R: Risk Analysis of Genomic Copy Number Variation

# Risk Analysis of Genomic Copy Number Variation

## Documentation for package ‘RiskyCNV’ version 0.1.0

- DESCRIPTION file
- User guides, package vignettes and other documentation

## Help Pages

RiskyCNV-package | RiskyCNV: A General-Purpose CNV Analysis Workflow for Disease Risk Stratification
aberration | Detect Copy Number Aberrations (Gains and Losses)
annotate | Annotate CNV Regions with Gene Symbols
classify_risk | Classify Samples into Risk Categories
correlate_with_expr | Correlate CNV Profiles with Gene Expression Data
create_CNVMatrix | Create a CNV Expression Matrix
extract_metadata | Extract Sample Metadata and Classify into Grade or Stage Groups
recurrent | Identify Recurrent Copy Number Variations by Risk Group
RiskyCNV | RiskyCNV: A General-Purpose CNV Analysis Workflow for Disease Risk Stratification