共 101 条
Finding a helix in a haystack: nucleic acid cytometry with droplet microfluidics
被引:24
作者:

Clark, Iain C.
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机构:
Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA

Abate, Adam R.
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h-index: 0
机构:
Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
机构:
[1] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
关键词:
POLYMERASE-CHAIN-REACTION;
PARALLEL SINGLE-MOLECULE;
DOUBLE EMULSION DROPLETS;
NONCODING RNAS;
TRANSCRIPTIONAL SIGNATURES;
DIRECTED EVOLUTION;
NANOLITER DROPLETS;
FLOW-CYTOMETRY;
CELL ANALYSIS;
CANCER;
D O I:
10.1039/c7lc00241f
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Nucleic acids encode the information of life, programming cellular functions and dictating many biological outcomes. Differentiating between cells based on their nucleic acid programs is, thus, a powerful way to unravel the genetic bases of many phenotypes. This is especially important considering that most cells exist in heterogeneous populations, requiring them to be isolated before they can be studied. Existing flow cytometry techniques, however, are unable to reliably recover specific cells based on nucleic acid content. Nucleic acid cytometry is a new field built on droplet microfluidics that allows robust identification, sorting, and sequencing of cells based on specific nucleic acid biomarkers. This review highlights applications that immediately benefit from the approach, biological questions that can be addressed for the first time with it, and considerations for building successful workflows.
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页码:2032 / 2045
页数:14
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