A comparison of approaches to account for uncertainty in analysis of imputed genotypes (Q35128434)

6 August 2017

A comparison of approaches to account for uncertainty in analysis of imputed genotypes (English)

1 reference

6 August 2017

3

1 reference

6 August 2017

Jin Zheng

1

1 reference

PubMed ID

21254217

6 August 2017

Yun Li

series ordinal

2

1 reference

PubMed ID

21254217

6 August 2017

Paul Scheet

series ordinal

4

1 reference

6 August 2017

1 February 2011

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6 August 2017

1 reference

6 August 2017

35

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6 August 2017

102-110

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6 August 2017

2

1 reference

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

6 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

Practical issues in imputation-based association mapping

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

Missing data imputation and haplotype phase inference for genome-wide association studies

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

Common variants near MC4R are associated with fat mass, weight and risk of obesity

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

Identification of ten loci associated with height highlights new biological pathways in human growth

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

A second generation human haplotype map of over 3.1 million SNPs

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

Imputation-based analysis of association studies: candidate regions and quantitative traits

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

Calibrating a coalescent simulation of human genome sequence variation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

Model-based inference of haplotype block variation.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3143715

A Simplex Method for Function Minimization

27 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FGEPI.20552

21 January 2018

Identifiers

DOI

10.1002/GEPI.20552

1 reference

6 August 2017

1 reference

6 August 2017

1 reference

PubMed ID

21254217