rCNV (Q92014)
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Detect Copy Number Variants from SNPs Data
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | No label defined |
||
| English | rCNV |
Detect Copy Number Variants from SNPs Data |
Statements
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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