Title: | The subREgion-based BurdEn Test (REBET) |
---|---|
Description: | There is an increasing focus to investigate the association between rare variants and diseases. The REBET package implements the subREgion-based BurdEn Test which is a powerful burden test that simultaneously identifies susceptibility loci and sub-regions. |
Authors: | Bill Wheeler [cre], Bin Zhu [aut], Lisa Mirabello [ctb], Nilanjan Chatterjee [ctb] |
Maintainer: | Bill Wheeler <[email protected]> |
License: | GPL-2 |
Version: | 1.25.0 |
Built: | 2024-12-14 03:04:26 UTC |
Source: | https://github.com/bioc/REBET |
Data for the example.
The data contains a binary phenotype vector response
,
a genotype matrix genotypes
consisting of 20 rare-variant SNPs,
and the sub-region annotation vector subRegions
for the rebet
example.
data(data, package="REBET") # Display some of the data table(response) dim(genotypes) subRegions
data(data, package="REBET") # Display some of the data table(response) dim(genotypes) subRegions
A Subregion-based Burden Test for Simultaneous Identification of Susceptibility Loci and Sub-regions within
rebet(response, genotypes, subRegions, responseType=NULL, covariates=NULL, shape1=1, shape2=1, saveMem=FALSE)
rebet(response, genotypes, subRegions, responseType=NULL, covariates=NULL, shape1=1, shape2=1, saveMem=FALSE)
response |
Numerical vector of phenotypes. A binary phenotype must be coded as 0 and 1. |
genotypes |
Matrix of genotypes with each column as a locus. |
subRegions |
Sub-region annotation vector with length equal to the number of columns of |
responseType |
NULL, "continuous" or "binary".
If NULL, then "continuous" or "binary" will be chosen based on |
covariates |
NULL or matrix of covariates. The default is NULL. |
shape1 |
The |
shape2 |
The |
saveMem |
TRUE or FALSE to conserve memory (see details). The default is FALSE. |
See the reference for details of this method.
Missing values in any of response
, genotypes
or covariates
will be removed
before the analysis. Setting saveMem
to TRUE will allow for the
analysis of a much larger number of subjects, but will take more time to compute.
When saveMem
is FALSE, there needs to be enough memory available to hold
two or three NxN matrices, where N is the number of subjects.
This function calls the h.traits
function in the
ASSET
package.
The object returned from h.traits
in the
ASSET
package.
Bin Zhu <[email protected]>, Lisa Mirabello and Nilanjan Chatterjee
Zhu, B., Mirabello, L., Chatterjee, N. (2018) A Subregion-based Burden Test for Simultaneous Identification of Susceptibility Loci and Sub-regions within Genetic Epidemiology. In press. https://doi.org/10.1002/gepi.22134
data(data, package="REBET") res <- rebet(response, genotypes, subRegions) h.summary(res)
data(data, package="REBET") res <- rebet(response, genotypes, subRegions) h.summary(res)
An R package for the subREgion-based BurdEn Test (REBET).
In rare-variant association studies, aggregating rare and/or low frequency variants,
may increase statistical power for detection of the underlying susceptibility gene or region.
However, it is unclear which variants, or class of them, in a gene contribute most to the association.
This subregion-based burden test (REBET) simultaneously selects susceptibility genes and
identifies important underlying sub-regions.
The sub-regions are predefined based on shared common biologic characteristics,
such as the protein domain or possible functional impact.
Based on a subset-based approach considering local correlations between combinations
of test statistics of sub-regions, REBET is able to properly control the type I error rate
while adjusting for multiple comparisons in a computationally efficient manner.
See the reference for the details of this test.
The main function in this package is rebet
, which performs the REBET test.
Bin Zhu <[email protected]>, Lisa Mirabello and Nilanjan Chatterjee
Zhu, B., Mirabello, L., Chatterjee, N. (2018) A Subregion-based Burden Test for Simultaneous Identification of Susceptibility Loci and Sub-regions within Genetic Epidemiology. In press. https://doi.org/10.1002/gepi.22134