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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...
| Autores principales: | , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2009
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| Materias: | |
| 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 |