Mutation spectrum of Drosophila CNVs revealed by breakpoint sequencing

BACKGROUND: The detailed study of breakpoints associated with copy number variants (CNVs) can elucidate the mutational mechanisms that generate them and the comparison of breakpoints across species can highlight differences in genomic architecture that may lead to lineage-specific differences in pat...

Descripción completa

Detalles Bibliográficos
Autores principales: Cardoso-Moreira, Margarida, Arguello, J Roman, Clark, Andrew G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056370/
https://www.ncbi.nlm.nih.gov/pubmed/23259534
http://dx.doi.org/10.1186/gb-2012-13-12-r119

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056370/
https://www.ncbi.nlm.nih.gov/pubmed/23259534
http://dx.doi.org/10.1186/gb-2012-13-12-r119

Ejemplares similares