![]() |
|
|||||||
Similar Threads
|
||||
| Thread | Thread Starter | Forum | Replies | Last Post |
| Calling variants in a group of samples sharing a haplotype? | Alex Coventry | Bioinformatics | 0 | 08-16-2011 11:39 AM |
| How to separate individual sample variants from multiple samples | meher | Bioinformatics | 0 | 06-30-2011 12:11 PM |
| Multiplex more than 12 samples? | cybeline | Illumina/Solexa | 4 | 01-25-2011 05:33 AM |
| PubMed: Deep sequencing to reveal new variants in pooled DNA samples. | Newsbot! | Literature Watch | 0 | 10-21-2009 02:02 AM |
| Error-correcting barcoded primers for pyrosequencing hundreds of samples in multiplex | ECO | Literature Watch | 0 | 02-12-2008 10:30 PM |
![]() |
|
|
Thread Tools |
|
|
#1 |
|
Member
Location: Malmö Join Date: Sep 2008
Posts: 37
|
Dear all,
I would like to know if someone is working (or knows someone that is working) on a method to be able to multiplex sequencing of very few variants (let say 100 SNPs) on hundreds or maybe thousands of samples in a single HiSeq run. There is a market need for this kind of product but as far as I know, no solutions are yet available. |
|
|
|
|
|
#2 |
|
Senior Member
Location: St. Louis Join Date: Dec 2010
Posts: 393
|
Would this be appropriate? http://www.illumina.com/technology/g...ing_assay.ilmn
|
|
|
|
|
|
#3 | |
|
Senior Member
Location: UK Join Date: Jan 2010
Posts: 158
|
Quote:
http://www.ncbi.nlm.nih.gov/pubmed/18264105 |
|
|
|
|
![]() |
| Tags |
| hiseq, multiplexing |
| Thread Tools | |
|
|