<div><p>Region-based association analysis is a more powerful tool for gene mapping than testing of individual genetic variants, particularly for rare genetic variants. The most powerful methods for regional mapping are based on the functional data analysis approach, which assumes that the regional genome of an individual may be considered as a continuous stochastic function that contains information about both linkage and linkage disequilibrium. Here, we extend this powerful approach, earlier applied only to independent samples, to the samples of related individuals. To this end, we additionally include a random polygene effects in functional linear model used for testing association between quantitative traits and multiple genetic variants...
Association studies offer an exciting approach to finding underlying genetic variants of complex hum...
Whilst thousands of genetic variants have been associated with human traits, identifying the subset ...
<p>Proportion of causal variants is the proportion of all rare variants (MAF ≤ 0.03) within the regi...
Genome-wide association analysis is an important approach to identify genetic variants associated wi...
Gene-based association testing with rare variants requires arbitrarily aggregating or collapsing the...
<p>Compared methods are the burden-based (famBT), kernel-based (famSKAT), optimized kernel-based (fa...
<div><p>Regional-based association analysis instead of individual testing of each SNP was introduced...
In genome-wide association studies (GWAS), efficient incorporation of linkage disequilibria (LD) amo...
Next-generation DNA sequencing platforms can effectively detect the entire spectrum of genomic varia...
Regional-based association analysis instead of individual testing of each SNP was introduced in geno...
While progress has been made in identifying common genetic variants associated with human diseases, ...
An individual's disease risk is determined by the compounded action of both common variants, inherit...
Access restricted to the OSU CommunityIn this dissertation, we develop statistical methods for analy...
An important problem in the final stage of positional cloning is to determine whether associated SNP...
Abstract We use the Genetic Analysis Workshop 14 simulated data to explore the effecti...
Association studies offer an exciting approach to finding underlying genetic variants of complex hum...
Whilst thousands of genetic variants have been associated with human traits, identifying the subset ...
<p>Proportion of causal variants is the proportion of all rare variants (MAF ≤ 0.03) within the regi...
Genome-wide association analysis is an important approach to identify genetic variants associated wi...
Gene-based association testing with rare variants requires arbitrarily aggregating or collapsing the...
<p>Compared methods are the burden-based (famBT), kernel-based (famSKAT), optimized kernel-based (fa...
<div><p>Regional-based association analysis instead of individual testing of each SNP was introduced...
In genome-wide association studies (GWAS), efficient incorporation of linkage disequilibria (LD) amo...
Next-generation DNA sequencing platforms can effectively detect the entire spectrum of genomic varia...
Regional-based association analysis instead of individual testing of each SNP was introduced in geno...
While progress has been made in identifying common genetic variants associated with human diseases, ...
An individual's disease risk is determined by the compounded action of both common variants, inherit...
Access restricted to the OSU CommunityIn this dissertation, we develop statistical methods for analy...
An important problem in the final stage of positional cloning is to determine whether associated SNP...
Abstract We use the Genetic Analysis Workshop 14 simulated data to explore the effecti...
Association studies offer an exciting approach to finding underlying genetic variants of complex hum...
Whilst thousands of genetic variants have been associated with human traits, identifying the subset ...
<p>Proportion of causal variants is the proportion of all rare variants (MAF ≤ 0.03) within the regi...