(Q41882858)

13 October 2017

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies (English)

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genome-wide association study

13 October 2017

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13 October 2017

Bogdan Pasaniuc

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Paul Lichtenstein

object named as

Paul Lichtenstein

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Christina M. Hultman

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object named as

Christina M Hultman

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13 October 2017

9

Mark J Daly

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Noah Zaitlen

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13 October 2017

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Patrick F Sullivan

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Pamela Sklar

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13 October 2017

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Nick Patterson

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13 October 2017

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David Reich

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13 October 2017

2

Nadin Rohland

1 reference

13 October 2017

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Benjamin M Neale

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13 October 2017

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Alkes L Price

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13 October 2017

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Shaun M Purcell

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13 October 2017

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Namrata Gupta

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13 October 2017

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Paul I W de Bakker

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13 October 2017

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Shamil Sunyaev

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13 October 2017

Kiran Garimella

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13 October 2017

David W Haas

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13 October 2017

Liming Liang

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13 October 2017

language of work or name

English

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publication date

20 May 2012

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13 October 2017

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13 October 2017

44

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13 October 2017

631-635

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13 October 2017

6

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https://scigraph.springernature.com/pub.10.1038/ng.2283

13 October 2017

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cites work

Cost-effective, high-throughput DNA sequencing libraries for multiplexed target capture

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Genotype and SNP calling from next-generation sequencing data

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

A framework for variation discovery and genotyping using next-generation DNA sequencing data

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Efficient study design for next generation sequencing

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

The major genetic determinants of HIV-1 control affect HLA class I peptide presentation

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

A map of human genome variation from population-scale sequencing

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

SNP detection and genotyping from low-coverage sequencing data on multiple diploid samples

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Advances in understanding cancer genomes through second-generation sequencing

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Integrating common and rare genetic variation in diverse human populations

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Design of association studies with pooled or un-pooled next-generation sequencing data

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Genotype imputation for genome-wide association studies

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Understanding mechanisms underlying human gene expression variation with RNA sequencing

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Transcriptome genetics using second generation sequencing in a Caucasian population

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Accurate detection and genotyping of SNPs utilizing population sequencing data

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Sequencing technologies - the next generation

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Simultaneous genotype calling and haplotype phasing improves genotype accuracy and reduces false-positive associations for genome-wide association studies

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

New models of collaboration in genome-wide association studies: the Genetic Association Information Network

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Linkage disequilibrium in humans: models and data

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Genomic control for association studies

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Overlapping pools for high-throughput targeted resequencing

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3400344

Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants

18 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.2283

Tests for Linear Trends in Proportions and Frequencies

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.2283

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NG.2283

1 reference

Dimensions Publication ID

13 October 2017

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1 reference

13 October 2017

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