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Tools for efficient processing of large, whole genome genotype data sets in variant call format (VCF). It includes several functions to calculate commonly used population genomic metrics and a method for reference panel free genotype imputation, which is described in the preprint Gurke & Mayer (2024) <doi:10.22541/au.172515591.10119928/v1>.
Package details |
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Author | Marie Gurke [aut, cre] (<https://orcid.org/0000-0001-9901-424X>) |
Maintainer | Marie Gurke <margurke@gmail.com> |
License | GPL (>= 3) |
Version | 1.0.0 |
Package repository | View on CRAN |
Installation |
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