(Q34341329)

1 August 2017

title

Efficiency and power as a function of sequence coverage, SNP array density, and imputation (English)

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1 August 2017

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7

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1 August 2017

Jason Flannick

1

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1 August 2017

Joshua M Korn

2

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1 August 2017

Pierre Fontanillas

3

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1 August 2017

George B Grant

4

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1 August 2017

Eric Banks

5

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1 August 2017

Mark A Depristo

6

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1 August 2017

publication date

12 July 2012

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PLOS Computational Biology

1 August 2017

published in

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1 August 2017

volume

8

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1 August 2017

issue

7

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1 August 2017

page(s)

e1002604

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Creative Commons Attribution 4.0 International

1 August 2017

copyright license

start time

12 July 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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A window into third-generation sequencing

6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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Genetic heterogeneity in human disease

6 July 2018

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6 July 2018

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Rare variants create synthetic genome-wide associations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3395607

A composite of multiple signals distinguishes causal variants in regions of positive selection

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3395607

Sequencing technologies - the next generation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3395607

Simultaneous genotype calling and haplotype phasing improves genotype accuracy and reduces false-positive associations for genome-wide association studies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3395607

Finding the missing heritability of complex diseases

6 July 2018

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6 July 2018

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6 July 2018

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Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies

6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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A comprehensive evaluation of SNP genotype imputation

6 July 2018

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Practical issues in imputation-based association mapping

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3395607

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3395607

Calibrating the performance of SNP arrays for whole-genome association studies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3395607

Common and rare variants in multifactorial susceptibility to common diseases

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3395607

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3395607

A second generation human haplotype map of over 3.1 million SNPs

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3395607

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3395607

Power to detect risk alleles using genome-wide tag SNP panels

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3395607

A genotype calling algorithm for the Illumina BeadArray platform

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3395607

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3395607

Efficiency and power in genetic association studies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3395607

Deep sequencing reveals 50 novel genes for recessive cognitive disorders.

6 July 2018

1 reference

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https://api.crossref.org/works/10.1371%2FJOURNAL.PCBI.1002604

Evaluating coverage of genome-wide association studies

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PCBI.1002604

Evaluating and improving power in whole-genome association studies using fixed marker sets.

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PCBI.1002604

Transferability of tag SNPs to capture common genetic variation in DNA repair genes across multiple populations

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22807667

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PCBI.1002604

1 reference

journals/ploscb/FlannickKFGBDA12

1 August 2017

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

1 August 2017

1 reference