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Hello,
my data is in VCF. However, it seems like I need plink format to be able to get genotype matrix as well as defining SNP sets... is there a way I can use VCF file and be able to define the collapsing region?
Thanks
Andreanne
Seunggeun (Shawn) Lee
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Feb 16, 2014, 10:08:19 PM2/16/14
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Hi Andreanne,
There is a R package "SeqMiner" (http://zhanxw.com/vcf2geno/) that can be used to read VCF file. I used it several times, and it works very well.
Thanks,
Shawn
freeseek
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Mar 25, 2014, 11:40:02 AM3/25/14
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You can also use plink2 (https://www.cog-genomics.org/plink2/) to convert your VCF file to a plink format you can load with SKAT. The conversion is really fast.