Abstract

Background

Studies of cell-to-cell variation have in recent years grown in interest, due to improved bioanalytical techniques which facilitates determination of small changes with high uncertainty. Like much high-quality data, single-cell data is best analysed using a systems biology approach. The most common systems biology approach to single-cell data is the standard two-stage (STS) approach. In STS, data from each cell is analysed in a separate sub-problem, meaning that only data from the same cell is used to calculate the parameter values within that cell. Because only parts of the data are considered, problems with parameter unidentifiability are exaggerated in STS. In contrast, a related approach to data analysis has been developed for the studies of patient-to-patient variations. This approach, called nonlinear mixed-effects modelling (NLME), makes use of all data, when estimating the patient-specific parameters. NLME would therefore be advantageous compared to STS also for the study of cell-to-cell variation. However, no such systematic evaluation of the two approaches exists.

Results

Herein, such a systematic comparison between STS and NLME has been performed. Different examples, both linear and nonlinear, and both simulated and real experimental data, have been examined. With informative data, there is no significant difference in the results for either parameter or noise estimation. However, when data becomes uninformative, NLME is significantly superior to STS. These results hold independently of whether the loss of information is due to a low signal-to-noise ratio, too few data points, or a bad input signal. The improvement is shown to come from both the consideration of a joint likelihood (JLH) function, describing all parameters and data, and from an a priori postulated form of the population parameters. Finally, we provide a small tutorial that shows how to use NLME for single-cell analysis, using the free and user-friendly software Monolix.

Conclusions

When considering uninformative single-cell data, NLME yields more accurate parameter and noise estimates, compared to more traditional approaches, such as STS and JLH.

Details

Title
Nonlinear mixed-effects modelling for single cell estimation: when, why, and how to use it
Author
Karlsson, Markus; David LI Janzen; Durrieu, Lucia; Colman-Lerner, Alejandro; Kjellsson, Maria C; Cedersund, Gunnar
Publication year
2015
Publication date
2015
Publisher
BioMed Central
e-ISSN
1752-0509
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1780025851
Copyright
Copyright BioMed Central 2015