This package contains a set of functions to perform several type of processing and analysis on CNVs calling pipelines/algorithms results in an integrated manner and regardless of the raw data type (SNPs array or NGS). It provides functions to combine multiple CNV calling results into a single object, filter them, compute CNVRs (CNV Regions) and inheritance patterns, detect genic load, and more. The package is best suited for studies in human family-based cohorts.
Package details |
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Bioconductor views | Preprocessing Software WorkflowStep |
Maintainer | |
License | GPL-3 |
Version | 0.99.15 |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
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