Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1471-2164

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits ; volume:17 ; number:1 ; day:13 ; month:6 ; year:2016 ; pages:1-14 ; date:12.2016
BMC genomics ; 17, Heft 1 (13.6.2016), 1-14, 12.2016

Creator: da Silva, Joaquim Manoel

Contributor: Giachetto, Poliana Fernanda
da Silva, Luiz Otávio
Cintra, Leandro Carrijo
Paiva, Samuel Rezende
Yamagishi, Michel Eduardo Beleza
Caetano, Alexandre Rodrigues
SpringerLink (Online service)

DOI: 10.1186/s12864-016-2752-9

URN: urn:nbn:de:1111-201606158830

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:52 AM CEST

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da Silva, Joaquim Manoel
Giachetto, Poliana Fernanda
da Silva, Luiz Otávio
Cintra, Leandro Carrijo
Paiva, Samuel Rezende
Yamagishi, Michel Eduardo Beleza
Caetano, Alexandre Rodrigues
SpringerLink (Online service)

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Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits

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Other Objects (12)

PennCNV in whole-genome sequencing data

Genome-wide algorithm for detecting CNV associations with diseases

Whole genome sequencing of simmental cattle for SNP and CNV discovery

Genome-wide copy number variation (CNV) in patients with autoimmune Addison's disease

X-CNV: genome-wide prediction of the pathogenicity of copy number variations

Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients

Genome-wide CNV analysis in mouse induced pluripotent stem cells reveals dosage effect of pluripotent factors on genome integrity

GenomeTornadoPlot: a novel R package for CNV visualization and focality analysis

First genome-wide CNV mapping in FELIS CATUS using next generation sequencing data

Genome-wide CNV analysis reveals variants associated with growth traits in Bos indicus

CNV discovery for milk composition traits in dairy cattle using whole genome resequencing

Genome-wide detection of CNV regions between Anqing six-end-white and Duroc pigs

PennCNV in whole-genome sequencing data

Genome-wide algorithm for detecting CNV associations with diseases

Whole genome sequencing of simmental cattle for SNP and CNV discovery

Genome-wide copy number variation (CNV) in patients with autoimmune Addison's disease

X-CNV: genome-wide prediction of the pathogenicity of copy number variations

Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients

Genome-wide CNV analysis in mouse induced pluripotent stem cells reveals dosage effect of pluripotent factors on genome integrity

GenomeTornadoPlot: a novel R package for CNV visualization and focality analysis

First genome-wide CNV mapping in FELIS CATUS using next generation sequencing data

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Genome-wide detection of CNV regions between Anqing six-end-white and Duroc pigs

PennCNV in whole-genome sequencing data

Genome-wide algorithm for detecting CNV associations with diseases

Whole genome sequencing of simmental cattle for SNP and CNV discovery

Genome-wide copy number variation (CNV) in patients with autoimmune Addison's disease

X-CNV: genome-wide prediction of the pathogenicity of copy number variations

Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients

Genome-wide CNV analysis in mouse induced pluripotent stem cells reveals dosage effect of pluripotent factors on genome integrity

GenomeTornadoPlot: a novel R package for CNV visualization and focality analysis

First genome-wide CNV mapping in FELIS CATUS using next generation sequencing data

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CNV discovery for milk composition traits in dairy cattle using whole genome resequencing

Genome-wide detection of CNV regions between Anqing six-end-white and Duroc pigs

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