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Bioinformatics challenges for personalized medicine
Motivation: Widespread availability of low-cost, full genome sequencing will introduce new challenges for bioinformatics. Results: This review outlines recent developments in sequencing technologies and genome analysis methods for application in personalized medicine. New methods are needed in four...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117361/ https://www.ncbi.nlm.nih.gov/pubmed/21596790 http://dx.doi.org/10.1093/bioinformatics/btr295 |
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author | Fernald, Guy Haskin Capriotti, Emidio Daneshjou, Roxana Karczewski, Konrad J. Altman, Russ B. |
author_facet | Fernald, Guy Haskin Capriotti, Emidio Daneshjou, Roxana Karczewski, Konrad J. Altman, Russ B. |
author_sort | Fernald, Guy Haskin |
collection | PubMed |
description | Motivation: Widespread availability of low-cost, full genome sequencing will introduce new challenges for bioinformatics. Results: This review outlines recent developments in sequencing technologies and genome analysis methods for application in personalized medicine. New methods are needed in four areas to realize the potential of personalized medicine: (i) processing large-scale robust genomic data; (ii) interpreting the functional effect and the impact of genomic variation; (iii) integrating systems data to relate complex genetic interactions with phenotypes; and (iv) translating these discoveries into medical practice. Contact: russ.altman@stanford.edu Supplementary information: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-3117361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-31173612011-06-17 Bioinformatics challenges for personalized medicine Fernald, Guy Haskin Capriotti, Emidio Daneshjou, Roxana Karczewski, Konrad J. Altman, Russ B. Bioinformatics Review Motivation: Widespread availability of low-cost, full genome sequencing will introduce new challenges for bioinformatics. Results: This review outlines recent developments in sequencing technologies and genome analysis methods for application in personalized medicine. New methods are needed in four areas to realize the potential of personalized medicine: (i) processing large-scale robust genomic data; (ii) interpreting the functional effect and the impact of genomic variation; (iii) integrating systems data to relate complex genetic interactions with phenotypes; and (iv) translating these discoveries into medical practice. Contact: russ.altman@stanford.edu Supplementary information: Supplementary data are available at Bioinformatics online. Oxford University Press 2011-07-01 2011-05-19 /pmc/articles/PMC3117361/ /pubmed/21596790 http://dx.doi.org/10.1093/bioinformatics/btr295 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Fernald, Guy Haskin Capriotti, Emidio Daneshjou, Roxana Karczewski, Konrad J. Altman, Russ B. Bioinformatics challenges for personalized medicine |
title | Bioinformatics challenges for personalized medicine |
title_full | Bioinformatics challenges for personalized medicine |
title_fullStr | Bioinformatics challenges for personalized medicine |
title_full_unstemmed | Bioinformatics challenges for personalized medicine |
title_short | Bioinformatics challenges for personalized medicine |
title_sort | bioinformatics challenges for personalized medicine |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117361/ https://www.ncbi.nlm.nih.gov/pubmed/21596790 http://dx.doi.org/10.1093/bioinformatics/btr295 |
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