Literature DB >> 9822349

Automated recognition of patterns characteristic of subcellular structures in fluorescence microscopy images.

M V Boland1, M K Markey, R F Murphy.   

Abstract

Methods for numerical description and subsequent classification of cellular protein localization patterns are described. Images representing the localization patterns of 4 proteins and DNA were obtained using fluorescence microscopy and divided into distinct training and test sets. The images were processed to remove out-of-focus and background fluorescence and 2 sets of numeric features were generated: Zernike moments and Haralick texture features. These feature sets were used as inputs to either a classification tree or a neural network. Classifier performance (the average percent of each type of image correctly classified) on previously unseen images ranged from 63% for a classification tree using Zernike moments to 88% for a backpropagation neural network using a combination of features from the 2 feature sets. These results demonstrate the feasibility of applying pattern recognition methods to subcellular localization patterns, enabling sets of previously unseen images from a single class to be classified with an expected accuracy greater than 99%. This will provide not only a new automated way to describe proteins, based on localization rather than sequence, but also has potential application in the automation of microscope functions and in the field of gene discovery.

Mesh:

Substances:

Year:  1998        PMID: 9822349

Source DB:  PubMed          Journal:  Cytometry        ISSN: 0196-4763


  63 in total

1.  The life sciences Global Image Database (GID).

Authors:  E Gonzalez-Couto; B Hayes; A Danckaert
Journal:  Nucleic Acids Res       Date:  2001-01-01       Impact factor: 16.971

Review 2.  Chemical genetics: ligand-based discovery of gene function.

Authors:  B R Stockwell
Journal:  Nat Rev Genet       Date:  2000-11       Impact factor: 53.242

3.  Toward objective selection of representative microscope images.

Authors:  M K Markey; M V Boland; R F Murphy
Journal:  Biophys J       Date:  1999-04       Impact factor: 4.033

Review 4.  From quantitative microscopy to automated image understanding.

Authors:  Kai Huang; Robert F Murphy
Journal:  J Biomed Opt       Date:  2004 Sep-Oct       Impact factor: 3.170

5.  A quantitative analytic pipeline for evaluating neuronal activities by high-throughput synaptic vesicle imaging.

Authors:  Jing Fan; Xiaofeng Xia; Ying Li; Jennifer G Dy; Stephen T C Wong
Journal:  Neuroimage       Date:  2012-06-23       Impact factor: 6.556

Review 6.  Automated quantitative live cell fluorescence microscopy.

Authors:  Michael Fero; Kit Pogliano
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-06-30       Impact factor: 10.005

Review 7.  Automated interpretation of subcellular patterns in fluorescence microscope images for location proteomics.

Authors:  Xiang Chen; Meel Velliste; Robert F Murphy
Journal:  Cytometry A       Date:  2006-07       Impact factor: 4.355

8.  High-throughput microscopy must re-invent the microscope rather than speed up its functions.

Authors:  M Oheim
Journal:  Br J Pharmacol       Date:  2007-07-02       Impact factor: 8.739

9.  Large-scale automated analysis of location patterns in randomly tagged 3T3 cells.

Authors:  Elvira García Osuna; Juchang Hua; Nicholas W Bateman; Ting Zhao; Peter B Berget; Robert F Murphy
Journal:  Ann Biomed Eng       Date:  2007-02-07       Impact factor: 3.934

10.  IICBU 2008: a proposed benchmark suite for biological image analysis.

Authors:  Lior Shamir; Nikita Orlov; David Mark Eckley; Tomasz J Macura; Ilya G Goldberg
Journal:  Med Biol Eng Comput       Date:  2008-07-31       Impact factor: 2.602

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.