This image facilitates the usage of VCFtools, a program package designed for working with VCF files. The aim of VCFtools is to provide easily accessible methods for working with complex genetic variation data in the form of VCF files.
This toolset can be used to perform the following operations on VCF files:
Frequently used tools in this suite are:
To obtain the help of an application, you just need to run: docker run --rm bioinfoipec/vcftools <vcftools-application-name> --help (e.g. docker run --rm bioinfoipec/vcftools vcftools --help)
To run a package, you should adapt and run the following command: docker run --rm -v /your/data/dir:/data bioinfoipec/vcftools <vcftools-application-name> <options>
In this command, you should replace:
/your/data/dir to point to the directory that contains the input files you want to analyze.<vcftools-application-name> to the name of the VCFtools application you want to use.<options> with the specific options of the VCFtools application. These options will include the input/output files, which should be referenced under /data/.For instance, to output a new VCF file from the input VCF file that removes any indel sites, you should run: docker run --rm -v /your/data/dir:/data bioinfoipec/vcftools vcftools --gzvcf /data/ALL.chrY.phase3_integrated_v2a.20130502.genotypes.vcf.gz --remove-indels --recode --recode-INFO-all --out /data/output
To test the previous command, the dataset used is available here.
Content type
Image
Digest
Size
195 MB
Last updated
over 5 years ago
docker pull bioinfoipec/vcftools