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Thread | Thread Starter | Forum | Replies | Last Post |
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#1 |
Registered Vendor
Location: Southern California Join Date: Nov 2007
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Hi all,
Is anyone using Phi29 amplified genomic DNA for next gen? I am specifically interested in using it before 454 for metagenomic analysis but anyone with experience or opinions with other systems would be helpful. The newsbot listed a WGA paper but it wasn't analyzed with a next gen instrument so even though it worked great on a bead array, I'd like to know if it has been validated on sequencing platforms. Thanks, Suzanne
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#2 |
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Location: Korea Join Date: Sep 2008
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In the following paper, the authors used the MDA method (phi29 DNA polymerase) and 454 sequencing for viral metagenomics study.
http://biology.plosjournals.org/perl...l.pbio.0040368 PLoS Biology - The Marine Viromes of Four Oceanic Regions But, MDA may make (maybe significant) quantitative bias on the composition of each member. For MDA bias, you can referr to a paper reporting selective amplification of ssDNA viruses using MDA. http://aem.asm.org/cgi/content/abstract/AEM.01275-08v1 In this paper, circular DNA can be amplified very effectively and alter the composition of the amplified DNA. Last edited by mgenome; 01-22-2009 at 01:30 AM. |
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#3 |
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Location: Southern California Join Date: Nov 2007
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Thanks!!
This is a great help. Suzanne
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#4 |
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Location: Madison Join Date: Mar 2009
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There was another application by the FBI that looked at various ligation conditions prior to WGA.
http://www.promega.com/geneticidproc...ions/Nunez.pdf |
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#5 |
--Site Admin--
Location: SF Bay Area, CA, USA Join Date: Oct 2007
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Here is another paper for answering this question:
Assessment of whole genome amplification-induced bias through high-throughput, massively parallel whole genome sequencing. |
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#6 |
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Location: Southern California Join Date: Nov 2007
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Thanks E- This reference is perfect.
S
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