Genotype, haplotype and copy-number variation in worldwide human populations (Q29615885)

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3 January 2020

title

Genotype, haplotype and copy-number variation in worldwide human populations (English)

2 references

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30 April 2017

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3 January 2020

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3 January 2020

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Jenna Vanliere Canzoniero

3 January 2020

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Bryan Traynor

object named as

Bryan J Traynor

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Dena G Hernandez

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James H Degnan

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Paul Scheet

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J Raphael Gibbs

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Jenna M VanLiere

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Hon-Chung Fung

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Zachary A Szpiech

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Kai Wang

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Rita Guerreiro

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Jose M Bras

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Jennifer C Schymick

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Mar Matarin

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Angela Britton

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Ian Rafferty

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Maja Bucan

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Howard M Cann

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John A Hardy

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Andrew B Singleton

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language of work or name

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30 April 2017

publication date

1 February 2008

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3 January 2020

number of pages

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inferred from page(s)

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30 April 2017

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3 January 2020

volume

451

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issue

7181

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3 January 2020

page(s)

998-1003

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30 April 2017

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A haplotype map of the human genome

3 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

Whole-genome patterns of common DNA variation in three human populations

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

Global variation in copy number in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

A human genome diversity cell line panel

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

The genetic structure of human populations studied through short insertion-deletion polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

Clines, clusters, and the effect of study design on the inference of human population structure

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

Genetic structure of human populations

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

Going the distance: human population genetics in a clinal world.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

Support from the relationship of genetic and geographic distance in human populations for a serial founder effect originating in Africa

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

The structure of haplotype blocks in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

Linkage disequilibrium in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

Implications of biogeography of human populations for 'race' and medicine

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

Genetic signatures of strong recent positive selection at the lactase gene

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

Convergent adaptation of human lactase persistence in Africa and Europe

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

A comprehensive analysis of common copy-number variations in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

Segmental duplications and copy-number variation in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

Challenges and standards in integrating surveys of structural variation

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

Genome-wide tagging for everyone

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

Allele frequency matching between SNPs reveals an excess of linkage disequilibrium in genic regions of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

CLUMPP: a cluster matching and permutation program for dealing with label switching and multimodality in analysis of population structure

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE06742

7 January 2021

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=18288195

Identifiers

3 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017

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Dimensions Publication ID

3 January 2020

1037825612

0 references

1 reference

Consolidated OpenCitations Corpus – April 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=18288195

3 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017

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