CorDiff
CorDiff tests equality of covariance matrices across genomic features to detect changes in covariance associated with discrete or continuous experimental variables and to study genetic interactions.
Key Features:
- Uniform Framework: Tests associations between covariance matrices and an experimental variable, extending beyond two-sample problems and restrictive p versus n assumptions.
- Summary Statistics: Implements four distinct summary statistics tailored to detect different types of changes in covariance.
- Connectivity Statistic: Includes a connectivity statistic sensitive to global changes in covariance magnitude.
- Risk Score Association: Associates a natural individual risk score with several statistics for continuous experimental variables.
- Asymptotic Results: Provides asymptotic inference valid for continuous and discrete responses under mild conditions, including settings where the number of features (p) may exceed the sample size (n).
- Permutational Equivalence: Demonstrates permutational equivalence of the proposed statistics to some existing methods in specific two-sample cases.
Scientific Applications:
- Differential Covariance Analysis: Detects changes in covariance structure among genomic features across experimental conditions.
- High-Dimensional Genomics: Applies to large-scale genetic datasets where the number of features (p) can exceed sample size (n).
- Genetic Interaction Studies: Explores associations between covariance patterns and discrete or continuous experimental variables to inform studies of genetic interactions.
Methodology:
Performs covariance regression and computes four summary statistics including a connectivity statistic, employs asymptotic inference applicable when p may exceed n, and reports permutational equivalence results in two-sample cases.
Topics
Details
- License:
- GPL-2.0
- Programming Languages:
- R
- Added:
- 1/14/2020
- Last Updated:
- 12/16/2020
Operations
Publications
Zhou Y. Set‐based differential covariance testing for genomics. Stat. 2019;8(1). doi:10.1002/sta4.235. PMID:31763041. PMCID:PMC6853199.
DOI: 10.1002/STA4.235
PMID: 31763041
PMCID: PMC6853199
Funding: - National Human Genome Research Institute: CFF KNOWLE18XX0, R01HG009125, R21HG007840