(Q34658885)

3 August 2017

title

Analysis of copy number variations in the sheep genome using 50K SNP BeadChip array (English)

1 reference

3 August 2017

Jiasen Liu

1

1 reference

3 August 2017

Li Zhang

2

1 reference

3 August 2017

Lingyang Xu

3

1 reference

3 August 2017

Hangxing Ren

4

1 reference

3 August 2017

Jian Lu

5

1 reference

3 August 2017

Xiaoning Zhang

6

1 reference

3 August 2017

Shifang Zhang

7

1 reference

3 August 2017

Xinlei Zhou

8

1 reference

3 August 2017

Caihong Wei

9

1 reference

3 August 2017

Fuping Zhao

10

1 reference

3 August 2017

Lixin Du

11

1 reference

3 August 2017

language of work or name

English

0 references

publication date

8 April 2013

1 reference

3 August 2017

1 reference

3 August 2017

volume

14

1 reference

3 August 2017

page(s)

229

1 reference

Exploring copy number variation in the rabbit (Oryctolagus cuniculus) genome by array comparative genome hybridization

3 August 2017

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7 July 2018

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Copy number variants in pharmacogenetic genes

7 July 2018

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7 July 2018

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7 July 2018

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An initial comparative map of copy number variations in the goat (Capra hircus) genome

7 July 2018

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

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Identification of copy number variations and common deletion polymorphisms in cattle

7 July 2018

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7 July 2018

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Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays

7 July 2018

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Copy number variation in the genomes of twelve natural isolates of Caenorhabditis elegans

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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

7 July 2018

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Copy number variation in human health, disease, and evolution

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

The HapMap and genome-wide association studies in diagnosis and therapy

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

Genomic copy number variation, human health, and disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

The genome sequence of taurine cattle: a window to ruminant biology and evolution

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

Duplications involving a conserved regulatory element downstream of BMP2 are associated with brachydactyly type A2.

7 July 2018

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A snapshot of CNVs in the pig genome

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

The evolution of animal chemosensory receptor gene repertoires: roles of chance and necessity

7 July 2018

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Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms

7 July 2018

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Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

7 July 2018

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Integrated detection and population-genetic analysis of SNPs and copy number variation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

Copy number variation and evolution in humans and chimpanzees

7 July 2018

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Mouse segmental duplication and copy number variation

7 July 2018

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

7 July 2018

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Sparse representation and Bayesian detection of genome copy number alterations from microarray data

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

A high utility integrated map of the pig genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

A high-resolution map of segmental DNA copy number variation in the mouse genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

Global variation in copy number in the human genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

Copy number variation: new insights in genome diversity

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

Hotspots for copy number variation in chimpanzees and humans

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

Structural variation in the human genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

Determination of cytochrome P450 2D6 (CYP2D6) gene copy number by real-time quantitative PCR.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

Detection of large-scale variation in the human genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

Initial sequencing and analysis of the human genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

The Sequence of the Human Genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

A first comparative map of copy number variations in the sheep genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

A specific mutation in the distant sonic hedgehog (SHH) cis-regulator (ZRS) causes Werner mesomelic syndrome (WMS) while complete ZRS duplications underlie Haas type polysyndactyly and preaxial polydactyly (PPD) with or without triphalangeal thumb

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

Duplications of noncoding elements 5' of SOX9 are associated with brachydactyly-anonychia.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

Natural selection shapes genome-wide patterns of copy-number polymorphism in Drosophila melanogaster.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studies

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3626776

Copy number variation and human genome maps

9 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23565757

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23565757

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Analysis of copy number variants in the cattle genome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23565757

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2164-14-229

1 reference

3 August 2017

1 reference

3 August 2017

1 reference