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...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Christian Vogler, Leo Gschwind, Benno Röthlisberger, Andreas Huber, Isabel Filges, Peter Miny, Bianca Auschra, Attila Stetak, Philippe Demougin, Vanja Vukojevic, Iris-Tatjana Kolassa, Thomas Elbert, Dominique J-F de Quervain, Andreas Papassotiropoulos
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2010
Materias:
R
Q
Acceso en línea:https://doaj.org/article/63b360f749c14facb991fce2fafe84f9
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares