(Q34177177)

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Two-stage study designs combining genome-wide association studies, tag single-nucleotide polymorphisms, and exome sequencing: accuracy of genetic effect estimates

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Two-stage study designs combining genome-wide association studies, tag single-nucleotide polymorphisms, and exome sequencing: accuracy of genetic effect estimates (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

genome-wide association study

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single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

author name string

Laura L Faye

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Shelley B Bull

2

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Europe PubMed Central

PubMed publication ID

31 July 2017

publication date

29 November 2011

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Europe PubMed Central

PubMed publication ID

31 July 2017

BMC Proceedings

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Europe PubMed Central

PubMed publication ID

31 July 2017

5 Suppl 9

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Europe PubMed Central

PubMed publication ID

31 July 2017

S64

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Europe PubMed Central

PubMed publication ID

31 July 2017

copyright license

Creative Commons Attribution 2.0 Generic

29 November 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Genetic Analysis Workshop 17 mini-exome simulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287903

5 July 2018

Statistical analysis of rare sequence variants: an overview of collapsing methods

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287903

5 July 2018

BR-squared: a practical solution to the winner's curse in genome-wide scans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287903

5 July 2018

Rare variants create synthetic genome-wide associations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287903

5 July 2018

An evaluation of statistical approaches to rare variant analysis in genetic association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287903

5 July 2018

A second generation human haplotype map of over 3.1 million SNPs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287903

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287903

5 July 2018

Large upward bias in estimation of locus-specific effects from genomewide scans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287903

5 July 2018

Upward bias in odds ratio estimates from genome-wide association studies

1 reference

https://api.crossref.org/works/10.1186%2F1753-6561-5-S9-S64

21 January 2018

A flexible genome-wide bootstrap method that accounts for ranking and threshold-selection bias in GWAS interpretation and replication study design.

1 reference

https://api.crossref.org/works/10.1186%2F1753-6561-5-S9-S64

21 January 2018

Identifiers

10.1186/1753-6561-5-S9-S64

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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