| Literature DB >> 27032065 |
Amy Reece1, Bingzhao Xia1, Zhongliang Jiang1, Benjamin Noren1, Ralph McBride1, John Oakey2.
Abstract
The microfabrication of microfluidic control systems and the development of increasingly sensitive molecular amplification tools have enabled the miniaturization of single cells analytical platforms. Only recently has the throughput of these platforms increased to a level at which populations can be screened at the single cell level. Techniques based upon both active and passive manipulation are now capable of discriminating between single cell phenotypes for sorting, diagnostic or prognostic applications in a variety of clinical scenarios. The introduction of multiphase microfluidics enables the segmentation of single cells into biochemically discrete picoliter environments. The combination of these techniques are enabling a class of single cell analytical platforms within great potential for data driven biomedicine, genomics and transcriptomics.Entities:
Mesh:
Year: 2016 PMID: 27032065 PMCID: PMC4975615 DOI: 10.1016/j.copbio.2016.02.015
Source DB: PubMed Journal: Curr Opin Biotechnol ISSN: 0958-1669 Impact factor: 9.740