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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...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2010
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| Materias: | |
| 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 |