Large-scale genetic studies are often composed of related participants, and utilizing familial relationships can be cumbersome and computationally challenging. We present an approach to efficiently handle sequencing data from complex pedigrees that incorporates information from rare variants as well as common variants. Our method employs a 2-step procedure that sequentially regresses out correlation from familial relatedness and then uses the resulting phenotypic residuals in a penalized regression framework to test for associations with variants within genetic units. The operating characteristics of this approach are detailed using simulation data based on a large, multigenerational cohort
BACKGROUND: Feasibility of genotyping of hundreds and thousands of single nucleotide polymorphisms (...
© 2016 The Author(s). Both population-based and family-based designs are commonly used in genetic as...
Advances in high-throughput sequencing technologies are transforming the landscape of biomedical res...
Large-scale genetic studies are often composed of related participants, and utilizing familial relat...
An individual's disease risk is determined by the compounded action of both common variants, inherit...
An individual's disease risk is determined by the compounded action of both common variants, inherit...
Family based association studies are employed less often than case-control designs in the search for...
Complex human diseases are a major challenge for biological research. The goal of my research is to ...
Complex human diseases are a major challenge for biological research. The goal of my research is to ...
Complex human diseases are a major challenge for biological research. The goal of my research is to ...
Genome-wide association studies become increasingly popular and important for detecting genetic asso...
MOTIVATION: Next generation sequencing (NGS) technology considerably changed the way we screen for p...
Access restricted to the OSU CommunityIn this dissertation, we develop statistical methods for analy...
High-throughput sequencing studies (HTS) have been highly successful in identifying the genetic caus...
Recent advances in sequencing technologies have made it possible to explore the influence of rare va...
BACKGROUND: Feasibility of genotyping of hundreds and thousands of single nucleotide polymorphisms (...
© 2016 The Author(s). Both population-based and family-based designs are commonly used in genetic as...
Advances in high-throughput sequencing technologies are transforming the landscape of biomedical res...
Large-scale genetic studies are often composed of related participants, and utilizing familial relat...
An individual's disease risk is determined by the compounded action of both common variants, inherit...
An individual's disease risk is determined by the compounded action of both common variants, inherit...
Family based association studies are employed less often than case-control designs in the search for...
Complex human diseases are a major challenge for biological research. The goal of my research is to ...
Complex human diseases are a major challenge for biological research. The goal of my research is to ...
Complex human diseases are a major challenge for biological research. The goal of my research is to ...
Genome-wide association studies become increasingly popular and important for detecting genetic asso...
MOTIVATION: Next generation sequencing (NGS) technology considerably changed the way we screen for p...
Access restricted to the OSU CommunityIn this dissertation, we develop statistical methods for analy...
High-throughput sequencing studies (HTS) have been highly successful in identifying the genetic caus...
Recent advances in sequencing technologies have made it possible to explore the influence of rare va...
BACKGROUND: Feasibility of genotyping of hundreds and thousands of single nucleotide polymorphisms (...
© 2016 The Author(s). Both population-based and family-based designs are commonly used in genetic as...
Advances in high-throughput sequencing technologies are transforming the landscape of biomedical res...