Studying copy number variations using a nanofluidic platform

Copy number variations (CNVs) in the human genome are conventionally detected using high-throughput scanning technologies, such as comparative genomic hybridization and high-density single nucleotide polymorphism (SNP) microarrays, or relatively low-throughput techniques, such as quantitative polyme...

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Detalles Bibliográficos
Autores principales: Qin, Jian, Jones, Robert C., Ramakrishnan, Ramesh
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Methods Online
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2566873/
https://www.ncbi.nlm.nih.gov/pubmed/18710881
http://dx.doi.org/10.1093/nar/gkn518

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2566873/
https://www.ncbi.nlm.nih.gov/pubmed/18710881
http://dx.doi.org/10.1093/nar/gkn518

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