(Q33691356)

28 July 2017

title

Quantifying the mapping precision of genome-wide association studies using whole-genome sequencing data (English)

1 reference

genome-wide association study

28 July 2017

main subject

0 references

whole genome sequencing

1 reference

Yang Wu

1

0 references

Jian Yang

object named as

Jian Yang

series ordinal

4

0 references

Peter M. Visscher

series ordinal

3

object named as

Peter M Visscher

1 reference

28 July 2017

Zhili Zheng

2

1 reference

28 July 2017

publication date

16 May 2017

1 reference

28 July 2017

1 reference

28 July 2017

volume

18

1 reference

28 July 2017

issue

1

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28 July 2017

page(s)

86

1 reference

Deep sequencing of 10,000 human genomes

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5432979

A reference panel of 64,976 haplotypes for genotype imputation

21 June 2018

1 reference

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Systematic Functional Dissection of Common Genetic Variation Affecting Red Blood Cell Traits

21 June 2018

1 reference

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Schizophrenia risk from complex variation of complement component 4

21 June 2018

1 reference

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The (in)famous GWAS P-value threshold revisited and updated for low-frequency variants

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5432979

Partitioning heritability by functional annotation using genome-wide association summary statistics

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5432979

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5432979

The UK10K project identifies rare variants in health and disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5432979

Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5432979

FTO Obesity Variant Circuitry and Adipocyte Browning in Humans

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5432979

Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5432979

Genetic and epigenetic fine mapping of causal autoimmune disease variants

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5432979

Defining the role of common variation in the genomic and biological architecture of adult human height

21 June 2018

1 reference

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A general approach for haplotype phasing across the full spectrum of relatedness

21 June 2018

1 reference

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Cohort Profile: the Health and Retirement Study (HRS).

21 June 2018

1 reference

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Obesity-associated variants within FTO form long-range functional connections with IRX3

21 June 2018

1 reference

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The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5432979

Estimating genetic effects and quantifying missing heritability explained by identified rare-variant associations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5432979

Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP array

21 June 2018

1 reference

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GCTA: a tool for genome-wide complex trait analysis

21 June 2018

1 reference

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A map of human genome variation from population-scale sequencing

21 June 2018

1 reference

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From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5432979

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5432979

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5432979

A haplotype map of the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5432979

21 June 2018

Deeper into the genome

1 reference

Crossref

https://api.crossref.org/works/10.1186%2FS13059-017-1216-0

10.1186/S13059-017-1216-0

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

28 July 2017

0 references

1 reference

28 July 2017

1 reference