A method for improved clustering and classification of microscopy images using quantitative co-localization coefficients

<p>Abstract</p> <p>Background</p> <p>The localization of proteins to specific subcellular structures in eukaryotic cells provides important information with respect to their function. Fluorescence microscopy approaches to determine localization distribution have proved...

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Main Authors: Singan Vasanth R, Handzic Kenan, Curran Kathleen M, Simpson Jeremy C
Format: Article
Language:English
Published: BMC 2012-06-01
Series:BMC Research Notes
Subjects:
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spelling doaj-64ca63b34d264df1991d86dc5f6ba6472020-11-25T01:44:34ZengBMCBMC Research Notes1756-05002012-06-015128110.1186/1756-0500-5-281A method for improved clustering and classification of microscopy images using quantitative co-localization coefficientsSingan Vasanth RHandzic KenanCurran Kathleen MSimpson Jeremy C<p>Abstract</p> <p>Background</p> <p>The localization of proteins to specific subcellular structures in eukaryotic cells provides important information with respect to their function. Fluorescence microscopy approaches to determine localization distribution have proved to be an essential tool in the characterization of unknown proteins, and are now particularly pertinent as a result of the wide availability of fluorescently-tagged constructs and antibodies. However, there are currently very few image analysis options able to effectively discriminate proteins with apparently similar distributions in cells, despite this information being important for protein characterization.</p> <p>Findings</p> <p>We have developed a novel method for combining two existing image analysis approaches, which results in highly efficient and accurate discrimination of proteins with seemingly similar distributions. We have combined image texture-based analysis with quantitative co-localization coefficients, a method that has traditionally only been used to study the spatial overlap between two populations of molecules. Here we describe and present a novel application for quantitative co-localization, as applied to the study of Rab family small GTP binding proteins localizing to the endomembrane system of cultured cells.</p> <p>Conclusions</p> <p>We show how quantitative co-localization can be used alongside texture feature analysis, resulting in improved clustering of microscopy images. The use of co-localization as an additional clustering parameter is non-biased and highly applicable to high-throughput image data sets.</p> Quantitative co-localizationImage analysisTexture featuresClusteringRab proteins
collection DOAJ
language English
format Article
sources DOAJ
author Singan Vasanth R
Handzic Kenan
Curran Kathleen M
Simpson Jeremy C
spellingShingle Singan Vasanth R
Handzic Kenan
Curran Kathleen M
Simpson Jeremy C
A method for improved clustering and classification of microscopy images using quantitative co-localization coefficients
BMC Research Notes
Quantitative co-localization
Image analysis
Texture features
Clustering
Rab proteins
author_facet Singan Vasanth R
Handzic Kenan
Curran Kathleen M
Simpson Jeremy C
author_sort Singan Vasanth R
title A method for improved clustering and classification of microscopy images using quantitative co-localization coefficients
title_short A method for improved clustering and classification of microscopy images using quantitative co-localization coefficients
title_full A method for improved clustering and classification of microscopy images using quantitative co-localization coefficients
title_fullStr A method for improved clustering and classification of microscopy images using quantitative co-localization coefficients
title_full_unstemmed A method for improved clustering and classification of microscopy images using quantitative co-localization coefficients
title_sort method for improved clustering and classification of microscopy images using quantitative co-localization coefficients
publisher BMC
series BMC Research Notes
issn 1756-0500
publishDate 2012-06-01
description <p>Abstract</p> <p>Background</p> <p>The localization of proteins to specific subcellular structures in eukaryotic cells provides important information with respect to their function. Fluorescence microscopy approaches to determine localization distribution have proved to be an essential tool in the characterization of unknown proteins, and are now particularly pertinent as a result of the wide availability of fluorescently-tagged constructs and antibodies. However, there are currently very few image analysis options able to effectively discriminate proteins with apparently similar distributions in cells, despite this information being important for protein characterization.</p> <p>Findings</p> <p>We have developed a novel method for combining two existing image analysis approaches, which results in highly efficient and accurate discrimination of proteins with seemingly similar distributions. We have combined image texture-based analysis with quantitative co-localization coefficients, a method that has traditionally only been used to study the spatial overlap between two populations of molecules. Here we describe and present a novel application for quantitative co-localization, as applied to the study of Rab family small GTP binding proteins localizing to the endomembrane system of cultured cells.</p> <p>Conclusions</p> <p>We show how quantitative co-localization can be used alongside texture feature analysis, resulting in improved clustering of microscopy images. The use of co-localization as an additional clustering parameter is non-biased and highly applicable to high-throughput image data sets.</p>
topic Quantitative co-localization
Image analysis
Texture features
Clustering
Rab proteins
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