![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
Very Large Mate Pair Libraries | Daytwa | Illumina/Solexa | 7 | 04-21-2015 02:37 AM |
Mate pair libraries with longer read length | rakesh.ponnala | Illumina/Solexa | 4 | 01-16-2012 03:41 PM |
exome enriched mate-pair libraries | upenn_ngs | Illumina/Solexa | 0 | 07-29-2011 10:26 AM |
Use of illumina mate pair libraries for scaffolding | glacerda | Bioinformatics | 2 | 07-13-2011 08:35 AM |
Illumina mate-pair analysis | shu | Bioinformatics | 0 | 02-10-2010 05:07 AM |
![]() |
|
Thread Tools |
![]() |
#1 |
Registered Vendor
Location: Socal Join Date: Apr 2008
Posts: 6
|
![]()
Anyone sequencing mate pair libraries beyond the recommended 36bp?
Thanks, Phillip |
![]() |
![]() |
![]() |
#2 |
Junior Member
Location: Belgiium Join Date: Mar 2010
Posts: 2
|
![]() |
![]() |
![]() |
![]() |
#3 |
Junior Member
Location: Flagstaff Join Date: Apr 2010
Posts: 1
|
![]()
I recently did a 101-bp run with indexed mate pairs. Rather than cut out a 300-400 bp chunk at the second fragmentation step, I took a 600 bp chunk. So far, we have not seen any odd bioinformatic results indicating a junction-point issue. That said, you can always just trim the ends if it is of concern. I indexed the mate pair and had it in with 4 other bugs that I prepared as paired end. The mate-pair sample definitely was the cleanest of the group, i.e. better quality scores toward the end of the reads.
|
![]() |
![]() |
![]() |
Thread Tools | |
|
|