Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q42682842)
Watch
English
Multiple testing corrections for imputed SNPs
scientific article published on 19 January 2011
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
3055936
retrieved
4 November 2017
title
Multiple testing corrections for imputed SNPs
(English)
1 reference
stated in
Europe PubMed Central
PMCID
3055936
retrieved
4 November 2017
author name string
Xiaoyi Gao
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
3055936
retrieved
4 November 2017
publication date
19 January 2011
1 reference
stated in
Europe PubMed Central
PMCID
3055936
retrieved
4 November 2017
published in
Genetic Epidemiology
1 reference
stated in
Europe PubMed Central
PMCID
3055936
retrieved
4 November 2017
volume
35
1 reference
stated in
Europe PubMed Central
PMCID
3055936
retrieved
4 November 2017
page(s)
154-158
1 reference
stated in
Europe PubMed Central
PMCID
3055936
retrieved
4 November 2017
issue
3
1 reference
stated in
Europe PubMed Central
PMCID
3055936
retrieved
4 November 2017
cites work
Avoiding the high Bonferroni penalty in genome-wide association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
27 May 2018
Rapid and accurate multiple testing correction and power estimation for millions of correlated markers
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
27 May 2018
A groupwise association test for rare mutations using a weighted sum statistic
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
27 May 2018
Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
27 May 2018
PRESTO: rapid calculation of order statistic distributions and multiple-testing adjusted P-values via permutation for one and two-stage genetic association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
27 May 2018
Estimation of the multiple testing burden for genomewide association studies of nearly all common variants
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
27 May 2018
Estimation of significance thresholds for genomewide association scans
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
27 May 2018
Genome-wide significance for dense SNP and resequencing data
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
27 May 2018
So many correlated tests, so little time! Rapid adjustment of P values for multiple correlated tests
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
27 May 2018
PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
27 May 2018
Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
27 May 2018
A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
27 May 2018
The future of genetic studies of complex human diseases
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
27 May 2018
NHLBI Family Heart Study: objectives and design
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
27 May 2018
Empirical threshold values for quantitative trait mapping
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
27 May 2018
On multiple-testing correction in genome-wide association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
16 August 2018
A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
16 August 2018
A fast method for computing high-significance disease association in large population-based studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
16 August 2018
Rapid simulation of P values for product methods and multiple-testing adjustment in association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
16 August 2018
An efficient Monte Carlo approach to assessing statistical significance in genomic studies.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
16 August 2018
A simple correction for multiple comparisons in interval mapping genome scans.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3055936
retrieved
16 August 2018
Adjusting multiple testing in multilocus analyses using the eigenvalues of a correlation matrix
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGEPI.20563
retrieved
21 January 2018
Identifiers
DOI
10.1002/GEPI.20563
1 reference
stated in
Europe PubMed Central
PMCID
3055936
retrieved
4 November 2017
PMCID
3055936
1 reference
stated in
Europe PubMed Central
PMCID
3055936
retrieved
4 November 2017
PubMed ID
21254223
1 reference
stated in
Europe PubMed Central
PMCID
3055936
retrieved
4 November 2017
ResearchGate publication ID
49773700
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
