(Q38121526)

29 August 2017

title

Genotype imputation in genome-wide association studies (English)

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genome-wide association study

29 August 2017

main subject

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Christian Fuchsberger

series ordinal

3

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29 August 2017

2

Serena Sanna

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Eleonora Porcu

series ordinal

1

object named as

Eleonora Porcu

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Lars G Fritsche

object named as

Lars G Fritsche

series ordinal

4

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publication date

1 July 2013

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Current protocols in human genetics / editorial board, Nicholas C, Dracapoli ... [et al.]

29 August 2017

published in

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29 August 2017

volume

Chapter 1

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29 August 2017

page(s)

Unit 1.25

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An integrated map of genetic variation from 1,092 human genomes

29 August 2017

cites work

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https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markers

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

Practical aspects of imputation-driven meta-analysis of genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

Genotype-imputation accuracy across worldwide human populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

Integrating common and rare genetic variation in diverse human populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

Complement factor H polymorphism in age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

Detection of sharing by descent, long-range phasing and haplotype imputation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

Siblings with ischemic stroke study: results of a genome-wide scan for stroke loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

Sequencing technologies - the next generation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

PLINK: a tool set for whole-genome association and population-based linkage analyses

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

Common variants in the GDF5-UQCC region are associated with variation in human height

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

The effect of genome-wide association scan quality control on imputation outcome for common variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

HAPGEN2: simulation of multiple disease SNPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

PEDSTATS: descriptive statistics, graphics and quality assessment for gene mapping data

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG0125S78

10.1002/0471142905.HG0125S78

21 January 2018

Identifiers

DOI

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29 August 2017

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