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9/11/2014 8:39:00 PM | Browse: 517 | Download: 506
Publication Name World Journal of Gastroenterology
Manuscript ID 6029
Country/Territory Taiwan
Received
2013-09-30 08:02
Peer-Review Started
2013-09-30 17:59
To Make the First Decision
2013-10-29 12:34
Return for Revision
2013-10-30 13:26
Revised
Second Decision
2013-12-05 19:26
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief
2013-12-06 12:06
Articles in Press
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2013-12-11 11:10
Publish the Manuscript Online
2014-01-20 16:41
ISSN 1007-9327 (print) and 2219-2840 (online)
Open Access
Copyright
Article Reprints For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
Permissions For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Gastroenterology & Hepatology
Manuscript Type Topic Highlights
Article Title Target genes discovery through copy number alteration analysis in human hepatocellular carcinoma
Manuscript Source Invited Manuscript
All Author List De-Leung Gu, Yen-Hsieh Chen, Jou-Ho Shih, Chi-Hung Lin, Yuh-Shan Jou and Chian-Feng Chen
Funding Agency and Grant Number
Funding Agency Grant Number
National Research Program for Biopharmaceuticals 101-2320-B-010-066-MY3
National Science Council, Taiwan 101-2325-B-001-011
National Science Council, Taiwan 101-2320-B-001 -029-MY3
Corresponding Author Chian-Feng Chen PhD, VYM Genome Research Center, National Yang-Ming University, 155 Linong Street, Sec.2, Taipei 11221, Taiwan. cfchen@ym.edu.tw
Key Words Copy number alteration; High-density single nucleotide polymorphism arrays; Driver genes; Hepatocellular carcinoma
Core Tip In addition to detecting somatic mutations in cancer genomes with high-throughput short-read sequencing technologies, analysis of copy number alteration in hepatocellular carcinoma (HCC) cancer genomes genotyped by high density single nucleotide polymorphism arrays is a cost-effective approach to reveal genome-wide somatic alterations accumulated during tumorigenesis. Integration with other genomic data from HCC tissues derived from high-throughput short-read sequencing, proteomics, epigenomics and transcriptomics could provide lines of evidence to identify common and novel HCC genes for potential clinical applications.
Publish Date 2014-01-20 16:41
Citation Gu DL, Chen YH, Shih JH, Lin CH, Jou YS, Chen CF. Target genes discovery through copy number alteration analysis in human hepatocellular carcinoma. World J Gastroenterol 2013; 19(47): 8873-8879
URL http://www.wjgnet.com/1007-9327/full/v19/i47/8873.htm
DOI http://dx.doi.org/10.3748/wjg.v19.i47.8873
Full Article (PDF) WJG-19-8873.pdf
Manuscript File 6029-Review.docx
Answering Reviewers 6029-Answering reviewers.pdf
Copyright License Agreement 6029-Copyright assignment.pdf
Non-Native Speakers of English Editing Certificate 6029-Language certificate.pdf
Peer-review Report 6029-Peer review(s).pdf
Scientific Editor Work List 6029-Scientific editor work list.doc