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Multiclass discovery in array data

BACKGROUND: A routine goal in the analysis of microarray data is to identify genes with expression levels that correlate with known classes of experiments. In a growing number of array data sets, it has been shown that there is an over-abundance of genes that discriminate between known classes as co...

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Detalles Bibliográficos
Autores principales: Liu, Yingchun, Ringnér, Markus
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC434495/
https://www.ncbi.nlm.nih.gov/pubmed/15180908
http://dx.doi.org/10.1186/1471-2105-5-70
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author Liu, Yingchun
Ringnér, Markus
author_facet Liu, Yingchun
Ringnér, Markus
author_sort Liu, Yingchun
collection PubMed
description BACKGROUND: A routine goal in the analysis of microarray data is to identify genes with expression levels that correlate with known classes of experiments. In a growing number of array data sets, it has been shown that there is an over-abundance of genes that discriminate between known classes as compared to expectations for random classes. Therefore, one can search for novel classes in array data by looking for partitions of experiments for which there are an over-abundance of discriminatory genes. We have previously used such an approach in a breast cancer study. RESULTS: We describe the implementation of an unsupervised classification method for class discovery in microarray data. The method allows for discovery of more than two classes. We applied our method on two published microarray data sets: small round blue cell tumors and breast tumors. The method predicts relevant classes in the data sets with high success rates. CONCLUSIONS: We conclude that the proposed method is accurate and efficient in finding biologically relevant classes in microarray data. Additionally, the method is useful for quality control of microarray experiments. We have made the method available as a computer program.
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spelling pubmed-4344952004-06-25 Multiclass discovery in array data Liu, Yingchun Ringnér, Markus BMC Bioinformatics Software BACKGROUND: A routine goal in the analysis of microarray data is to identify genes with expression levels that correlate with known classes of experiments. In a growing number of array data sets, it has been shown that there is an over-abundance of genes that discriminate between known classes as compared to expectations for random classes. Therefore, one can search for novel classes in array data by looking for partitions of experiments for which there are an over-abundance of discriminatory genes. We have previously used such an approach in a breast cancer study. RESULTS: We describe the implementation of an unsupervised classification method for class discovery in microarray data. The method allows for discovery of more than two classes. We applied our method on two published microarray data sets: small round blue cell tumors and breast tumors. The method predicts relevant classes in the data sets with high success rates. CONCLUSIONS: We conclude that the proposed method is accurate and efficient in finding biologically relevant classes in microarray data. Additionally, the method is useful for quality control of microarray experiments. We have made the method available as a computer program. BioMed Central 2004-06-04 /pmc/articles/PMC434495/ /pubmed/15180908 http://dx.doi.org/10.1186/1471-2105-5-70 Text en Copyright © 2004 Liu and Ringnér; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Software
Liu, Yingchun
Ringnér, Markus
Multiclass discovery in array data
title Multiclass discovery in array data
title_full Multiclass discovery in array data
title_fullStr Multiclass discovery in array data
title_full_unstemmed Multiclass discovery in array data
title_short Multiclass discovery in array data
title_sort multiclass discovery in array data
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC434495/
https://www.ncbi.nlm.nih.gov/pubmed/15180908
http://dx.doi.org/10.1186/1471-2105-5-70
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