Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets (Q35030986)

5 August 2017

Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets (English)

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5 August 2017

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Jeffrey C Barrett

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Katherine I. Morley

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Katherine I Morley

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author name string

Luke Jostins

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5 August 2017

2 March 2011

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European Journal of Human Genetics

5 August 2017

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5 August 2017

19

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5 August 2017

662-666

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5 August 2017

6

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https://scigraph.springernature.com/pub.10.1038/ejhg.2011.10

5 August 2017

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cites work

Integrating common and rare genetic variation in diverse human populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110048

Genotype imputation for genome-wide association studies

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110048

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110048

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110048

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110048

Genotype-imputation accuracy across worldwide human populations

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110048

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110048

Detecting shared pathogenesis from the shared genetics of immune-related diseases

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110048

A comprehensive evaluation of SNP genotype imputation

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110048

Evaluating the effects of imputation on the power, coverage, and cost efficiency of genome-wide SNP platforms

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110048

A second generation human haplotype map of over 3.1 million SNPs

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110048

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110048

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110048

Cohort profile: 1958 British birth cohort (National Child Development Study).

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110048

Evaluating coverage of genome-wide association studies

8 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2011.10

21 January 2018

Identifiers

DOI

10.1038/EJHG.2011.10

1 reference

5 August 2017

1 reference

5 August 2017

1 reference

PubMed ID

21364697