ArticleBMC genetics2010
Mapping haplotype-haplotype interactions with adaptive LASSO.
Article in BMC genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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Who cites it
12 citing papers in PubMed.
- Statistical Methods and Software for Substance Use and Dependence Genetic Research.Current genomics · 2019Review
- Exploring and Harnessing Haplotype Diversity to Improve Yield Stability in Crops.Frontiers in plant science · 2017Review
- A Three-Way Interaction among Maternal and Fetal Variants Contributing to Congenital Heart Defects.Annals of human genetics · 2016Article
- A penalized likelihood approach for investigating gene-drug interactions in pharmacogenetic studies.Biometrics · 2015Article
- Detecting epistasis in human complex traits.Nature reviews. Genetics · 2014Review
- A genetic association study detects haplotypes associated with obstructive heart defects.Human genetics · 2014Article
- Entropy-based selection for maternal-fetal genotype incompatibility with application to preterm prelabor rupture of membranes.BMC genetics · 2014Article
- Detecting maternal-fetal genotype interactions associated with conotruncal heart defects: a haplotype-based analysis with penalized logistic regression.Genetic epidemiology · 2014Article
- Epistatic effects on abdominal fat content in chickens: results from a genome-wide SNP-SNP interaction analysis.PloS one · 2013Article
- Wrapper-based selection of genetic features in genome-wide association studies through fast matrix operations.Algorithms for molecular biology : AMB · 2012Article
- Detecting genetic interactions for quantitative traits with U-statistics.Genetic epidemiology · 2011Article
- Systems biology data analysis methodology in pharmacogenomics.Pharmacogenomics · 2011Review
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Authors and funding
4 authors.
Funding
Abstract
backgroundThe genetic etiology of complex diseases in human has been commonly viewed as a complex process involving both genetic and environmental factors functioning in a complicated manner. Quite often the interactions among genetic variants play major roles in determining the susceptibility of an individual to a particular disease. Statistical methods for modeling interactions underlying complex diseases between single genetic variants (e.g. single nucleotide polymorphisms or SNPs) have been extensively studied. Recently, haplotype-based analysis has gained its popularity among genetic association studies. When multiple sequence or haplotype interactions are involved in determining an individual's susceptibility to a disease, it presents daunting challenges in statistical modeling and testing of the interaction effects, largely due to the complicated higher order epistatic complexity.
resultsIn this article, we propose a new strategy in modeling haplotype-haplotype interactions under the penalized logistic regression framework with adaptive L1-penalty. We consider interactions of sequence variants between haplotype blocks. The adaptive L1-penalty allows simultaneous effect estimation and variable selection in a single model. We propose a new parameter estimation method which estimates and selects parameters by the modified Gauss-Seidel method nested within the EM algorithm. Simulation studies show that it has low false positive rate and reasonable power in detecting haplotype interactions. The method is applied to test haplotype interactions involved in mother and offspring genome in a small for gestational age (SGA) neonates data set, and significant interactions between different genomes are detected.
conclusionsAs demonstrated by the simulation studies and real data analysis, the approach developed provides an efficient tool for the modeling and testing of haplotype interactions. The implementation of the method in R codes can be freely downloaded from http://www.stt.msu.edu/~cui/software.html.
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