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Thread | Thread Starter | Forum | Replies | Last Post |
poor amplification with fusion primers | Seqasaurus | 454 Pyrosequencing | 3 | 05-23-2013 07:20 AM |
Illumina PE primers | Zebrafish | Sample Prep / Library Generation | 0 | 05-11-2012 09:29 AM |
Illumina Pair end primers and adaptors for multiplexing | mimi_lupton | Sample Prep / Library Generation | 1 | 05-25-2011 08:57 AM |
HPLC purification of 454 fusion primers | skolyar | 454 Pyrosequencing | 2 | 09-22-2010 01:40 PM |
Illumina Primers | Will | Illumina/Solexa | 1 | 08-10-2009 09:08 AM |
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#1 |
Junior Member
Location: Colorado Join Date: Jul 2012
Posts: 1
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Anyone preparing ITS amplicon libraries for use on a MiSeq platform? Care to share any of your primer designs? Need to start examining fungal communities and trying not to reinvent the wheel.
Thanks! |
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#2 |
Junior Member
Location: Davis, CA Join Date: Apr 2013
Posts: 2
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I'm wondering the same thing. What did you end up doing? Any suggestions?
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#3 |
Junior Member
Location: Switzerland Join Date: Jan 2013
Posts: 2
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Hi There,
I have the protocol for ITS Fungal in HiSeq working. New forward primer, better coverage than the previous described, we are preparing the paper now. Cheers Eric |
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#4 |
Junior Member
Location: Ottawa ON Canada Join Date: Jun 2013
Posts: 2
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I am currently designing Illumina fusion primers but am getting a bit worried. I don't want to get stuck buying 96 unique really long fusion primers (I want dual indexing). Do you know of anyone using complete fusion primers (adaptor+seq primer+index+PCR primer) VERSUS ligating adaptor+seq primer+index to standard PCR product after amplification?
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#5 |
Junior Member
Location: USA Join Date: Dec 2013
Posts: 1
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Hi Eric, would like to check if your paper already published. If so, could you please send me the link and share the protocol &primers? Thank you so much!!
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