Rapid and accurate multiple testing correction and power estimation for millions of correlated markers (Q33432685)

26 July 2017

Rapid and accurate multiple testing correction and power estimation for millions of correlated markers (English)

1 reference

26 July 2017

3

Eleazar Eskin

1 reference

26 July 2017

1

Buhm Han

1 reference

26 July 2017

Hyun Min Kang

2

1 reference

26 July 2017

17 April 2009

1 reference

26 July 2017

1 reference

26 July 2017

5

1 reference

26 July 2017

4

1 reference

26 July 2017

e1000456

1 reference

Creative Commons Attribution 4.0 International

26 July 2017

start time

17 April 2009

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Efficient association study design via power-optimized tag SNP selection

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PRESTO: rapid calculation of order statistic distributions and multiple-testing adjusted P-values via permutation for one and two-stage genetic association studies

14 July 2018

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Estimating coverage and power for genetic association studies using near-complete variation data

14 July 2018

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Increasing power in association studies by using linkage disequilibrium structure and molecular function as prior information

14 July 2018

1 reference

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Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

14 July 2018

1 reference

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Estimation of significance thresholds for genomewide association scans

14 July 2018

1 reference

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14 July 2018

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A second generation human haplotype map of over 3.1 million SNPs

14 July 2018

1 reference

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Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering

14 July 2018

1 reference

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Power analysis for genome-wide association studies

14 July 2018

1 reference

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PLINK: a tool set for whole-genome association and population-based linkage analyses

14 July 2018

1 reference

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A new multipoint method for genome-wide association studies by imputation of genotypes

14 July 2018

1 reference

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

14 July 2018

1 reference

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Leveraging the HapMap correlation structure in association studies

14 July 2018

1 reference

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Coverage and power in genomewide association studies

14 July 2018

1 reference

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A haplotype map of the human genome

14 July 2018

1 reference

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Inference and analysis of haplotypes from combined genotyping studies deposited in dbSNP

14 July 2018

1 reference

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Efficiency and power in genetic association studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663787

Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663787

A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663787

Statistical significance for genomewide studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663787

Score tests for association between traits and haplotypes when linkage phase is ambiguous

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663787

Linkage disequilibrium in humans: models and data

14 July 2018

1 reference

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Genomic control for association studies

14 July 2018

1 reference

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A DNA polymorphism discovery resource for research on human genetic variation

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663787

From genotypes to genes: doubling the sample size

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663787

The future of genetic studies of complex human diseases

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663787

A comparison of linkage disequilibrium measures for fine-scale mapping

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663787

On multiple-testing correction in genome-wide association studies

14 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000456

Rapid simulation of P values for product methods and multiple-testing adjustment in association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000456

An efficient Monte Carlo approach to assessing statistical significance in genomic studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000456

Testing untyped alleles (TUNA)-applications to genome-wide association studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000456

A simple correction for multiple comparisons in interval mapping genome scans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000456

A fast method for computing high-significance disease association in large population-based studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000456

Adjusting multiple testing in multilocus analyses using the eigenvalues of a correlation matrix

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663787

10.1371/JOURNAL.PGEN.1000456

31 October 2018

Identifiers

DOI

1 reference

26 July 2017

1 reference

26 July 2017

1 reference

PubMed ID

19381255