(Q34523823)

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A comprehensive survey of copy number variation in 18 diverse pig populations and identification of candidate copy number variable genes associated with complex traits

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Europe PubMed Central

PubMed publication ID

2 August 2017

A comprehensive survey of copy number variation in 18 diverse pig populations and identification of candidate copy number variable genes associated with complex traits (English)

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Europe PubMed Central

PubMed publication ID

2 August 2017

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Congying Chen

1

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Europe PubMed Central

PubMed publication ID

2 August 2017

Ruimin Qiao

2

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Europe PubMed Central

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2 August 2017

Rongxing Wei

3

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Europe PubMed Central

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2 August 2017

Yuanmei Guo

4

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Europe PubMed Central

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2 August 2017

Huashui Ai

5

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Europe PubMed Central

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2 August 2017

Junwu Ma

6

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Europe PubMed Central

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2 August 2017

Jun Ren

7

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2 August 2017

Lusheng Huang

8

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2 August 2017

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publication date

27 December 2012

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Europe PubMed Central

PubMed publication ID

2 August 2017

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Europe PubMed Central

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2 August 2017

13

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Europe PubMed Central

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2 August 2017

733

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Europe PubMed Central

PubMed publication ID

2 August 2017

https://scigraph.springernature.com/pub.10.1186/1471-2164-13-733

0 references

Identification of copy number variants in horses.

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Copy number variation across European populations

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Acidic nuclear phosphoprotein 32kDa (ANP32)B-deficient mouse reveals a hierarchy of ANP32 importance in mammalian development

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7 July 2018

Genomic characteristics of cattle copy number variations.

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7 July 2018

A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci

1 reference

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7 July 2018

Assessment of copy number variation using the Illumina Infinium 1M SNP-array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study

1 reference

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Allosteric regulation of glycogen synthase controls glycogen synthesis in muscle

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Copy number variation in the porcine genome inferred from a 60 k SNP BeadChip

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APOE/C1/C4/C2 gene cluster genotypes, haplotypes and lipid levels in prospective coronary heart disease risk among UK healthy men

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7 July 2018

CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics

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7 July 2018

Structural variation in the human genome and its role in disease

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7 July 2018

Origins and functional impact of copy number variation in the human genome

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The role of DNA copy number variation in schizophrenia.

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7 July 2018

Comparing CNV detection methods for SNP arrays

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7 July 2018

Design of a high density SNP genotyping assay in the pig using SNPs identified and characterized by next generation sequencing technology

1 reference

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Copy number variation in intron 1 of SOX5 causes the Pea-comb phenotype in chickens

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SOAP2: an improved ultrafast tool for short read alignment

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Positive Darwinian selection and the birth of an olfactory receptor clade in teleosts

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Genome-wide association study suggested copy number variation may be associated with body mass index in the Chinese population

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Copy number variation in the human genome and its implication in autoimmunity

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Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

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The genomic architecture of segmental duplications and associated copy number variants in dogs

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7 July 2018

A snapshot of CNVs in the pig genome

1 reference

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7 July 2018

Deficiency of growth differentiation factor 3 protects against diet-induced obesity by selectively acting on white adipose.

1 reference

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7 July 2018

Quantitative trait loci for porcine baseline erythroid traits at three growth ages in a White Duroc x Erhualian F(2) resource population

1 reference

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7 July 2018

A genome-wide scan for quantitative trait loci affecting limb bone lengths and areal bone mineral density of the distal femur in a White Duroc x Erhualian F2 population

1 reference

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7 July 2018

Extensive copy-number variation of the human olfactory receptor gene family

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A cis-acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse

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

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Duplication of FGF3, FGF4, FGF19 and ORAOV1 causes hair ridge and predisposition to dermoid sinus in Ridgeback dogs

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

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

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7 July 2018

Global variation in copy number in the human genome

1 reference

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21 January 2018

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1 reference

https://pubmed.ncbi.nlm.nih.gov/23270433

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1 reference

https://pubmed.ncbi.nlm.nih.gov/23270433

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Polymorphism at the porcine Dominant white/KIT locus influence coat colour and peripheral blood cell measures

1 reference

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1 reference

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Identifiers

10.1186/1471-2164-13-733

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

ResearchGate publication ID

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