(Q33380176)

26 July 2017

Analyses and comparison of accuracy of different genotype imputation methods (English)

1 reference

26 July 2017

1 reference

Hong-Wen Deng

5

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author name string

Yu-Fang Pei

1

1 reference

26 July 2017

Jian Li

2

1 reference

26 July 2017

Lei Zhang

3

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26 July 2017

Christopher J Papasian

4

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26 July 2017

language of work or name

English

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publication date

29 October 2008

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26 July 2017

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26 July 2017

3

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26 July 2017

e3551

1 reference

26 July 2017

10

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Creative Commons Attribution 4.0 International

26 July 2017

start time

29 October 2008

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia

21 June 2018

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

21 June 2018

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

21 June 2018

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Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.

21 June 2018

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A second generation human haplotype map of over 3.1 million SNPs

21 June 2018

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

21 June 2018

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Methods to impute missing genotypes for population data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569208

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

21 June 2018

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

21 June 2018

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Evaluation of genome-wide power of genetic association studies based on empirical data from the HapMap project

21 June 2018

1 reference

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

21 June 2018

1 reference

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

21 June 2018

1 reference

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A worldwide survey of haplotype variation and linkage disequilibrium in the human genome

21 June 2018

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

21 June 2018

1 reference

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A comparison of phasing algorithms for trios and unrelated individuals

21 June 2018

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A haplotype map of the human genome

21 June 2018

1 reference

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Calibrating a coalescent simulation of human genome sequence variation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569208

Efficiency and power in genetic association studies

21 June 2018

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GERBIL: Genotype resolution and block identification using likelihood

21 June 2018

1 reference

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A comparison of bayesian methods for haplotype reconstruction from population genotype data

21 June 2018

1 reference

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A high-resolution recombination map of the human genome

21 June 2018

1 reference

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A New Statistical Method for Haplotype Reconstruction from Population Data

21 June 2018

1 reference

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Singular value decomposition for genome-wide expression data processing and modeling

21 June 2018

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Model-based inference of haplotype block variation.

21 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0003551

Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0003551

A new look at the statistical model identification

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0003551

10.1371/JOURNAL.PONE.0003551

21 January 2018

Identifiers

DOI

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26 July 2017

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26 July 2017

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