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Copy number variation and susceptibility to complex traits
Copy number variations (CNV) within the genome are extremely abundant. In this closeup, Canales and Walz discuss how CNV are associated with normal variation, genomic disorders, genome evolution, adaptive traits and how the use of a novel screen described by Ermakova et al in this issue that is desi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401997/ https://www.ncbi.nlm.nih.gov/pubmed/21204264 http://dx.doi.org/10.1002/emmm.201000111 |
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author | Canales, Cesar P Walz, Katherina |
author_facet | Canales, Cesar P Walz, Katherina |
author_sort | Canales, Cesar P |
collection | PubMed |
description | Copy number variations (CNV) within the genome are extremely abundant. In this closeup, Canales and Walz discuss how CNV are associated with normal variation, genomic disorders, genome evolution, adaptive traits and how the use of a novel screen described by Ermakova et al in this issue that is designed to identify human disease-relevant phenotypes associated with CNV in the mouse can help elucidating susceptibility or predisposition to diseases loci. |
format | Online Article Text |
id | pubmed-3401997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | WILEY-VCH Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-34019972012-09-17 Copy number variation and susceptibility to complex traits Canales, Cesar P Walz, Katherina EMBO Mol Med Closeup Copy number variations (CNV) within the genome are extremely abundant. In this closeup, Canales and Walz discuss how CNV are associated with normal variation, genomic disorders, genome evolution, adaptive traits and how the use of a novel screen described by Ermakova et al in this issue that is designed to identify human disease-relevant phenotypes associated with CNV in the mouse can help elucidating susceptibility or predisposition to diseases loci. WILEY-VCH Verlag 2011-01 /pmc/articles/PMC3401997/ /pubmed/21204264 http://dx.doi.org/10.1002/emmm.201000111 Text en Copyright © 2011 EMBO Molecular Medicine |
spellingShingle | Closeup Canales, Cesar P Walz, Katherina Copy number variation and susceptibility to complex traits |
title | Copy number variation and susceptibility to complex traits |
title_full | Copy number variation and susceptibility to complex traits |
title_fullStr | Copy number variation and susceptibility to complex traits |
title_full_unstemmed | Copy number variation and susceptibility to complex traits |
title_short | Copy number variation and susceptibility to complex traits |
title_sort | copy number variation and susceptibility to complex traits |
topic | Closeup |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401997/ https://www.ncbi.nlm.nih.gov/pubmed/21204264 http://dx.doi.org/10.1002/emmm.201000111 |
work_keys_str_mv | AT canalescesarp copynumbervariationandsusceptibilitytocomplextraits AT walzkatherina copynumbervariationandsusceptibilitytocomplextraits |