![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
CNV-seq, to detect Copy Number Variation using next-generation sequencing | xiechao | Literature Watch | 46 | 10-20-2015 10:30 AM |
Bioinformatician High-Throughput Sequencing - Norwegian Sequencing Centre | tim | Academic/Non-Profit Jobs | 0 | 06-22-2011 09:47 AM |
PubMed: The edited transcriptome: novel high throughput approaches to detect nucleoti | Newsbot! | Literature Watch | 0 | 05-17-2011 03:10 AM |
Workshop: Informatics on High Throughput Sequencing | strob | Events / Conferences | 1 | 04-14-2009 08:21 PM |
How to detect real deletion or gaps in sequencing projects | watashi | Bioinformatics | 0 | 08-01-2008 02:15 PM |
![]() |
|
Thread Tools |
![]() |
#1 |
Member
Location: shanghai of china Join Date: May 2009
Posts: 29
|
![]()
i am doing rna editing analysis using solexa data,
i wann know which base is a I detected as ? even though it's translated as G in vivo thanks |
![]() |
![]() |
![]() |
#2 |
Member
Location: Dublin, Ireland Join Date: Mar 2008
Posts: 55
|
![]()
I'm not sure if I understand your question, however for detection of A to I RNA editing you need to sequence both the genomic DNA and RNA. If editing occurs you will only see an "A" in the DNA sequence but at the same genomic position in the cDNA (RNA) you will see both As and Gs.
Have a look at this publication for more info: "Genome-wide identification of human RNA editing sites by parallel DNA capturing and sequencing" Science. 2009 May 29;324(5931):1210-3. |
![]() |
![]() |
![]() |
#3 |
Member
Location: shanghai of china Join Date: May 2009
Posts: 29
|
![]()
OK,thanks for you reply and sorry for my english
![]() i understand ~~ |
![]() |
![]() |
![]() |
Thread Tools | |
|
|