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Breast Cancer Prognostics Using Multi-Omics Data

Breast cancer affects one in eight women in America and is a leading cause of death from cancer worldwide. In the current study, four types of Omics data including copy number variation, gene expression, proteome and phosphoproteome were collected from seventy-seven breast cancer patients. Individua...

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Detalles Bibliográficos
Autores principales: Ma, Sisi, Ren, Jiwen, Fenyö, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Informatics Association 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5001766/
https://www.ncbi.nlm.nih.gov/pubmed/27570650
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author Ma, Sisi
Ren, Jiwen
Fenyö, David
author_facet Ma, Sisi
Ren, Jiwen
Fenyö, David
author_sort Ma, Sisi
collection PubMed
description Breast cancer affects one in eight women in America and is a leading cause of death from cancer worldwide. In the current study, four types of Omics data including copy number variation, gene expression, proteome and phosphoproteome were collected from seventy-seven breast cancer patients. Individual types of Omics data were used to separately construct predictive models to predict ten-year survival, an important clinical hallmark. The predictive models constructed with proteome data achieved decent predictivity (mean AUC = 0.725) and outperforms the models constructed with other types of Omics data. This indicates that high quality, large scale protein data is more effective for survival prediction compared to other types of omics data. Further, we experimented with ten different data fusion techniques (generic and Multi-kernel learning based) to test whether combining multi-Omics data can result in improved predictive performance. None of the data fusion techniques tested in the current study outperforms the predictive models built with the proteome data.
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spelling pubmed-50017662016-08-26 Breast Cancer Prognostics Using Multi-Omics Data Ma, Sisi Ren, Jiwen Fenyö, David AMIA Jt Summits Transl Sci Proc Articles Breast cancer affects one in eight women in America and is a leading cause of death from cancer worldwide. In the current study, four types of Omics data including copy number variation, gene expression, proteome and phosphoproteome were collected from seventy-seven breast cancer patients. Individual types of Omics data were used to separately construct predictive models to predict ten-year survival, an important clinical hallmark. The predictive models constructed with proteome data achieved decent predictivity (mean AUC = 0.725) and outperforms the models constructed with other types of Omics data. This indicates that high quality, large scale protein data is more effective for survival prediction compared to other types of omics data. Further, we experimented with ten different data fusion techniques (generic and Multi-kernel learning based) to test whether combining multi-Omics data can result in improved predictive performance. None of the data fusion techniques tested in the current study outperforms the predictive models built with the proteome data. American Medical Informatics Association 2016-07-20 /pmc/articles/PMC5001766/ /pubmed/27570650 Text en ©2016 AMIA - All rights reserved. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose
spellingShingle Articles
Ma, Sisi
Ren, Jiwen
Fenyö, David
Breast Cancer Prognostics Using Multi-Omics Data
title Breast Cancer Prognostics Using Multi-Omics Data
title_full Breast Cancer Prognostics Using Multi-Omics Data
title_fullStr Breast Cancer Prognostics Using Multi-Omics Data
title_full_unstemmed Breast Cancer Prognostics Using Multi-Omics Data
title_short Breast Cancer Prognostics Using Multi-Omics Data
title_sort breast cancer prognostics using multi-omics data
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5001766/
https://www.ncbi.nlm.nih.gov/pubmed/27570650
work_keys_str_mv AT masisi breastcancerprognosticsusingmultiomicsdata
AT renjiwen breastcancerprognosticsusingmultiomicsdata
AT fenyodavid breastcancerprognosticsusingmultiomicsdata