CaGe: A Web-Based Cancer Gene Annotation System for Cancer Genomics

High-throughput genomic technologies (HGTs), including next-generation DNA sequencing (NGS), microarray, and serial analysis of gene expression (SAGE), have become effective experimental tools for cancer genomics to identify cancer-associated somatic genomic alterations and genes. The main hurdle in...

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Main Authors: Young-Kyu Park, Tae-Wook Kang, Su-Jin Baek, Kwon-Il Kim, Seon-Young Kim, Doheon Lee, Yong Sung Kim
Format: Article
Language:English
Published: BioMed Central 2012-03-01
Series:Genomics & Informatics
Subjects:
Online Access:http://genominfo.org/upload/pdf/gni-10-33.pdf
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author Young-Kyu Park
Tae-Wook Kang
Su-Jin Baek
Kwon-Il Kim
Seon-Young Kim
Doheon Lee
Yong Sung Kim
author_facet Young-Kyu Park
Tae-Wook Kang
Su-Jin Baek
Kwon-Il Kim
Seon-Young Kim
Doheon Lee
Yong Sung Kim
author_sort Young-Kyu Park
collection DOAJ
description High-throughput genomic technologies (HGTs), including next-generation DNA sequencing (NGS), microarray, and serial analysis of gene expression (SAGE), have become effective experimental tools for cancer genomics to identify cancer-associated somatic genomic alterations and genes. The main hurdle in cancer genomics is to identify the real causative mutations or genes out of many candidates from an HGT-based cancer genomic analysis. One useful approach is to refer to known cancer genes and associated information. The list of known cancer genes can be used to determine candidates of cancer driver mutations, while cancer gene-related information, including gene expression, protein-protein interaction, and pathways, can be useful for scoring novel candidates. Some cancer gene or mutation databases exist for this purpose, but few specialized tools exist for an automated analysis of a long gene list from an HGT-based cancer genomic analysis. This report presents a new web-accessible bioinformatic tool, called CaGe, a cancer genome annotation system for the assessment of candidates of cancer genes from HGT-based cancer genomics. The tool provides users with information on cancer-related genes, mutations, pathways, and associated annotations through annotation and browsing functions. With this tool, researchers can classify their candidate genes from cancer genome studies into either previously reported or novel categories of cancer genes and gain insight into underlying carcinogenic mechanisms through a pathway analysis. We show the usefulness of CaGe by assessing its performance in annotating somatic mutations from a published small cell lung cancer study.
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spelling doaj-art-edb0c5f1d55f42879c5a800c6d193ae32025-02-02T21:22:21ZengBioMed CentralGenomics & Informatics1598-866X2234-07422012-03-01101333910.5808/GI.2012.10.1.3329CaGe: A Web-Based Cancer Gene Annotation System for Cancer GenomicsYoung-Kyu Park0Tae-Wook Kang1Su-Jin Baek2Kwon-Il Kim3Seon-Young Kim4Doheon Lee5Yong Sung Kim6Medical Genomics Research Center, KRIBB, Daejeon 305-806, Korea.Medical Genomics Research Center, KRIBB, Daejeon 305-806, Korea.Medical Genomics Research Center, KRIBB, Daejeon 305-806, Korea.Department of Bio and Brain Engineering, KAIST, Daejeon 305-701, Korea.Medical Genomics Research Center, KRIBB, Daejeon 305-806, Korea.Department of Bio and Brain Engineering, KAIST, Daejeon 305-701, Korea.Medical Genomics Research Center, KRIBB, Daejeon 305-806, Korea.High-throughput genomic technologies (HGTs), including next-generation DNA sequencing (NGS), microarray, and serial analysis of gene expression (SAGE), have become effective experimental tools for cancer genomics to identify cancer-associated somatic genomic alterations and genes. The main hurdle in cancer genomics is to identify the real causative mutations or genes out of many candidates from an HGT-based cancer genomic analysis. One useful approach is to refer to known cancer genes and associated information. The list of known cancer genes can be used to determine candidates of cancer driver mutations, while cancer gene-related information, including gene expression, protein-protein interaction, and pathways, can be useful for scoring novel candidates. Some cancer gene or mutation databases exist for this purpose, but few specialized tools exist for an automated analysis of a long gene list from an HGT-based cancer genomic analysis. This report presents a new web-accessible bioinformatic tool, called CaGe, a cancer genome annotation system for the assessment of candidates of cancer genes from HGT-based cancer genomics. The tool provides users with information on cancer-related genes, mutations, pathways, and associated annotations through annotation and browsing functions. With this tool, researchers can classify their candidate genes from cancer genome studies into either previously reported or novel categories of cancer genes and gain insight into underlying carcinogenic mechanisms through a pathway analysis. We show the usefulness of CaGe by assessing its performance in annotating somatic mutations from a published small cell lung cancer study.http://genominfo.org/upload/pdf/gni-10-33.pdfannotationcancer genehigh-throughput genomic technologymutationnext-generation sequencingpathway
spellingShingle Young-Kyu Park
Tae-Wook Kang
Su-Jin Baek
Kwon-Il Kim
Seon-Young Kim
Doheon Lee
Yong Sung Kim
CaGe: A Web-Based Cancer Gene Annotation System for Cancer Genomics
Genomics & Informatics
annotation
cancer gene
high-throughput genomic technology
mutation
next-generation sequencing
pathway
title CaGe: A Web-Based Cancer Gene Annotation System for Cancer Genomics
title_full CaGe: A Web-Based Cancer Gene Annotation System for Cancer Genomics
title_fullStr CaGe: A Web-Based Cancer Gene Annotation System for Cancer Genomics
title_full_unstemmed CaGe: A Web-Based Cancer Gene Annotation System for Cancer Genomics
title_short CaGe: A Web-Based Cancer Gene Annotation System for Cancer Genomics
title_sort cage a web based cancer gene annotation system for cancer genomics
topic annotation
cancer gene
high-throughput genomic technology
mutation
next-generation sequencing
pathway
url http://genominfo.org/upload/pdf/gni-10-33.pdf
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