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cellXpress: a fast and user-friendly software platform for profiling cellular phenotypes

BACKGROUND: High-throughput, image-based screens of cellular responses to genetic or chemical perturbations generate huge numbers of cell images. Automated analysis is required to quantify and compare the effects of these perturbations. However, few of the current freely-available bioimage analysis...

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Autores principales: Laksameethanasan, Danai, Tan, Rui Zhen, Toh, Geraldine Wei-Ling, Loo, Lit-Hsin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853218/
https://www.ncbi.nlm.nih.gov/pubmed/24564609
http://dx.doi.org/10.1186/1471-2105-14-S16-S4
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author Laksameethanasan, Danai
Tan, Rui Zhen
Toh, Geraldine Wei-Ling
Loo, Lit-Hsin
author_facet Laksameethanasan, Danai
Tan, Rui Zhen
Toh, Geraldine Wei-Ling
Loo, Lit-Hsin
author_sort Laksameethanasan, Danai
collection PubMed
description BACKGROUND: High-throughput, image-based screens of cellular responses to genetic or chemical perturbations generate huge numbers of cell images. Automated analysis is required to quantify and compare the effects of these perturbations. However, few of the current freely-available bioimage analysis software tools are optimized for efficient handling of these images. Even fewer of them are designed to transform the phenotypic features measured from these images into discriminative profiles that can reveal biologically meaningful associations among the tested perturbations. RESULTS: We present a fast and user-friendly software platform called "cellXpress" to segment cells, measure quantitative features of cellular phenotypes, construct discriminative profiles, and visualize the resulting cell masks and feature values. We have also developed a suite of library functions to load the extracted features for further customizable analysis and visualization under the R computing environment. We systematically compared the processing speed, cell segmentation accuracy, and phenotypic-profile clustering performance of cellXpress to other existing bioimage analysis software packages or algorithms. We found that cellXpress outperforms these existing tools on three different bioimage datasets. We estimate that cellXpress could finish processing a genome-wide gene knockdown image dataset in less than a day on a modern personal desktop computer. CONCLUSIONS: The cellXpress platform is designed to make fast and efficient high-throughput phenotypic profiling more accessible to the wider biological research community. The cellXpress installation packages for 64-bit Windows and Linux, user manual, installation guide, and datasets used in this analysis can be downloaded freely from http://www.cellXpress.org.
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spelling pubmed-38532182013-12-18 cellXpress: a fast and user-friendly software platform for profiling cellular phenotypes Laksameethanasan, Danai Tan, Rui Zhen Toh, Geraldine Wei-Ling Loo, Lit-Hsin BMC Bioinformatics Research BACKGROUND: High-throughput, image-based screens of cellular responses to genetic or chemical perturbations generate huge numbers of cell images. Automated analysis is required to quantify and compare the effects of these perturbations. However, few of the current freely-available bioimage analysis software tools are optimized for efficient handling of these images. Even fewer of them are designed to transform the phenotypic features measured from these images into discriminative profiles that can reveal biologically meaningful associations among the tested perturbations. RESULTS: We present a fast and user-friendly software platform called "cellXpress" to segment cells, measure quantitative features of cellular phenotypes, construct discriminative profiles, and visualize the resulting cell masks and feature values. We have also developed a suite of library functions to load the extracted features for further customizable analysis and visualization under the R computing environment. We systematically compared the processing speed, cell segmentation accuracy, and phenotypic-profile clustering performance of cellXpress to other existing bioimage analysis software packages or algorithms. We found that cellXpress outperforms these existing tools on three different bioimage datasets. We estimate that cellXpress could finish processing a genome-wide gene knockdown image dataset in less than a day on a modern personal desktop computer. CONCLUSIONS: The cellXpress platform is designed to make fast and efficient high-throughput phenotypic profiling more accessible to the wider biological research community. The cellXpress installation packages for 64-bit Windows and Linux, user manual, installation guide, and datasets used in this analysis can be downloaded freely from http://www.cellXpress.org. BioMed Central 2013-10-22 /pmc/articles/PMC3853218/ /pubmed/24564609 http://dx.doi.org/10.1186/1471-2105-14-S16-S4 Text en Copyright © 2013 Laksameethanasan 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
Laksameethanasan, Danai
Tan, Rui Zhen
Toh, Geraldine Wei-Ling
Loo, Lit-Hsin
cellXpress: a fast and user-friendly software platform for profiling cellular phenotypes
title cellXpress: a fast and user-friendly software platform for profiling cellular phenotypes
title_full cellXpress: a fast and user-friendly software platform for profiling cellular phenotypes
title_fullStr cellXpress: a fast and user-friendly software platform for profiling cellular phenotypes
title_full_unstemmed cellXpress: a fast and user-friendly software platform for profiling cellular phenotypes
title_short cellXpress: a fast and user-friendly software platform for profiling cellular phenotypes
title_sort cellxpress: a fast and user-friendly software platform for profiling cellular phenotypes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853218/
https://www.ncbi.nlm.nih.gov/pubmed/24564609
http://dx.doi.org/10.1186/1471-2105-14-S16-S4
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