[[abstract]]We present a model-free approach to the study of the number of false discoveries for large-scale simultaneous family-based association tests (FBATs) in which the set of discoveries is decided by applying a threshold to the test statistics. When the association between a set of markers in a candidate gene and a group of phenotypes is studied by a class of FBATs, we indicate that a joint null hypothesis distribution for these statistics can be obtained by the fundamental statistical method of conditioning on sufficient statistics for the null hypothesis. Based on the joint null distribution of these statistics, we can obtain the distribution of the number of false discoveries for the set of discoveries defined by a threshold; the ...
With the development of sequencing technologies, the direct testing of rare variant associations has...
Case-control studies of genetic polymorphisms and gene-environment interactions are reporting large ...
Motivation: The question of how to best use information from known associated variants when conducti...
[[abstract]]We present a model-free approach to the study of the number of false discoveries for lar...
Background/Aims: We consider the situation that multiple genetic variants are underlying a heritable...
Abstract In a genome-wide association study, association between disease trait and hun...
Genetic association studies routinely involve massive numbers of statistical tests accompanied by P-...
<div><p>Genome-wide association studies (GWAS) have been successful in identifying single nucleotide...
The issue of large-scale testing has caught much attention with the advent of high-throughput techno...
For genetic association studies with multiple phenotypes, we propose a new strategy for multiple tes...
For genetic association studies with multiple phenotypes, we propose a new strategy for multiple tes...
Genome-wide association studies (GWAS) have been successful in identifying single nucleotide polymor...
For genetic association studies with multiple phenotypes, we propose a new strategy for multiple tes...
Multiple hypothesis testing is a fundamental problem in high dimensional inference, with wide applic...
Large-scale genetic association studies are increasingly utilized for identifying novel susceptible ...
With the development of sequencing technologies, the direct testing of rare variant associations has...
Case-control studies of genetic polymorphisms and gene-environment interactions are reporting large ...
Motivation: The question of how to best use information from known associated variants when conducti...
[[abstract]]We present a model-free approach to the study of the number of false discoveries for lar...
Background/Aims: We consider the situation that multiple genetic variants are underlying a heritable...
Abstract In a genome-wide association study, association between disease trait and hun...
Genetic association studies routinely involve massive numbers of statistical tests accompanied by P-...
<div><p>Genome-wide association studies (GWAS) have been successful in identifying single nucleotide...
The issue of large-scale testing has caught much attention with the advent of high-throughput techno...
For genetic association studies with multiple phenotypes, we propose a new strategy for multiple tes...
For genetic association studies with multiple phenotypes, we propose a new strategy for multiple tes...
Genome-wide association studies (GWAS) have been successful in identifying single nucleotide polymor...
For genetic association studies with multiple phenotypes, we propose a new strategy for multiple tes...
Multiple hypothesis testing is a fundamental problem in high dimensional inference, with wide applic...
Large-scale genetic association studies are increasingly utilized for identifying novel susceptible ...
With the development of sequencing technologies, the direct testing of rare variant associations has...
Case-control studies of genetic polymorphisms and gene-environment interactions are reporting large ...
Motivation: The question of how to best use information from known associated variants when conducti...