Estimating genome-wide significance for whole-genome sequencing studies (Q41486298)

1 October 2017

Estimating genome-wide significance for whole-genome sequencing studies (English)

1 reference

1 October 2017

whole genome sequencing

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24676807%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

Eleftheria Zeggini

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24676807%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

Celia Greenwood

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24676807%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

author name string

ChangJiang Xu

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24676807%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

Ioanna Tachmazidou

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24676807%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

Antonio Ciampi

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24676807%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

UK10K Consortium

7

1 reference

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11 June 2020

publication date

14 February 2014

1 reference

1 October 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24676807%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

volume

38

1 reference

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11 June 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24676807%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

page(s)

281-290

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24676807%20AND%20SRC:MED&resulttype=core&format=json

Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation

11 June 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489336

Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489336

Evaluating the effective numbers of independent tests and significant p-value thresholds in commercial genotyping arrays and public imputation reference datasets

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489336

A new approach to account for the correlations among single nucleotide polymorphisms in genome: wide association studies

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489336

Rare-variant association testing for sequencing data with the sequence kernel association test

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489336

Pooled association tests for rare variants in exon-resequencing studies

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489336

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

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489336

Estimation of significance thresholds for genomewide association scans

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489336

Population structure and eigenanalysis

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489336

On multiple-testing correction in genome-wide association studies

11 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489336

A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489336

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

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4489336

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

19 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FGEPI.21797

Effect of genome-wide genotyping and reference panels on rare variants imputation

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24676807

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/GEPI.21797

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24676807%20AND%20SRC:MED&resulttype=core&format=json

release_r44pmjanhfa2ncn5mh6mgdnp4y

11 June 2020

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/r44pmjanhfa2ncn5mh6mgdnp4y

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24676807%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24676807%20AND%20SRC:MED&resulttype=core&format=json