Accelerate Genomics Research with the Broad-Intel Genomics
Accelerate Genomics Research with the Broad-Intel Genomics
复制标题
利用 Broad-Intel Genomics 加速基因组学研究
DOI：
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发表时间：
2017
期刊：
影响因子：
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通讯作者：
Ernesto Brau
中科院分区：
文献类型：
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作者：
Abirami Prabhakaran;Karthik Gururaj;Mishali Naik;Shiva Gopalan;Aleksandr Shargorodskiy;Ernesto Brau
基因组学正在彻底改变我们对人类生物学的理解，并为精准医学的发展做出贡献。但从历史上看，与基因组学研究相关的大量数据限制了获得新见解的速度。人类基因组测序耗时13年，耗资30亿美元;直到2012年，只有69个完整的人类基因组被测序。然而，最近多伦多大学的研究人员启动了一项庞大的项目，每年对10，000人的基因组进行测序。
Genomics is revolutionizing our understanding of human biology and contributing to the growth of precision medicine. But the sheer amount of data associated with genomics research has historically limited the pace at which new insights are obtained. It took 13 years and USD 3 billion to sequence the first human genome; as recently as 2012, only 69 whole human genomes had been sequenced. Yet, recently researchers at University of Toronto launched a massive project to sequence the genomes of 10,000 people per year.1