Single-cell gene expression profiling and cell state dynamics: collecting data, correlating data points and connecting the dots. (June 2016)
- Record Type:
- Journal Article
- Title:
- Single-cell gene expression profiling and cell state dynamics: collecting data, correlating data points and connecting the dots. (June 2016)
- Main Title:
- Single-cell gene expression profiling and cell state dynamics: collecting data, correlating data points and connecting the dots
- Authors:
- Marr, Carsten
Zhou, Joseph X
Huang, Sui - Abstract:
- Graphical abstract: Highlights: High-dimensional transcript and protein profiling at single-cell resolution. Low-dimensional longitudinal monitoring of single cells and progeny. New data stimulates development of computational tools for descriptive analysis. Linking single-cell resolution molecular profiles to underlying dynamical system. Data-driven reconstruction of the quasi-potential landscape now within reach. Abstract : Single-cell analyses of transcript and protein expression profiles — more precisely, single-cell resolution analysis of molecular profiles of cell populations — have now entered the center stage with widespread applications of single-cell qPCR, single-cell RNA-Seq and CyTOF. These high-dimensional population snapshot techniques are complemented by low-dimensional time-resolved, microscopy-based monitoring methods. Both fronts of advance have exposed a rich heterogeneity of cell states within uniform cell populations in many biological contexts, producing a new kind of data that has triggered computational analysis methods for data visualization, dimensionality reduction, and cluster (subpopulation) identification. The next step is now to go beyond collecting data and correlating data points: to connect the dots, that is, to understand what actually underlies the identified data patterns. This entails interpreting the 'clouds of points' in state space as a manifestation of the underlying molecular regulatory network. In that way control of cell stateGraphical abstract: Highlights: High-dimensional transcript and protein profiling at single-cell resolution. Low-dimensional longitudinal monitoring of single cells and progeny. New data stimulates development of computational tools for descriptive analysis. Linking single-cell resolution molecular profiles to underlying dynamical system. Data-driven reconstruction of the quasi-potential landscape now within reach. Abstract : Single-cell analyses of transcript and protein expression profiles — more precisely, single-cell resolution analysis of molecular profiles of cell populations — have now entered the center stage with widespread applications of single-cell qPCR, single-cell RNA-Seq and CyTOF. These high-dimensional population snapshot techniques are complemented by low-dimensional time-resolved, microscopy-based monitoring methods. Both fronts of advance have exposed a rich heterogeneity of cell states within uniform cell populations in many biological contexts, producing a new kind of data that has triggered computational analysis methods for data visualization, dimensionality reduction, and cluster (subpopulation) identification. The next step is now to go beyond collecting data and correlating data points: to connect the dots, that is, to understand what actually underlies the identified data patterns. This entails interpreting the 'clouds of points' in state space as a manifestation of the underlying molecular regulatory network. In that way control of cell state dynamics can be formalized as a quasi-potential landscape, as first proposed by Waddington. We summarize key methods of data acquisition and computational analysis and explain the principles that link the single-cell resolution measurements to dynamical systems theory. … (more)
- Is Part Of:
- Current opinion in biotechnology. Volume 39(2016)
- Journal:
- Current opinion in biotechnology
- Issue:
- Volume 39(2016)
- Issue Display:
- Volume 39, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 39
- Issue:
- 2016
- Issue Sort Value:
- 2016-0039-2016-0000
- Page Start:
- 207
- Page End:
- 214
- Publication Date:
- 2016-06
- Subjects:
- Biotechnology -- Periodicals
660.6 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09581669 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.copbio.2016.04.015 ↗
- Languages:
- English
- ISSNs:
- 0958-1669
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3500.772500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 9092.xml