Microarray-Based Maps of Copy-Number Variant Regions in European and Sub-Saharan Populations

The genetic basis of phenotypic variation can be partially explained by the presence of copy-number variations (CNVs). Currently available methods for CNV assessment include high-density single-nucleotide polymorphism (SNP) microarrays that have become an indispensable tool in genome-wide associatio...

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Detalles Bibliográficos
Autores principales: Vogler, Christian, Gschwind, Leo, Röthlisberger, Benno, Huber, Andreas, Filges, Isabel, Miny, Peter, Auschra, Bianca, Stetak, Attila, Demougin, Philippe, Vukojevic, Vanja, Kolassa, Iris-Tatjana, Elbert, Thomas, de Quervain, Dominique J.-F., Papassotiropoulos, Andreas
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002949/
https://www.ncbi.nlm.nih.gov/pubmed/21179565
http://dx.doi.org/10.1371/journal.pone.0015246

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002949/
https://www.ncbi.nlm.nih.gov/pubmed/21179565
http://dx.doi.org/10.1371/journal.pone.0015246

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