A comprehensive evaluation of SNP genotype imputation (Q34906095)

5 August 2017

A comprehensive evaluation of SNP genotype imputation (English)

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5 August 2017

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4

Michael Krawczak

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5 August 2017

3

Stefan Schreiber

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5 August 2017

5

Andre Franke

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5 August 2017

Michael Nothnagel

1

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5 August 2017

David Ellinghaus

series ordinal

2

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5 August 2017

17 December 2008

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5 August 2017

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5 August 2017

125

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5 August 2017

163-171

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5 August 2017

2

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https://scigraph.springernature.com/pub.10.1007/s00439-008-0606-5

5 August 2017

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cites work

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

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12 December 2020

PopGen: population-based recruitment of patients and controls for the analysis of complex genotype-phenotype relationships

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12 December 2020

A bias-ed assessment of the use of SNPs in human complex traits

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12 December 2020

A second generation human haplotype map of over 3.1 million SNPs

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12 December 2020

A haplotype map of the human genome

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Correlation between genetic and geographic structure in Europe

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12 December 2020

A statistical method for predicting classical HLA alleles from SNP data

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12 December 2020

Haploview: analysis and visualization of LD and haplotype maps

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12 December 2020

Sampling distribution of summary linkage disequilibrium measures

1 reference

12 December 2020

Analyses and comparison of accuracy of different genotype imputation methods

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12 December 2020

Handling missing values in population data: consequences for maximum likelihood estimation of haplotype frequencies

1 reference

12 December 2020

Ancient haplotypes of the HLA Class II region

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Human MHC architecture and evolution: implications for disease association studies

1 reference

12 December 2020

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

1 reference

12 December 2020

Maximum-likelihood estimation of haplotype frequencies in nuclear families

1 reference

12 December 2020

Haplotypic analysis of Wellcome Trust Case Control Consortium data

1 reference

12 December 2020

Patterns of linkage disequilibrium in the human genome

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12 December 2020

The International HapMap Project

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12 December 2020

10.1007/S00439-008-0606-5

Identifiers

DOI

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Dimensions Publication ID

5 August 2017

1038331739

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Fatcat ID

release_fpnmc2hxo5aajaczbvfj3yu4na

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Fatcat

https://api.fatcat.wiki/v0/release/fpnmc2hxo5aajaczbvfj3yu4na

24 November 2022

mapped directly with Wikidata item

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