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- [www.ncbi.nlm.nih.gov] | PDF
- [europepmc.org] | PDF
- [www.researchgate.net] | PDF
- [www.ncbi.nlm.nih.gov] | PDF
- [www.ncbi.nlm.nih.gov] | PDF
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HGV2012: Leveraging Next-Generation Technology and Large Datasets to Advance Disease Research
Journal article published in 2013 by
Nina Gonzaludo,
Hong-Xiang Zheng,
Jiucun Wang,
Stephen J. Chanock,
Li Jin 
,
Stephen Scherer,
Cisca Wijmenga ,
Pui-Yan Kwok,
Anthony J. Brookes
,
Stephen Scherer,
Cisca Wijmenga ,
Pui-Yan Kwok,
Anthony J. Brookes
Abstract
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.