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Sample entropy analysis of cervical neoplasia gene-expression signatures

BACKGROUND: We introduce Approximate Entropy as a mathematical method of analysis for microarray data. Approximate entropy is applied here as a method to classify the complex gene expression patterns resultant of a clinical sample set. Since Entropy is a measure of disorder in a system, we believe t...

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Autores principales: Botting, Shaleen K, Trzeciakowski, Jerome P, Benoit, Michelle F, Salama, Salama A, Diaz-Arrastia, Concepcion R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656476/
https://www.ncbi.nlm.nih.gov/pubmed/19232110
http://dx.doi.org/10.1186/1471-2105-10-66
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author Botting, Shaleen K
Trzeciakowski, Jerome P
Benoit, Michelle F
Salama, Salama A
Diaz-Arrastia, Concepcion R
author_facet Botting, Shaleen K
Trzeciakowski, Jerome P
Benoit, Michelle F
Salama, Salama A
Diaz-Arrastia, Concepcion R
author_sort Botting, Shaleen K
collection PubMed
description BACKGROUND: We introduce Approximate Entropy as a mathematical method of analysis for microarray data. Approximate entropy is applied here as a method to classify the complex gene expression patterns resultant of a clinical sample set. Since Entropy is a measure of disorder in a system, we believe that by choosing genes which display minimum entropy in normal controls and maximum entropy in the cancerous sample set we will be able to distinguish those genes which display the greatest variability in the cancerous set. Here we describe a method of utilizing Approximate Sample Entropy (ApSE) analysis to identify genes of interest with the highest probability of producing an accurate, predictive, classification model from our data set. RESULTS: In the development of a diagnostic gene-expression profile for cervical intraepithelial neoplasia (CIN) and squamous cell carcinoma of the cervix, we identified 208 genes which are unchanging in all normal tissue samples, yet exhibit a random pattern indicative of the genetic instability and heterogeneity of malignant cells. This may be measured in terms of the ApSE when compared to normal tissue. We have validated 10 of these genes on 10 Normal and 20 cancer and CIN3 samples. We report that the predictive value of the sample entropy calculation for these 10 genes of interest is promising (75% sensitivity, 80% specificity for prediction of cervical cancer over CIN3). CONCLUSION: The success of the Approximate Sample Entropy approach in discerning alterations in complexity from biological system with such relatively small sample set, and extracting biologically relevant genes of interest hold great promise.
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spelling pubmed-26564762009-03-17 Sample entropy analysis of cervical neoplasia gene-expression signatures Botting, Shaleen K Trzeciakowski, Jerome P Benoit, Michelle F Salama, Salama A Diaz-Arrastia, Concepcion R BMC Bioinformatics Research Article BACKGROUND: We introduce Approximate Entropy as a mathematical method of analysis for microarray data. Approximate entropy is applied here as a method to classify the complex gene expression patterns resultant of a clinical sample set. Since Entropy is a measure of disorder in a system, we believe that by choosing genes which display minimum entropy in normal controls and maximum entropy in the cancerous sample set we will be able to distinguish those genes which display the greatest variability in the cancerous set. Here we describe a method of utilizing Approximate Sample Entropy (ApSE) analysis to identify genes of interest with the highest probability of producing an accurate, predictive, classification model from our data set. RESULTS: In the development of a diagnostic gene-expression profile for cervical intraepithelial neoplasia (CIN) and squamous cell carcinoma of the cervix, we identified 208 genes which are unchanging in all normal tissue samples, yet exhibit a random pattern indicative of the genetic instability and heterogeneity of malignant cells. This may be measured in terms of the ApSE when compared to normal tissue. We have validated 10 of these genes on 10 Normal and 20 cancer and CIN3 samples. We report that the predictive value of the sample entropy calculation for these 10 genes of interest is promising (75% sensitivity, 80% specificity for prediction of cervical cancer over CIN3). CONCLUSION: The success of the Approximate Sample Entropy approach in discerning alterations in complexity from biological system with such relatively small sample set, and extracting biologically relevant genes of interest hold great promise. BioMed Central 2009-02-20 /pmc/articles/PMC2656476/ /pubmed/19232110 http://dx.doi.org/10.1186/1471-2105-10-66 Text en Copyright © 2009 Botting 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
Botting, Shaleen K
Trzeciakowski, Jerome P
Benoit, Michelle F
Salama, Salama A
Diaz-Arrastia, Concepcion R
Sample entropy analysis of cervical neoplasia gene-expression signatures
title Sample entropy analysis of cervical neoplasia gene-expression signatures
title_full Sample entropy analysis of cervical neoplasia gene-expression signatures
title_fullStr Sample entropy analysis of cervical neoplasia gene-expression signatures
title_full_unstemmed Sample entropy analysis of cervical neoplasia gene-expression signatures
title_short Sample entropy analysis of cervical neoplasia gene-expression signatures
title_sort sample entropy analysis of cervical neoplasia gene-expression signatures
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656476/
https://www.ncbi.nlm.nih.gov/pubmed/19232110
http://dx.doi.org/10.1186/1471-2105-10-66
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