Reconstructing CNV genotypes using segregation analysis: combining pedigree information with CNV assay

BACKGROUND: Repeated blocks of genome sequence have been shown to be associated with genetic diversity and disease risk in humans, and with phenotypic diversity in model organisms and domestic animals. Reliable tests are desirable to determine whether individuals are carriers of copy number variants...

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Detalles Bibliográficos
Autores principales: Henshall, John M, Whan, Vicki A, Norris, Belinda J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2928190/
https://www.ncbi.nlm.nih.gov/pubmed/20701809
http://dx.doi.org/10.1186/1297-9686-42-34

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2928190/
https://www.ncbi.nlm.nih.gov/pubmed/20701809
http://dx.doi.org/10.1186/1297-9686-42-34

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