Re: [galaxy-user] Cuffdiff changes

2013-08-23 Thread Jeremy Goecks
 Where can I see which version are being used?

You can see both the Galaxy tool version and the Cuffdiff tool version (when 
available) by clicking on the 'view details' icon (the 'i' at the bottom of an 
expanded dataset). Right now the Cuffdiff version is not displayed, but that 
will change when our server is updated.

 What does Cuffdiff(version 0.0.5) mean then?

That is the version of the Galaxy wrapper; the wrapper provides the interface 
between Cuffdiff and Galaxy.

 What version was it before?

I think Cuffdiff version was 1.3.1 previously.
 
 I look forward to the update, will that mean another version of Cuffdiff 
 again?

The wrapper will be updated but not Cuffdiff itself.

J.

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Re: [galaxy-user] Cuffdiff changes

2013-08-23 Thread Johanna Sandgren
Thanks for quick reply.

Where can I see which version are being used? It does not say in the attached 
(in my first e-mail) info-view  after the run.. What does Cuffdiff (version 
0.0.5) mean then? What version was it before? It is a great difference in 
number of DE genes..

I mostly meant it was the same now in August with more DE genes for all 
different type of analysis that I have previously done (consistent new results 
with no settings changed), I really do not see more DE genes when 5 vs 6 
samples compared to 1 vs 2 samples. But that might be due to more biological 
reasons.

I look forward to the update, will that mean another version of Cuffdiff again?

Kind regards,
Johanna

From: Jeremy Goecks [mailto:jeremy.goe...@emory.edu]
Sent: Thursday, August 22, 2013 8:04 PM
To: Johanna Sandgren
Cc: galaxy-user@lists.bx.psu.edu
Subject: Re: [galaxy-user] Cuffdiff changes

I am wondering why Cuffdiff suddenly gives many more significant DE genes?

Cuffdiff was recently updated to version 2.1.0; this update likely explains the 
different results that you see.


I have rerun several analysis, also with more samples in each group, all give 
much more significant genes. Why?

More samples = more power to accurately estimate expression levels = more DE 
genes.


Also, will replicate information soon be included in output files?

Replicate data will be available when we next update our server. This should 
occur in about 3 weeks.

Best,
J.

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[galaxy-user] Cuffdiff changes

2013-08-22 Thread Johanna Sandgren
Hi,

I am wondering why Cuffdiff suddenly gives many more significant DE genes?
I have used same input data and now get approx 5x more significant genes, 
settings is same with the exception that you now included library normalization 
and dispersion estimation. See below for parameters.
I have rerun several analysis, also with more samples in each group, all give 
much more significant genes. Why?

Also, will replicate information soon be included in output files?

Kind regards,
Johanna


Tool: Cuffdiff

Tool: Cuffdiff

Name:

Cuffdiff on data 225, data 236, and others: splicing differential expression 
testing

Name:

Cuffdiff on data 225, data 236, and others: splicing differential expression 
testing

Created:

4-Apr-13

Created:

21-Aug-13

Filesize:

10.3 MB

Filesize:

10.2 MB

Dbkey:

hg19

Dbkey:

hg19

Format:

tabular

Format:

tabular

Galaxy Tool Version:

0.0.5

Galaxy Tool Version:

0.0.5

Tool Version:

Tool Version:

Tool Standard Output:

stdouthttps://main.g2.bx.psu.edu/datasets/bbd44e69cb8906b5355e4a035e92cd84/stdout

Tool Standard Output:

stdouthttps://main.g2.bx.psu.edu/datasets/bbd44e69cb8906b524bcf7e585f495b1/stdout

Tool Standard Error:

stderrhttps://main.g2.bx.psu.edu/datasets/bbd44e69cb8906b5355e4a035e92cd84/stderr

Tool Standard Error:

stderrhttps://main.g2.bx.psu.edu/datasets/bbd44e69cb8906b524bcf7e585f495b1/stderr

Tool Exit Code:

0

Tool Exit Code:

0

API ID:

bbd44e69cb8906b5355e4a035e92cd84

API ID:

bbd44e69cb8906b524bcf7e585f495b1


Input Parameter

Value

Note for rerun

Input Parameter

Value

Transcripts

261: Cuffmerge on data 258, data 135, and others: merged transcripts

Transcripts

261: Cuffmerge on data 258, data 135, and others: merged transcripts

Perform replicate analysis

Yes

Perform replicate analysis

Yes

Group name

s202

Group name

s202

Add file

194: Galaxy883-[MarkDups_Dupes_Marked_882_202.bam].bam

Add file

194: Galaxy883-[MarkDups_Dupes_Marked_882_202.bam].bam

Group name

Ctrls

Group name

Ctrls

Add file

236: MarkDups_Dupes Marked216.bam

Add file

236: MarkDups_Dupes Marked216.bam

Add file

225: MarkDups_Dupes Marked206.bam

Add file

225: MarkDups_Dupes Marked206.bam

Library normalization method

not used (parameter was added after this job was run)

Library normalization method

geometric

Dispersion estimation method

not used (parameter was added after this job was run)

Dispersion estimation method

pooled

False Discovery Rate

0.05

False Discovery Rate

0.05

Min Alignment Count

2

Min Alignment Count

2

Perform quartile normalization

No

Perform quartile normalization

No

Use multi-read correct

Yes

Use multi-read correct

Yes

Perform Bias Correction

Yes

Perform Bias Correction

Yes

Reference sequence data

cached

Reference sequence data

cached

Set Additional Parameters? (not recommended)

Yes

Set Additional Parameters? (not recommended)

Yes

Average Fragment Length

200

Average Fragment Length

200

Fragment Length Standard Deviation

80

Fragment Length Standard Deviation

80



..
Johanna Sandgren, PhD
Department of Oncology-Pathology
CCK, Karolinska Institutet
SE-171 76 Stockholm, Sweden
+46-8-517 721 35 (office),
+46-8- 321047(fax), +46-708 388476 (mobile)

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