Details
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Type:
Support
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Status: Closed (View Workflow)
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Priority:
Major
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Resolution: Done
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Labels:None
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Sprint:Sprint 4, Sprint 5
Description
From: "Dingwall, Andrew" <Adingwall@luc.edu>
Date: Mon, 23 Jun 2014 16:47:34 +0000
To: Ann Loraine <aloraine@uncc.edu>
Subject: current genome annotations
Hi Ann,
The IGB version I have been using defaults to the Drosophila melanogaster genome annotation dated 2006. There is a current annotation that is more recent, though I don’t know how to used that one. (The current release of FlyBase (FB2014_03) contains annotation release version 5.57 of D. melanogaster, which will be the last version of the 5.x assembly. Starting with FB2014_04, Flybase is migrating to release 6 of the BDGP assembly).
Is there a simple way to display our ChIP-seq and RNA-seq data on the current genome annotation?
Thanks…
Andrew
Andrew K. Dingwall, PhD
Loyola University Chicago, Health Sciences Division
Stritch School of Medicine
Oncology Research Institute/Gene Regulation and Epigenetics Program
Departments of Pathology and Microbiology & Immunology
2160 S. First Avenue, Cancer Center-334
Maywood, IL 60153
(708) 327-3141; fax (708) 327-3342
Website: http://dingwall-lab.weebly.com/
Attachments
Issue Links
- is duplicated by
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HELP-80
User Support: User requests D. melanogaster (release 6) genome
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- Closed
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From: <Loraine>, Ann <Ann.Loraine@uncc.edu>
Date: Monday, November 24, 2014 at 8:52 AM
To: "Dingwall, Andrew" <Adingwall@luc.edu>
Cc: "Meyer, Mason" <mmeyer20@uncc.edu>, "Freese, Nowlan" <nfreese@uncc.edu>
Subject: Re: IGB update on Drosophila version 6 annotations and genome
Thanks for getting back to me so quickly!
Yes, you probably will need to view the old ChIP-Seq data using the older version. If your older data are BAM, bedgraph or wig files, then they probably reference the older version - dm5. You could probably open your files in the new version, but the alignments will map to the wrong place if the genome has changed a lot - e.g., some parts added or removed.
Probably the best thing would be to re-align your data onto the new version and re-run your old pipeline on it. Depending on when you did your original analysis, you may be pleasantly surprised — much of the software we use for this has improved a LOT in the past few months! You may get better results and the software will like be faster and easier to run.
In my lab, we are using bowtie to align reads and macs2 to find and score peaks. And we’ve started using DiffBind (from Bioconductor) to identify differentially bound peaks across samples.
Also, we'd be happy to help you set up an IGB QuickLoad site you could use to publish/share your data sets. Nowlan Freese and Ivory Blakely (cc’d on this email) can walk you through it, and documentation is here: https://wiki.transvar.org/confluence/display/igbman/Creating+QuickLoad+Sites
Very best wishes,
Ann Loraine