Springer Nature
Browse
12864_2020_6627_MOESM4_ESM.docx (13.93 kB)

Additional file 4 of Concordance rate between copy number variants detected using either high- or medium-density single nucleotide polymorphism genotype panels and the potential of imputing copy number variants from flanking high density single nucleotide polymorphism haplotypes in cattle

Download (13.93 kB)
journal contribution
posted on 2020-03-05, 05:01 authored by Pierce Rafter, Isobel Gormley, Andrew Parnell, John Kearney, Donagh Berry
Additional file 4: Table S2. The location and population frequency of CNVs with an accuracy of at least 85% within at least one of the three breeds. The population frequency is the number of times the CNV was present in the total population, i.e. the reference and validation population. The accuracy, given as a percentage, is the number of times the CNV was accurately imputed divided by the number of times that CNV was called in the validation population. Where an accuracy of NA is reported, imputation was not undertaken for that CNV in that breed.

Funding

Science Foundation Ireland

History

Usage metrics

    BMC Genomics

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC