Utilizing genotype imputation for the augmentation of sequence data (Q33603074)

28 July 2017

title

Utilizing genotype imputation for the augmentation of sequence data (English)

1 reference

28 July 2017

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Robert Freimuth

5

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Brooke L Fridley

series ordinal

1

object named as

Brooke L Fridley

1 reference

28 July 2017

Gregory Jenkins

2

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28 July 2017

Matthew E Deyo-Svendsen

series ordinal

3

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28 July 2017

Scott Hebbring

series ordinal

4

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28 July 2017

language of work or name

English

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publication date

8 June 2010

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28 July 2017

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28 July 2017

volume

5

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28 July 2017

issue

6

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28 July 2017

page(s)

e11018

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Creative Commons Attribution 4.0 International

28 July 2017

copyright license

start time

8 June 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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

1 reference

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

21 June 2018

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Validating, augmenting and refining genome-wide association signals

21 June 2018

1 reference

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Genotype-imputation accuracy across worldwide human populations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2882389

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2882389

A comprehensive evaluation of SNP genotype imputation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2882389

Analyses and comparison of accuracy of different genotype imputation methods

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2882389

Next-generation DNA sequencing

21 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2882389

Imputing missing genotypic data of single-nucleotide polymorphisms using neural networks

21 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2882389

Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms

21 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2882389

A second generation human haplotype map of over 3.1 million SNPs

21 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2882389

Mixed modeling and multiple imputation for unobservable genotype clusters

21 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2882389

Methods to impute missing genotypes for population data

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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Inferring missing genotypes in large SNP panels using fast nearest-neighbor searches over sliding windows

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2882389

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

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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Haploview: analysis and visualization of LD and haplotype maps

21 June 2018

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Imputation methods to improve inference in SNP association studies

21 June 2018

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Crossref

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0011018

Testing untyped alleles (TUNA)-applications to genome-wide association studies

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0011018

1000 Genomes Project promises closer look at variation in human genome

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20543988

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0011018

1 reference

release_jzf76zst2zfjriferjvd3rysf4

28 July 2017

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1 reference

Fatcat

https://api.fatcat.wiki/v0/release/jzf76zst2zfjriferjvd3rysf4

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMC publication ID

2882389

1 reference

28 July 2017

1 reference