Quadruplex MAPH: improvement of throughput in high-resolution copy number screening

BACKGROUND: Copy number variation (CNV) in the human genome is recognised as a widespread and important source of human genetic variation. Now the challenge is to screen for these CNVs at high resolution in a reliable, accurate and cost-effective way. RESULTS: Multiplex Amplifiable Probe Hybridisati...

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Detalles Bibliográficos
Autores principales: Tyson, Jess, Majerus, Tamsin MO, Walker, Susan, Armour, John AL
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2761424/
https://www.ncbi.nlm.nih.gov/pubmed/19785739
http://dx.doi.org/10.1186/1471-2164-10-453

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2761424/
https://www.ncbi.nlm.nih.gov/pubmed/19785739
http://dx.doi.org/10.1186/1471-2164-10-453

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