![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
Somatic Mutations in dbSNP | qqcandy | Bioinformatics | 14 | 07-27-2015 03:34 PM |
Pipeline to find somatic mutations | david.tamborero | Bioinformatics | 6 | 08-09-2013 03:05 AM |
Viewing of mutations with annotated genomic sequence | Robert Zagursky | Bioinformatics | 1 | 10-31-2011 09:13 AM |
WTSS, SQRL or RNA-seq | myrna | Literature Watch | 3 | 06-25-2011 08:40 AM |
mitochondrial mutations | honey | Bioinformatics | 0 | 06-10-2011 04:19 PM |
![]() |
|
Thread Tools |
![]() |
#1 |
Junior Member
Location: Netherlands Join Date: Dec 2010
Posts: 5
|
![]()
I'm a novel student bioinformatics and I am working on a transcriptome dataset of 4 cancer patients.
I've read a lot of articles about RNA-Seq. But none of the articles explains how many mutations you typically find in Rna sequencing of humans. I have a list of 5.000 mutations that occur in all the 4 patients at same position. (and more that only occurs in 1 or 2 patients) they spand 2000 known genes. dataset is alreay filtered for know Snp's Isn't that too much?? How many would you typically find ? Globally ? can't see the wood for trees Last edited by Stephanbio; 12-20-2010 at 05:17 AM. |
![]() |
![]() |
![]() |
#2 |
Senior Member
Location: Rochester, MN Join Date: Mar 2009
Posts: 191
|
![]()
That all depends on the pipeline you used. What is your protocol for generating this SNP list?
|
![]() |
![]() |
![]() |
Thread Tools | |
|
|