Cargando…

Context based mixture model for cell phase identification in automated fluorescence microscopy

BACKGROUND: Automated identification of cell cycle phases of individual live cells in a large population captured via automated fluorescence microscopy technique is important for cancer drug discovery and cell cycle studies. Time-lapse fluorescence microscopy images provide an important method to st...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Meng, Zhou, Xiaobo, King, Randy W, Wong, Stephen TC
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1800869/
https://www.ncbi.nlm.nih.gov/pubmed/17263881
http://dx.doi.org/10.1186/1471-2105-8-32
_version_ 1782132356229890048
author Wang, Meng
Zhou, Xiaobo
King, Randy W
Wong, Stephen TC
author_facet Wang, Meng
Zhou, Xiaobo
King, Randy W
Wong, Stephen TC
author_sort Wang, Meng
collection PubMed
description BACKGROUND: Automated identification of cell cycle phases of individual live cells in a large population captured via automated fluorescence microscopy technique is important for cancer drug discovery and cell cycle studies. Time-lapse fluorescence microscopy images provide an important method to study the cell cycle process under different conditions of perturbation. Existing methods are limited in dealing with such time-lapse data sets while manual analysis is not feasible. This paper presents statistical data analysis and statistical pattern recognition to perform this task. RESULTS: The data is generated from Hela H2B GFP cells imaged during a 2-day period with images acquired 15 minutes apart using an automated time-lapse fluorescence microscopy. The patterns are described with four kinds of features, including twelve general features, Haralick texture features, Zernike moment features, and wavelet features. To generate a new set of features with more discriminate power, the commonly used feature reduction techniques are used, which include Principle Component Analysis (PCA), Linear Discriminant Analysis (LDA), Maximum Margin Criterion (MMC), Stepwise Discriminate Analysis based Feature Selection (SDAFS), and Genetic Algorithm based Feature Selection (GAFS). Then, we propose a Context Based Mixture Model (CBMM) for dealing with the time-series cell sequence information and compare it to other traditional classifiers: Support Vector Machine (SVM), Neural Network (NN), and K-Nearest Neighbor (KNN). Being a standard practice in machine learning, we systematically compare the performance of a number of common feature reduction techniques and classifiers to select an optimal combination of a feature reduction technique and a classifier. A cellular database containing 100 manually labelled subsequence is built for evaluating the performance of the classifiers. The generalization error is estimated using the cross validation technique. The experimental results show that CBMM outperforms all other classifies in identifying prophase and has the best overall performance. CONCLUSION: The application of feature reduction techniques can improve the prediction accuracy significantly. CBMM can effectively utilize the contextual information and has the best overall performance when combined with any of the previously mentioned feature reduction techniques.
format Text
id pubmed-1800869
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-18008692007-02-23 Context based mixture model for cell phase identification in automated fluorescence microscopy Wang, Meng Zhou, Xiaobo King, Randy W Wong, Stephen TC BMC Bioinformatics Research Article BACKGROUND: Automated identification of cell cycle phases of individual live cells in a large population captured via automated fluorescence microscopy technique is important for cancer drug discovery and cell cycle studies. Time-lapse fluorescence microscopy images provide an important method to study the cell cycle process under different conditions of perturbation. Existing methods are limited in dealing with such time-lapse data sets while manual analysis is not feasible. This paper presents statistical data analysis and statistical pattern recognition to perform this task. RESULTS: The data is generated from Hela H2B GFP cells imaged during a 2-day period with images acquired 15 minutes apart using an automated time-lapse fluorescence microscopy. The patterns are described with four kinds of features, including twelve general features, Haralick texture features, Zernike moment features, and wavelet features. To generate a new set of features with more discriminate power, the commonly used feature reduction techniques are used, which include Principle Component Analysis (PCA), Linear Discriminant Analysis (LDA), Maximum Margin Criterion (MMC), Stepwise Discriminate Analysis based Feature Selection (SDAFS), and Genetic Algorithm based Feature Selection (GAFS). Then, we propose a Context Based Mixture Model (CBMM) for dealing with the time-series cell sequence information and compare it to other traditional classifiers: Support Vector Machine (SVM), Neural Network (NN), and K-Nearest Neighbor (KNN). Being a standard practice in machine learning, we systematically compare the performance of a number of common feature reduction techniques and classifiers to select an optimal combination of a feature reduction technique and a classifier. A cellular database containing 100 manually labelled subsequence is built for evaluating the performance of the classifiers. The generalization error is estimated using the cross validation technique. The experimental results show that CBMM outperforms all other classifies in identifying prophase and has the best overall performance. CONCLUSION: The application of feature reduction techniques can improve the prediction accuracy significantly. CBMM can effectively utilize the contextual information and has the best overall performance when combined with any of the previously mentioned feature reduction techniques. BioMed Central 2007-01-30 /pmc/articles/PMC1800869/ /pubmed/17263881 http://dx.doi.org/10.1186/1471-2105-8-32 Text en Copyright © 2007 Wang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Meng
Zhou, Xiaobo
King, Randy W
Wong, Stephen TC
Context based mixture model for cell phase identification in automated fluorescence microscopy
title Context based mixture model for cell phase identification in automated fluorescence microscopy
title_full Context based mixture model for cell phase identification in automated fluorescence microscopy
title_fullStr Context based mixture model for cell phase identification in automated fluorescence microscopy
title_full_unstemmed Context based mixture model for cell phase identification in automated fluorescence microscopy
title_short Context based mixture model for cell phase identification in automated fluorescence microscopy
title_sort context based mixture model for cell phase identification in automated fluorescence microscopy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1800869/
https://www.ncbi.nlm.nih.gov/pubmed/17263881
http://dx.doi.org/10.1186/1471-2105-8-32
work_keys_str_mv AT wangmeng contextbasedmixturemodelforcellphaseidentificationinautomatedfluorescencemicroscopy
AT zhouxiaobo contextbasedmixturemodelforcellphaseidentificationinautomatedfluorescencemicroscopy
AT kingrandyw contextbasedmixturemodelforcellphaseidentificationinautomatedfluorescencemicroscopy
AT wongstephentc contextbasedmixturemodelforcellphaseidentificationinautomatedfluorescencemicroscopy