Single cell proteomics in biomedicine: High-dimensional data acquisition, visualization, and analysis

被引:66
|
作者
Su, Yapeng [1 ]
Shi, Qihui [2 ]
Wei, Wei [1 ,3 ]
机构
[1] CALTECH, NanoSyst Biol Canc Ctr, Div Chem & Chem Engn, Pasadena, CA USA
[2] Shanghai Jiao Tong Univ, Sch Biomed Engn, Key Lab Syst Biomed Minist Educ, Shanghai, Peoples R China
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Mol & Med Pharmacol, Los Angeles, CA USA
关键词
Information theoretical approaches; Mass cytometry; Single cell barcode chip; Single cell data analysis; Single cell proteomics; STOCHASTIC GENE-EXPRESSION; FLOW-CYTOMETRY; FUNCTIONAL PROTEOMICS; MASS CYTOMETRY; PROTEIN EXPRESSION; PHASE-TRANSITION; INFORMATION; HETEROGENEITY; DYNAMICS; PROGRESSION;
D O I
10.1002/pmic.201600267
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
New insights on cellular heterogeneity in the last decade provoke the development of a variety of single cell omics tools at a lightning pace. The resultant high-dimensional single cell data generated by these tools require new theoretical approaches and analytical algorithms for effective visualization and interpretation. In this review, we briefly survey the state-of-the-art single cell proteomic tools with a particular focus on data acquisition and quantification, followed by an elaboration of a number of statistical and computational approaches developed to date for dissecting the high-dimensional single cell data. The underlying assumptions, unique features, and limitations of the analytical methods with the designated biological questions they seek to answer will be discussed. Particular attention will be given to those information theoretical approaches that are anchored in a set of first principles of physics and can yield detailed (and often surprising) predictions.
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页数:16
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