![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
Primer dimer in ChIP-seq library | lavagirl | Sample Prep / Library Generation | 7 | 06-07-2013 05:52 AM |
Rapid Library Library Quantitation using concentration not RFU | GraemeFox | 454 Pyrosequencing | 9 | 10-21-2011 12:27 AM |
NEBNext 454 rapid library | TonyBrooks | Sample Prep / Library Generation | 1 | 08-01-2011 01:56 PM |
Truseq library has dimer/trimer peak on bioanalyzer after amplfication | sehrrot | Sample Prep / Library Generation | 4 | 06-15-2011 04:38 PM |
Inosine in B-adaptor of Rapid Library | Zaag | 454 Pyrosequencing | 7 | 10-20-2010 12:41 PM |
![]() |
|
Thread Tools |
![]() |
#1 |
Junior Member
Location: Perth WA Join Date: Mar 2011
Posts: 1
|
![]()
Hi All,
We have recently done a 454 GS junior run of a rapid library build of some low-copy number aDNA and had an overwhelming number of reads appearing to be dimerisation of our y-adapters. Has anyone else experienced this? Thanks |
![]() |
![]() |
![]() |
#2 |
Junior Member
Location: Germany Join Date: Oct 2010
Posts: 1
|
![]()
What i did was made aDNA library using RAPID lib Kit. Amplified with emPCR primer and then cloned the amplified library to ensure fragment-adaptor ligation. of course my purpose was to enrich using NimbleGen array prior to 454 GS junior sequencing!!
|
![]() |
![]() |
![]() |
Tags |
454, low copy, rapid library |
Thread Tools | |
|
|