sampleSniffer reads in all annotated VCF files in a directory, calculates the genetic distance between each pair of samples as number of SNP matches/total number of SNPS with valid values for both samples, then finds the closest genetic match for each sample.
Package details |
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Maintainer | |
License | CC0 |
Version | 0.0.0.9000 |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
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