groupCNVs-methods: Method 'groupCNVs'
In CNVrd2: CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data.
Description
Method groupCNVs
Methods
signature(Object = "clusteringCNVs")-
CNVrd2 documentation built on Nov. 8, 2020, 5:30 p.m.
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Description
Method groupCNVs
Methods
signature(Object = "clusteringCNVs")
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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