Forum: Illumina/Solexa
10-27-2011, 10:54 AM
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Replies: 16
Views: 3,454
I feel the same. at first look ,they look like...
I feel the same. at first look ,they look like PCR duplicates and hence overamplification of the samples. I would contact the person making the libraries and get details on amount of input DNA. If...
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Forum: Ion Torrent
10-22-2011, 08:39 PM
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Replies: 15
Views: 7,349
Seq analysis time difference
Thanks for the informative article. I was wondering what is difference in processing time for sequence analysis for the 314, 316 and 318 chips.
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Forum: Illumina/Solexa
09-08-2011, 01:17 PM
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Replies: 7
Views: 2,200
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Forum: Illumina/Solexa
09-08-2011, 11:08 AM
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Replies: 7
Views: 2,200
Aplany, I am trying to answer your question in...
Aplany, I am trying to answer your question in three parts. third part is main explaination.
You can mix pool libraries at different concentration. Theoreticall you will get the reads in the same...
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Forum: Sample Prep / Library Generation
07-06-2011, 11:45 PM
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Replies: 3
Views: 4,891
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Forum: Sample Prep / Library Generation
06-30-2011, 10:59 AM
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Replies: 0
Views: 2,184
Library efficiency using Agilent Surelect
I am interested in knowing the efficiency of different library prep methods.
I want to to compare the blunt end ligation with a-tail and especially comparing the different kits available in the...
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Forum: Events / Conferences
10-11-2010, 01:54 PM
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Replies: 15
Views: 8,974
Presentation Link
In case you missed the meeting or are interested in the presentations of the meeting, please shoot me an email and I will send the username and password
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Forum: Events / Conferences
09-07-2010, 03:28 PM
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Replies: 15
Views: 8,974
I am interested in going for the evolution of...
I am interested in going for the evolution of next generation sequencing conference. Working in the area, it's time to learn about more applications for next generation sequencing and this seems a...
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