(Q44799780)

6 December 2017

title

A genome-wide survey of copy number variations in Han Chinese residing in Taiwan (English)

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6 December 2017

5

Yuan-Tsong Chen

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6 December 2017

Chien-Hsing Lin

1

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6 December 2017

Ying-Chao Lin

2

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6 December 2017

Jer-Yuarn Wu

3

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6 December 2017

Wen-Harn Pan

4

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6 December 2017

Cathy S J Fann

6

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6 December 2017

publication date

25 June 2009

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6 December 2017

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6 December 2017

volume

94

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6 December 2017

issue

4

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6 December 2017

page(s)

241-246

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Copy number variation: new insights in genome diversity

6 December 2017

cites work

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

Detection of large-scale variation in the human genome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

Global variation in copy number in the human genome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

Large-scale copy number polymorphism in the human genome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

The fine-scale and complex architecture of human copy-number variation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

Strong association of de novo copy number mutations with autism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

Diet and the evolution of human amylase gene copy number variation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

Whole genome DNA copy number changes identified by high density oligonucleotide arrays

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPs

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

A large-scale survey of genetic copy number variations among Han Chinese residing in Taiwan

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

A census of human cancer genes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

Multiple Endocrine Neoplasia type 1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

MicroRNAs: genomics, biogenesis, mechanism, and function

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

Relative impact of nucleotide and copy number variation on gene expression phenotypes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

Han Chinese cell and genome bank in Taiwan: purpose, design and ethical considerations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

Long contiguous stretches of homozygosity in the human genome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2009.06.004

10.1016/J.YGENO.2009.06.004

7 January 2021

Identifiers

DOI

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6 December 2017

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