High resolution discovery and confirmation of copy number variants in 90 Yoruba Nigerians (Q34964608)

5 August 2017

title

High resolution discovery and confirmation of copy number variants in 90 Yoruba Nigerians (English)

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5 August 2017

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1 reference

Hajime Matsuzaki

1

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5 August 2017

Pei-Hua Wang

2

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5 August 2017

Jing Hu

3

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5 August 2017

Rich Rava

4

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5 August 2017

Glenn K Fu

5

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5 August 2017

publication date

9 November 2009

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5 August 2017

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5 August 2017

volume

10

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5 August 2017

issue

11

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5 August 2017

page(s)

R125

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The diploid genome sequence of an Asian individual

5 August 2017

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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Paired-end mapping reveals extensive structural variation in the human genome

8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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Mutational and selective effects on copy-number variants in the human genome

8 July 2018

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8 July 2018

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Strong association of de novo copy number mutations with autism

8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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

8 July 2018

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8 July 2018

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Structural variation in the human genome

8 July 2018

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8 July 2018

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A haplotype map of the human genome

8 July 2018

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8 July 2018

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Fine-scale structural variation of the human genome

8 July 2018

1 reference

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Detection of large-scale variation in the human genome

8 July 2018

1 reference

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Large-scale copy number polymorphism in the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091319

A comparison of normalization methods for high density oligonucleotide array data based on variance and bias

8 July 2018

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8 July 2018

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8 July 2018

1 reference

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8 July 2018

1 reference

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Light-directed, spatially addressable parallel chemical synthesis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091319

Common deletion polymorphisms in the human genome.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091319

Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091319

Common deletions and SNPs are in linkage disequilibrium in the human genome

9 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3091319

A high-resolution survey of deletion polymorphism in the human genome

9 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19900272

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/GB-2009-10-11-R125

1 reference

Dimensions Publication ID

5 August 2017

0 references

1 reference

5 August 2017

1 reference