High-throughput DNA sequencing allows for the genotyping of common and rare variants for genetic association studies. At the present time and for the foreseeable future, it is not economically feasible to sequence all individuals in a large cohort. A cost-effective strategy is to sequence those individuals with extreme values of a quantitative trait. We consider the design under which the sampling depends on multiple quantitative traits. Under such trait-dependent sampling, standard linear regression analysis can result in bias of parameter estimation, inflation of type I error, and loss of power. We construct a likelihood function that properly reflects the sampling mechanism and utilizes all available data. We implement a computationally ...
<div><p></p><p>Owing to recent advances in DNA sequencing, it is now technically feasible to evaluat...
University of Minnesota Ph.D. dissertation. August 2013. Major: Biostatistics. Advisor: Wei Pan. 1 c...
Genome-wide association studies (GWAS) have successfully identified thousands of risk loci for compl...
High-throughput DNA sequencing allows for the genotyping of common and rare variants for genetic ass...
It is not economically feasible to sequence all study subjects in a large cohort. A cost-effective s...
Abstract Use of trait-dependent sampling designs in whole-genome association studies o...
High-throughput DNA sequencing provides an unprecedented opportunity to discover rare genetic varian...
Recent advances in sequencing technologies have made it possible to explore the influence of rare va...
Sequencing studies are increasingly being conducted to identify rare variants associated with comple...
Sequencing studies are increasingly being conducted to identify rare variants associated with comple...
Background—Genome-wide association studies have identified thousands of genetic variants that influe...
Sequencing studies are increasingly being conducted to identify rare variants associated with comple...
Owing to recent advances in DNA sequencing, it is now technically feasible to evaluate the contribut...
Deep sequencing will soon generate comprehensive sequence information in large disease samples. Alth...
Genome and exome sequencing in large cohorts enables characterization of the role of rare variation ...
<div><p></p><p>Owing to recent advances in DNA sequencing, it is now technically feasible to evaluat...
University of Minnesota Ph.D. dissertation. August 2013. Major: Biostatistics. Advisor: Wei Pan. 1 c...
Genome-wide association studies (GWAS) have successfully identified thousands of risk loci for compl...
High-throughput DNA sequencing allows for the genotyping of common and rare variants for genetic ass...
It is not economically feasible to sequence all study subjects in a large cohort. A cost-effective s...
Abstract Use of trait-dependent sampling designs in whole-genome association studies o...
High-throughput DNA sequencing provides an unprecedented opportunity to discover rare genetic varian...
Recent advances in sequencing technologies have made it possible to explore the influence of rare va...
Sequencing studies are increasingly being conducted to identify rare variants associated with comple...
Sequencing studies are increasingly being conducted to identify rare variants associated with comple...
Background—Genome-wide association studies have identified thousands of genetic variants that influe...
Sequencing studies are increasingly being conducted to identify rare variants associated with comple...
Owing to recent advances in DNA sequencing, it is now technically feasible to evaluate the contribut...
Deep sequencing will soon generate comprehensive sequence information in large disease samples. Alth...
Genome and exome sequencing in large cohorts enables characterization of the role of rare variation ...
<div><p></p><p>Owing to recent advances in DNA sequencing, it is now technically feasible to evaluat...
University of Minnesota Ph.D. dissertation. August 2013. Major: Biostatistics. Advisor: Wei Pan. 1 c...
Genome-wide association studies (GWAS) have successfully identified thousands of risk loci for compl...