Document Detail


HGV2012: leveraging next-generation technology and large datasets to advance disease research.
MedLine Citation:
PMID:  23315969     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The 13th International Meeting on Human Genome Variation and Complex Genome Analysis (HGV2012: Shanghai, China, 6th-8th September 2012) was a stimulating workshop where researchers from academia and industry explored the latest progress, challenges, and opportunities in genome variation research. Key themes included advancements in next-generation sequencing (NGS) technology, investigation of common and rare diseases, employing NGS in the clinic, utilizing large datasets that leverage biobanks and population-specific cohorts, and exploration of genomic features.
Authors:
Nina Gonzaludo; Hong-Xiang Zheng; Jiucun Wang; Stephen J Chanock; Li Jin; Stephen Scherer; Cisca Wijmenga; Pui-Yan Kwok; Anthony J Brookes
Related Documents :
11752729 - Ethical implications of the human-animal bond in the laboratory.
10714959 - Inhibition of ras-targeted prenylation: protein farnesyl transferase inhibitors revisited.
17470069 - Ethical stockmanship.
16830689 - Education and research in biomedical engineering of the budapest university of technolo...
11182899 - problems of animal experimentation - reflections and practical approaches
18288429 - A survey concerning the work of ethics committees and licensing authorities for animal ...
20614119 - The weakness of tight ties: why scientists almost destroyed the coachella valley multis...
392909 - Research on viral hepatitis performed in the "stefan s. nicolau" institute of virology.
17729559 - Mission-oriented research for light machinery.
Publication Detail:
Type:  Congresses; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Human mutation     Volume:  34     ISSN:  1098-1004     ISO Abbreviation:  Hum. Mutat.     Publication Date:  2013 Apr 
Date Detail:
Created Date:  2013-03-22     Completed Date:  2013-09-06     Revised Date:  2014-04-02    
Medline Journal Info:
Nlm Unique ID:  9215429     Medline TA:  Hum Mutat     Country:  United States    
Other Details:
Languages:  eng     Pagination:  657-60     Citation Subset:  IM    
Copyright Information:
© 2013 Wiley Periodicals, Inc.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Genetic Testing*
Genome-Wide Association Study*
Genomics
High-Throughput Nucleotide Sequencing*
Humans
Grant Support
ID/Acronym/Agency:
R13 HG003953/HG/NHGRI NIH HHS; R13 HG003953/HG/NHGRI NIH HHS; T32 GM007175/GM/NIGMS NIH HHS; T32 GM007175/GM/NIGMS NIH HHS
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Hepatocyte nuclear factor 4 alpha deletion promotes diethylnitrosamine-induced hepatocellular carcin...
Next Document:  Influence of relative humidity on analyzing electric field exposure using ELF electric field measure...