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Detect Copy Number Variants from SNPs Data
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English
rCNV
Detect Copy Number Variants from SNPs Data

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    1.1.0
    26 October 2022
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    1.0.0
    6 April 2022
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    1.2.0
    8 August 2023
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    8 August 2023
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    Functions in this package will import filtered variant call format (VCF) files of SNPs data and generate data sets to detect copy number variants, visualize them and do downstream analyses with copy number variants(e.g. Environmental association analyses).
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