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Integrative computational biology for cancer research

Over the past two decades, high-throughput (HTP) technologies such as microarrays and mass spectrometry have fundamentally changed clinical cancer research. They have revealed novel molecular markers of cancer subtypes, metastasis, and drug sensitivity and resistance. Some have been translated into...

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Detalles Bibliográficos
Autores principales: Fortney, Kristen, Jurisica, Igor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3179275/
https://www.ncbi.nlm.nih.gov/pubmed/21691773
http://dx.doi.org/10.1007/s00439-011-0983-z
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author Fortney, Kristen
Jurisica, Igor
author_facet Fortney, Kristen
Jurisica, Igor
author_sort Fortney, Kristen
collection PubMed
description Over the past two decades, high-throughput (HTP) technologies such as microarrays and mass spectrometry have fundamentally changed clinical cancer research. They have revealed novel molecular markers of cancer subtypes, metastasis, and drug sensitivity and resistance. Some have been translated into the clinic as tools for early disease diagnosis, prognosis, and individualized treatment and response monitoring. Despite these successes, many challenges remain: HTP platforms are often noisy and suffer from false positives and false negatives; optimal analysis and successful validation require complex workflows; and great volumes of data are accumulating at a rapid pace. Here we discuss these challenges, and show how integrative computational biology can help diminish them by creating new software tools, analytical methods, and data standards. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00439-011-0983-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-31792752011-09-30 Integrative computational biology for cancer research Fortney, Kristen Jurisica, Igor Hum Genet Review Paper Over the past two decades, high-throughput (HTP) technologies such as microarrays and mass spectrometry have fundamentally changed clinical cancer research. They have revealed novel molecular markers of cancer subtypes, metastasis, and drug sensitivity and resistance. Some have been translated into the clinic as tools for early disease diagnosis, prognosis, and individualized treatment and response monitoring. Despite these successes, many challenges remain: HTP platforms are often noisy and suffer from false positives and false negatives; optimal analysis and successful validation require complex workflows; and great volumes of data are accumulating at a rapid pace. Here we discuss these challenges, and show how integrative computational biology can help diminish them by creating new software tools, analytical methods, and data standards. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00439-011-0983-z) contains supplementary material, which is available to authorized users. Springer-Verlag 2011-04-22 2011 /pmc/articles/PMC3179275/ /pubmed/21691773 http://dx.doi.org/10.1007/s00439-011-0983-z Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Review Paper
Fortney, Kristen
Jurisica, Igor
Integrative computational biology for cancer research
title Integrative computational biology for cancer research
title_full Integrative computational biology for cancer research
title_fullStr Integrative computational biology for cancer research
title_full_unstemmed Integrative computational biology for cancer research
title_short Integrative computational biology for cancer research
title_sort integrative computational biology for cancer research
topic Review Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3179275/
https://www.ncbi.nlm.nih.gov/pubmed/21691773
http://dx.doi.org/10.1007/s00439-011-0983-z
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