Is there a tool that can output the raw genotype call (i.e., 0/1) rather than the actual basecall (A/T) from a VCF file?

Question: Is there a tool that can output the raw genotype call (i.e., 0/1) rather than the actual basecall (A/T) from a VCF file?

3.6 years ago by

mmats010 • 60

mmats010 • 60 wrote:

I'm interested in getting simple "heterozygous" or "homozygous" designations for all of the samples/SNPs in my multisample VCF file. In the past, I have been using the -GF GT option in GATK's VariantsToTable tool, and then annotating my basecalls in Excel as either heterozygous or homozygous. This takes forever since Excel isn't really built for big data like this. Is there a simple way to output all of the SNPs as 0/1, 0/0, 0/1, or 1/1 instead of C/A, A/A, G/T, C/C? My ideal output would be a txt file in a grid similar to how VariantsToTable outputs data: top row is each sample, while first column is the variant coordinates.

genotyping snp variantstotable gatk • 1.7k views

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modified 3.6 years ago by Jorge Amigo ♦ 11k • written 3.6 years ago by mmats010 • 60

Isn't that pretty close to how a vcf file naturally looks?

ADD REPLY • link written 3.6 years ago by swbarnes2 ♦ 7.8k

This takes forever since Excel isn't really built for big data like this.

That's a bit of an understatement. Good that you try to find an alternative!

ADD REPLY • link written 3.6 years ago by WouterDeCoster ♦ 43k

3.6 years ago by

Jorge Amigo ♦ 11k

Santiago de Compostela, Spain

Jorge Amigo ♦ 11k wrote:

if you start from a valid vcf file, you can get your desired output simply with this command:

grep -v ^## input.vcf | cut -f1,2,10- | sed 's/:\S*//g'

grep to remove all headers but column names, cut to select chromosome+position+samples' columns, and sed to remove everything but GT from genotype columns.

ADD COMMENT • link written 3.6 years ago by Jorge Amigo ♦ 11k

Thanks, this seems like the quickest method. I only worry because The Broad's documentation on generating tables from VCF files warns very sternly about not using a dedicated tool to parse out a VCF file

No, really, don't write your own parser if you can avoid it. This is not a comment on how smart or how competent we think you are -- it's a comment on how annoyingly obtuse and convoluted the VCF format is.

However, my VCF file seems valid and I dont see any weird outputs, so thanks again.

ADD REPLY • link written 3.6 years ago by mmats010 • 60

3.6 years ago by

WouterDeCoster ♦ 43k

Belgium

WouterDeCoster ♦ 43k wrote:

You are looking for a conversion to plink format, which you can do with VCFtools --plink, see this page

ADD COMMENT • link written 3.6 years ago by WouterDeCoster ♦ 43k

3.6 years ago by

harold.smith.tarheel • 4.5k

United States

harold.smith.tarheel • 4.5k wrote:

VCFtools and VCFlib support filtering by genotype.

ADD COMMENT • link modified 3.6 years ago • written 3.6 years ago by harold.smith.tarheel • 4.5k

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