(Q35013642)

5 August 2017

title

Performance of genotype imputation for low frequency and rare variants from the 1000 genomes (English)

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5 August 2017

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Hou-Feng Zheng

1

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5 August 2017

Jing-Jing Rong

2

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5 August 2017

Ming Liu

3

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5 August 2017

Fang Han

4

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5 August 2017

Xing-Wei Zhang

5

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5 August 2017

J Brent Richards

6

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5 August 2017

Li Wang

7

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5 August 2017

language of work or name

English

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publication date

26 January 2015

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5 August 2017

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5 August 2017

volume

10

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5 August 2017

issue

1

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5 August 2017

page(s)

e0116487

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Creative Commons Attribution 4.0 International

5 August 2017

copyright license

start time

26 January 2015

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April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Empirical power of very rare variants for common traits and disease: results from sanger sequencing 1998 individuals

8 July 2018

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8 July 2018

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

8 July 2018

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

8 July 2018

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Genotype imputation with thousands of genomes

8 July 2018

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The empirical power of rare variant association methods: results from sanger sequencing in 1,998 individuals

8 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306552

Performance of genotype imputations using data from the 1000 Genomes Project

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306552

Performance of genotype imputation for rare variants identified in exons and flanking regions of genes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306552

Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction

8 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306552

Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets

8 July 2018

1 reference

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

8 July 2018

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8 July 2018

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Genotype imputation for genome-wide association studies

8 July 2018

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Missing heritability and strategies for finding the underlying causes of complex disease

8 July 2018

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Rare variants create synthetic genome-wide associations

8 July 2018

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Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture

8 July 2018

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

8 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306552

Genotype-imputation accuracy across worldwide human populations

8 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306552

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

8 July 2018

1 reference

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Personal genomes: The case of the missing heritability

8 July 2018

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Analyses and comparison of accuracy of different genotype imputation methods

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306552

Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.

8 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306552

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4306552

Are twins and singletons comparable? A study of disease-related and lifestyle characteristics in adult women

8 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0116487

Effect of genome-wide genotyping and reference panels on rare variants imputation

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25621886

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0116487

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5 August 2017

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5 August 2017

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