A genome-wide association study of copy number variations with umbilical hernia in swine.

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Genome-wide association study reveals a QTL and strong candidate genes for umbilical hernia in pigs on SSC14.

P2860

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P2860

A genome-wide association study of copy number variations with umbilical hernia in swine.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

@wuu

2016年学术文章

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2016年学术文章

@zh-cn

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@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

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@yue

2016年學術文章

@zh-hant

name

A genome-wide association study of copy number variations with umbilical hernia in swine.

@en

A genome-wide association study of copy number variations with umbilical hernia in swine.

@nl

type

Item

label

A genome-wide association study of copy number variations with umbilical hernia in swine.

@en

A genome-wide association study of copy number variations with umbilical hernia in swine.

@nl

prefLabel

A genome-wide association study of copy number variations with umbilical hernia in swine.

@en

A genome-wide association study of copy number variations with umbilical hernia in swine.

@nl

P1476

A genome-wide association study of copy number variations with umbilical hernia in swine.

@en

P2093

Bin Yang

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Guorong Ruan

http://www.w3.org/2001/XMLSchema#string

Huashui Ai

http://www.w3.org/2001/XMLSchema#string

Jun Ren

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Lusheng Huang

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Nengshui Ding

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Shijun Xiao

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Xinjun Liao

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Yi Long

http://www.w3.org/2001/XMLSchema#string

Ying Su

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P2860

Evolutionary dynamics of copy number variation in pig genomes in the context of adaptation and domestication

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

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Strong association of de novo copy number mutations with autism

Large recurrent microdeletions associated with schizophrenia

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

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

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

P304

298-305

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P31

scholarly article

P356

10.1111/AGE.12402

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P478

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2016-03-30T00:00:00Z

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27028052

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P921

genome-wide association study

A genome-wide association study of copy number variations with umbilical hernia in swine.

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P2860

P2860

A genome-wide association study of copy number variations with umbilical hernia in swine.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921