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Exploring cancer genomic data from the cancer genome atlas project
The Cancer Genome Atlas (TCGA) has compiled genomic, epigenomic, and proteomic data from more than 10,000 samples derived from 33 types of cancer, aiming to improve our understanding of the molecular basis of cancer development. Availability of these genome-wide information provides an unprecedented...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Society for Biochemistry and Molecular Biology
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346320/ https://www.ncbi.nlm.nih.gov/pubmed/27530686 http://dx.doi.org/10.5483/BMBRep.2016.49.11.145 |
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author | Lee, Ju-Seog |
author_facet | Lee, Ju-Seog |
author_sort | Lee, Ju-Seog |
collection | PubMed |
description | The Cancer Genome Atlas (TCGA) has compiled genomic, epigenomic, and proteomic data from more than 10,000 samples derived from 33 types of cancer, aiming to improve our understanding of the molecular basis of cancer development. Availability of these genome-wide information provides an unprecedented opportunity for uncovering new key regulators of signaling pathways or new roles of pre-existing members in pathways. To take advantage of the advancement, it will be necessary to learn systematic approaches that can help to uncover novel genes reflecting genetic alterations, prognosis, or response to treatments. This minireview describes the updated status of TCGA project and explains how to use TCGA data. |
format | Online Article Text |
id | pubmed-5346320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-53463202017-04-06 Exploring cancer genomic data from the cancer genome atlas project Lee, Ju-Seog BMB Rep Invited Mini Review The Cancer Genome Atlas (TCGA) has compiled genomic, epigenomic, and proteomic data from more than 10,000 samples derived from 33 types of cancer, aiming to improve our understanding of the molecular basis of cancer development. Availability of these genome-wide information provides an unprecedented opportunity for uncovering new key regulators of signaling pathways or new roles of pre-existing members in pathways. To take advantage of the advancement, it will be necessary to learn systematic approaches that can help to uncover novel genes reflecting genetic alterations, prognosis, or response to treatments. This minireview describes the updated status of TCGA project and explains how to use TCGA data. Korean Society for Biochemistry and Molecular Biology 2016 2016-11-30 /pmc/articles/PMC5346320/ /pubmed/27530686 http://dx.doi.org/10.5483/BMBRep.2016.49.11.145 Text en Copyright © 2016 by the The Korean Society for Biochemistry and Molecular Biology http://creativecommons.org/licenses/by-nc/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Invited Mini Review Lee, Ju-Seog Exploring cancer genomic data from the cancer genome atlas project |
title | Exploring cancer genomic data from the cancer genome atlas project |
title_full | Exploring cancer genomic data from the cancer genome atlas project |
title_fullStr | Exploring cancer genomic data from the cancer genome atlas project |
title_full_unstemmed | Exploring cancer genomic data from the cancer genome atlas project |
title_short | Exploring cancer genomic data from the cancer genome atlas project |
title_sort | exploring cancer genomic data from the cancer genome atlas project |
topic | Invited Mini Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346320/ https://www.ncbi.nlm.nih.gov/pubmed/27530686 http://dx.doi.org/10.5483/BMBRep.2016.49.11.145 |
work_keys_str_mv | AT leejuseog exploringcancergenomicdatafromthecancergenomeatlasproject |