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. © 2013 Wiley Periodicals, Inc.
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Gonzaludo, N., Zheng, H. X., Wang, J., Chanock, S. J., Jin, L., Scherer, S., … Brookes, A. J. (2013). HGV2012: Leveraging Next-Generation Technology and Large Datasets to Advance Disease Research. In Human Mutation (Vol. 34, pp. 657–660). https://doi.org/10.1002/humu.22270
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