![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
Calculating p-values from FPKM? | Artur Jaroszewicz | Bioinformatics | 16 | 10-25-2012 01:04 PM |
Calculating capture efficiency | T199Y | Bioinformatics | 3 | 11-08-2011 11:09 AM |
Gene list for calculating coverage | nseh | Bioinformatics | 1 | 05-22-2011 07:31 AM |
Calculating read lengths - SOLiD | naluru | SOLiD | 1 | 01-26-2011 05:57 AM |
calculating expected reads | Seqasaurus | 454 Pyrosequencing | 2 | 09-08-2010 04:27 AM |
![]() |
|
Thread Tools |
![]() |
#1 |
Member
Location: Seoul Join Date: Jan 2012
Posts: 42
|
![]()
as same as the title.
I'm NGS newbie and finding a useful tool for calculating coverage. the story of experiment is like this; capture all exons(no intron included!) of several genes(about 20) in human. What i'm doing is very primitive... seeing the bam file by samtools or IGV and confirm there result by eye and hand... the exons are apart and about 20 genes -> there are about a few hundred regions to check... please help me!!! |
![]() |
![]() |
![]() |
#2 |
Senior Member
Location: East Coast USA Join Date: Feb 2008
Posts: 7,088
|
![]()
Check this thread: http://seqanswers.com/forums/showthr...t=coverage+bam
|
![]() |
![]() |
![]() |
#3 |
Member
Location: Seoul Join Date: Jan 2012
Posts: 42
|
![]()
Thankyou
![]() |
![]() |
![]() |
![]() |
Thread Tools | |
|
|