESS UPDATE: file is 15 percent complete
PROGRESS UPDATE: file is 28 percent complete
PROGRESS UPDATE: file is 91 percent complete
INFO  11:45:32,231 ReferenceDataSource - Dict file 
/tmp/tmp-gatk-6jlUfH/gatk_input.dict does not exist. Trying to create it now.
INFO  11:45:54,262 SAMDataSource$SAMReaders - Initializing SAMRecords in serial
INFO  11:45:54,280 SAMDataSource$SAMReaders - Done initializing BAM readers: 
total time 0.02
INFO  11:45:54,304 RMDTrackBuilder - Creating Tribble index in memory for file 
/tmp/tmp-gatk-6jlUfH/input_dbsnp_0.vcf
INFO  11:48:05,910 RMDTrackBuilder - Writing Tribble index to disk for file 
/tmp/tmp-gatk-6jlUfH/input_dbsnp_0.vcf.idx

Do we have any option/alternate in Galaxy to avoid this re-indexing at /tmp, as 
I have already built the index for reference and dbSNP.

Look forward to any suggestions.

Thanks,
Raj



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[galaxy-user] Multiple sample runs using workflow

2012-04-04 Thread Praveen Raj Somarajan

Hello All,

I'm seeking help on how do we run a workflow (say bwa mapping on PE data) on 
multiple samples (eg: 10 samples, PE data) together. I assume "multiple input 
files selection" option does not work here as the workflow accepts two fastq 
input files (PE data). Do you have any experience on this?

Best,

Raj


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Re: [galaxy-user] Error in DepthOfCoverage (GATK) tool

2012-03-01 Thread Praveen Raj Somarajan

Hello Dan,


But, I am currently using the latest update of Galaxy (as 'hg incoming' says 
'no changes'). Just to clarify one thing: which repository should I clone - 
https://bitbucket.org/galaxy/galaxy-dist/ (mentioned in GetGalaxy.org) OR 
http://www.bx.psu.edu/hg/galaxy/ (mentioned in NewsBrief website). I use the 
first one to update Galaxy. I tried to pull the below changeset, but it says 
'invalid revision'.


Please suggest.

Best,

Raj


From: Daniel Blankenberg [mailto:d...@bx.psu.edu]
Sent: Thursday, March 01, 2012 8:45 PM
To: Praveen Raj Somarajan
Cc: galaxy-user@lists.bx.psu.edu
Subject: Re: [galaxy-user] Error in DepthOfCoverage (GATK) tool

Hi Raj,

Thanks for reporting, this issue has been resolved in changeset 
6778:35be930b21be.  Please let us know if you encounter further issues.


Thanks for using Galaxy,

Dan


On Mar 1, 2012, at 3:30 AM, Praveen Raj Somarajan wrote:


Hello,

I'm facing an issue with "Depth Of Coverage" tool when it runs on refGene and 
target BED file. The error message is:

File "cheetah_DynamicallyCompiledCheetahTemplate_1330588825_26_16118.py", line 
402, in respond
NotFound: cannot find 'omit_interval_statistics' while searching for 
'gatk_param_type.omit_interval_statistics'

I noticed that the issue is only when the "Advanced GATK options" is enabled to 
set target BED file.

The commandline runs perfectly with the input files, but galaxy fails due to 
this error. Can anyone suggest what's the issue?

Best,

Raj


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[galaxy-user] Error in DepthOfCoverage (GATK) tool

2012-03-01 Thread Praveen Raj Somarajan

Hello,

I'm facing an issue with "Depth Of Coverage" tool when it runs on refGene and 
target BED file. The error message is:

File "cheetah_DynamicallyCompiledCheetahTemplate_1330588825_26_16118.py", line 
402, in respond
NotFound: cannot find 'omit_interval_statistics' while searching for 
'gatk_param_type.omit_interval_statistics'

I noticed that the issue is only when the "Advanced GATK options" is enabled to 
set target BED file.

The commandline runs perfectly with the input files, but galaxy fails due to 
this error. Can anyone suggest what's the issue?

Best,

Raj


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[galaxy-user] snpEff: html report is not displaying after update

2012-02-15 Thread Praveen Raj Somarajan

Hi All,

I updated galaxy recently to the latest version. Everything looks fine, except 
snpEff report html view. It was displaying properly (all tables and summary 
values) before the update, but the summary values are not displaying after the 
update. A sample screen-shot is attached for your reference. Could you please 
figure out this issue?

When I ran the same on command line, the reports were generated correctly. I 
assume, something (datatypes or preview) has changed by the update. Please let 
me know the work around on this?

Secondly, as we know, snpEff also generates a gene-wise annotation file along 
with other results, but somehow we cannot access this file through Galaxy. 
Though we see the link in the html report, but it seems the path is broken.

Let me know your suggestions.

Best,

Raj



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Re: [galaxy-user] Genomic interval file for GATK

2011-12-12 Thread Praveen Raj Somarajan

Thanks Carlos. For Q#1, I found something that GATK v1.3 does not explicity 
check the format of -L input file, hence the error. And the work around for 
commandline is to specify the format with -L, as shown below:

-L:bed 

Any idea how to edit the wrapper code to resolve this issue in Galaxy? Has 
anybody experienced/resolved this before?

Thanks,

Raj.

From: Carlos Borroto [mailto:carlos.borr...@gmail.com]
Sent: Thursday, December 08, 2011 7:43 PM
To: Praveen Raj Somarajan
Cc: galaxy-user@lists.bx.psu.edu
Subject: Re: [galaxy-user] Genomic interval file for GATK

Hi Raj,

I've been also testing GATK Beta pipeline on Galaxy. This is the workflow I 
have so far:
http://test.g2.bx.psu.edu/u/cjav/w/gatk

There are a few error coming up that I haven't had the time to fix or work 
around yet, but I think it could be a good starting point. For example an issue 
with annotations in Variant Recalibrator tool, was recently fixed:
https://bitbucket.org/galaxy/galaxy-central/issue/682/variant-recalibrator-error-with

I haven't yet used the new manual method to enter annotations in the workflow.

Regarding your questions, I don't have one for 1), I would love to hear about a 
solution. In my case I'm working with RNA-seq data, so I think everything would 
speed up if I use a good interval file, but is not clear for me at the moment 
how to use it or when.

For 2), every time a tool outputs a BAM file in Galaxy, it is sorted and 
indexed automatically, in fact even if the downstream tool can use a SAM file, 
I still convert it to BAM just to make sure it is sorted and indexed.

Regards,
Carlos

On Thu, Dec 8, 2011 at 1:11 AM, Praveen Raj Somarajan 
mailto:pravee...@ocimumbio.com>> wrote:
All,

I'm using a locally installed galaxy with GATK 1.3 beta (recently updated). I 
would be interested in variant calling using GATK on both Illumina and SOLiD 
data. My questions are:

1) What should be the format that "Genomic Interval" option can accept in beta 
version. It produced an error when I provided an (enrichment coords) bed file? 
DepthOfCoverage had also produced error when I used bed files. Would beta 
release (v1.3) accept bed file as input for genomic intervals?

2) SAMtool index is seem to be missing in Galaxy. Is this true or any other 
module (say SAM->BAM) incorporates this functionality?

Looking forward to your comments.

Raj




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[galaxy-user] Genomic interval file for GATK

2011-12-07 Thread Praveen Raj Somarajan

All,

I'm using a locally installed galaxy with GATK 1.3 beta (recently updated). I 
would be interested in variant calling using GATK on both Illumina and SOLiD 
data. My questions are:

1) What should be the format that "Genomic Interval" option can accept in beta 
version. It produced an error when I provided an (enrichment coords) bed file? 
DepthOfCoverage had also produced error when I used bed files. Would beta 
release (v1.3) accept bed file as input for genomic intervals?

2) SAMtool index is seem to be missing in Galaxy. Is this true or any other 
module (say SAM->BAM) incorporates this functionality?

Looking forward to your comments.

Raj




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[galaxy-user] FASTQ Groomer before BWA mapping ?

2011-12-07 Thread Praveen Raj Somarajan

All,

I'm wondering why do we need to convert Illumina FASTQ into sanger using FastQ 
Groomer before mapping with BWA in galaxy. The lastest version of BWA itself 
added -I option to use Illumina data directly. What's your opinion on this?

Secondly, I found that "Map with BWA for Illumina" uses -I option in the 
commandline during execution, even for sanger formatted reads. How does it 
impact the results?

Thanks,

Raj


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