Empirical Bayes scan statistics for detecting clusters of disease risk variants in genetic studies
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Publication:2809542
DOI10.1111/BIOM.12331zbMATH Open1419.62406OpenAlexW1767978978WikidataQ40879974 ScholiaQ40879974MaRDI QIDQ2809542FDOQ2809542
Authors: Kenneth J. McCallum, Iuliana Ionita-Laza 
Publication date: 30 May 2016
Published in: Biometrics (Search for Journal in Brave)
Full work available at URL: http://europepmc.org/articles/pmc4666841
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Cited In (13)
- An empirical Bayes risk prediction model using multiple traits for sequencing data
- A weighted empirical Bayes risk prediction model using multiple traits
- An empirical Bayes testing procedure for detecting variants in analysis of next generation sequencing data
- Covariance-based sample selection for heterogeneous data: applications to gene expression and autism risk gene detection
- Simultaneous Detection of Signal Regions Using Quadratic Scan Statistics With Applications to Whole Genome Association Studies
- A Bayesian clustering approach for detecting gene-gene interactions in high-dimensional genotype data
- Modeling the Association Between Clusters of SNPs and Disease Responses
- Wavelet-based genetic association analysis of functional phenotypes arising from high-throughput sequencing assays
- A Bayes factor approach with informative prior for rare genetic variant analysis from next generation sequencing data
- Fast implementation of a scan statistic for identifying chromosomal patterns of genome wide association studies
- Network assisted analysis to reveal the genetic basis of autism
- A new structural approach to genomic discovery of disease: example of adult-onset diabetes
- Efficient identification of context dependent subgroups of risk from genome-wide association studies
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