Cell segmentation by multi-resolution analysis and maximum likelihood estimation (MAMLE)

被引:20
作者
Chowdhury, Sharif [1 ]
Kandhavelu, Meenakshisundaram [1 ]
Yli-Harja, Olli [1 ,2 ]
Ribeiro, Andre S. [1 ]
机构
[1] Tampere Univ Technol, Dept Signal Proc, Computat Syst Biol Res Grp, Lab Biosyst Dynam, FIN-33101 Tampere, Finland
[2] Inst Syst Biol, Seattle, WA 98109 USA
基金
芬兰科学院;
关键词
ESCHERICHIA-COLI; KINETICS;
D O I
10.1186/1471-2105-14-S10-S8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Cell imaging is becoming an indispensable tool for cell and molecular biology research. However, most processes studied are stochastic in nature, and require the observation of many cells and events. Ideally, extraction of information from these images ought to rely on automatic methods. Here, we propose a novel segmentation method, MAMLE, for detecting cells within dense clusters. Methods: MAMLE executes cell segmentation in two stages. The first relies on state of the art filtering technique, edge detection in multi-resolution with morphological operator and threshold decomposition for adaptive thresholding. From this result, a correction procedure is applied that exploits maximum likelihood estimate as an objective function. Also, it acquires morphological features from the initial segmentation for constructing the likelihood parameter, after which the final segmentation is obtained. Conclusions: We performed an empirical evaluation that includes sample images from different imaging modalities and diverse cell types. The new method attained very high (above 90%) cell segmentation accuracy in all cases. Finally, its accuracy was compared to several existing methods, and in all tests, MAMLE outperformed them in segmentation accuracy.
引用
收藏
页数:13
相关论文
共 27 条
[1]   Improved Automatic Detection and Segmentation of Cell Nuclei in Histopathology Images [J].
Al-Kofahi, Yousef ;
Lassoued, Wiem ;
Lee, William ;
Roysam, Badrinath .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 2010, 57 (04) :841-852
[2]  
[Anonymous], 2000, Pattern Classification
[3]   Global analysis of mRNA decay and abundance in Escherichia coli at single-gene resolution using two-color fluorescent DNA microarrays [J].
Bernstein, JA ;
Khodursky, AB ;
Lin, PH ;
Lin-Chao, S ;
Cohen, SN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (15) :9697-9702
[5]   CellProfiler: image analysis software for identifying and quantifying cell phenotypes [J].
Carpenter, Anne E. ;
Jones, Thouis Ray ;
Lamprecht, Michael R. ;
Clarke, Colin ;
Kang, In Han ;
Friman, Ola ;
Guertin, David A. ;
Chang, Joo Han ;
Lindquist, Robert A. ;
Moffat, Jason ;
Golland, Polina ;
Sabatini, David M. .
GENOME BIOLOGY, 2006, 7 (10)
[6]   Image denoising by sparse 3-D transform-domain collaborative filtering [J].
Dabov, Kostadin ;
Foi, Alessandro ;
Katkovnik, Vladimir ;
Egiazarian, Karen .
IEEE TRANSACTIONS ON IMAGE PROCESSING, 2007, 16 (08) :2080-2095
[7]   A synthetic oscillatory network of transcriptional regulators [J].
Elowitz, MB ;
Leibler, S .
NATURE, 2000, 403 (6767) :335-338
[8]   Real-time kinetics of gene activity in individual bacteria [J].
Golding, I ;
Paulsson, J ;
Zawilski, SM ;
Cox, EC .
CELL, 2005, 123 (06) :1025-1036
[9]  
Hillier F. S., 2001, Introduction to Operations Research
[10]   In vivo kinetics of transcription initiation of the lar promoter in Escherichia coli. Evidence for a sequential mechanism with two rate-limiting steps [J].
Kandhavelu, Meenakshisundaram ;
Mannerstrom, Henrik ;
Gupta, Abhishekh ;
Hakkinen, Antti ;
Lloyd-Price, Jason ;
Yli-Harja, Olli ;
Ribeiro, Andre S. .
BMC SYSTEMS BIOLOGY, 2011, 5