Contemporary genetic association studies may test hundreds of thousands of genetic variants for association, often with multiple binary and continuous traits or under more than one model of inheritance. Many of these association tests may be correlated with one another because of linkage disequilibrium between nearby markers and correlation between traits and models. Permutation tests and simulation-based methods are often employed to adjust groups of correlated tests for multiple testing, since conventional methods such as Bonferroni correction are overly conservative when tests are correlated. We present here a method of computing P values adjusted for correlated tests (PACT) that attains the accuracy of permutation or simulation-based te...
Genome-wide association studies commonly involve simultaneous tests of millions of single nucleotide...
Background As we enter an era when testing millions of SNPs in a single gene association study will ...
Haplotypes—that is, linear arrangements of alleles on the same chromosome that were inherited as a u...
Contemporary genetic association studies may test hundreds of thousands of genetic variants for asso...
Contemporary genetic association studies may test hundreds of thousands of genetic variants for asso...
With the development of high-throughput sequencing and genotyping technologies, the number of marker...
We study exact tests for (2 x 2) and (2 x 3) contingency tables, in particular exact chi-squared tes...
Large exploratory studies, including candidate-gene–association testing, genomewide linkage-disequil...
Because of rapid progress in genotyping techniques, many large-scale, genomewide disease-association...
A major challenge in genome-wide association studies (GWASs) is to derive the multiple testing thres...
The interpretation of the results of large association studies encompassing much or all of the human...
We study exact tests for (2 x 2) and (2 x 3) contingency tables, in particular exact chi-squared tes...
Resolving the interplay of the genetic components of a complex disease is a challenging endeavor. Ov...
Methods for multiple-testing correction in local expression quantitative trait locus (cis-eQTL) stud...
Correlated multiple testing is widely performed in genetic research, particularly in multilocus anal...
Genome-wide association studies commonly involve simultaneous tests of millions of single nucleotide...
Background As we enter an era when testing millions of SNPs in a single gene association study will ...
Haplotypes—that is, linear arrangements of alleles on the same chromosome that were inherited as a u...
Contemporary genetic association studies may test hundreds of thousands of genetic variants for asso...
Contemporary genetic association studies may test hundreds of thousands of genetic variants for asso...
With the development of high-throughput sequencing and genotyping technologies, the number of marker...
We study exact tests for (2 x 2) and (2 x 3) contingency tables, in particular exact chi-squared tes...
Large exploratory studies, including candidate-gene–association testing, genomewide linkage-disequil...
Because of rapid progress in genotyping techniques, many large-scale, genomewide disease-association...
A major challenge in genome-wide association studies (GWASs) is to derive the multiple testing thres...
The interpretation of the results of large association studies encompassing much or all of the human...
We study exact tests for (2 x 2) and (2 x 3) contingency tables, in particular exact chi-squared tes...
Resolving the interplay of the genetic components of a complex disease is a challenging endeavor. Ov...
Methods for multiple-testing correction in local expression quantitative trait locus (cis-eQTL) stud...
Correlated multiple testing is widely performed in genetic research, particularly in multilocus anal...
Genome-wide association studies commonly involve simultaneous tests of millions of single nucleotide...
Background As we enter an era when testing millions of SNPs in a single gene association study will ...
Haplotypes—that is, linear arrangements of alleles on the same chromosome that were inherited as a u...