![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
GATK UnifiedGenotyper not calling any variants | krobasky | Bioinformatics | 7 | 10-25-2012 11:19 PM |
Do you size select?? | James | Sample Prep / Library Generation | 6 | 05-17-2011 06:36 PM |
Sure Select on Illumina.... | VanessaS | Sample Prep / Library Generation | 1 | 02-04-2011 09:06 AM |
Agilent Sure Select | athos | Illumina/Solexa | 2 | 01-28-2011 01:47 PM |
Sure Select Exon Capture | manisisland | Genomic Resequencing | 3 | 12-21-2010 03:59 PM |
![]() |
|
Thread Tools |
![]() |
#1 |
Member
Location: Planet Earth Join Date: Jan 2011
Posts: 26
|
![]()
Hi,
assume I have 2 .vcf files from 2 individual samples which I would like to combine with GATK CombineVariants function. Then I would like to filter in a way that I end up only with variants that are present in both samples e.g. through GATK SelectVariants function. Or is there a better way ? Can anyone tell me how to do this ? Thanx ! |
![]() |
![]() |
![]() |
#2 |
Senior Member
Location: San Diego Join Date: May 2008
Posts: 912
|
![]()
BEDTools can take vcfs as input, and output the overlap. Or the ones that don't overlap.
|
![]() |
![]() |
![]() |
#3 |
Member
Location: Planet Earth Join Date: Jan 2011
Posts: 26
|
![]()
Oh, of course - thanks for bringing me on track again! :=)
|
![]() |
![]() |
![]() |
Thread Tools | |
|
|