部署危险DNA的数字检测

Hanna Pálya, Oscar Delaney
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摘要

近几十年来,随时可以获得合成DNA使卫生和生物技术取得了巨大进展。然而,这也使恶意行为者更容易开发威胁公众健康的生物武器。因此,规范谁可以从商业供应商处订购病原体的合成DNA是至关重要的。一些合成DNA供应商筛选客户和排序序列;然而,没有联邦立法规定这些公司的责任。自愿遵守美国卫生与公众服务部(HHS)发布的筛查指南是不可持续的,因为它使进行筛查的公司与不进行筛查的公司处于不利地位。在这里,我们考虑两种政策解决方案。选项1是对所有美国合成DNA提供者强制执行最低筛选标准。这种监管负担可能会削弱美国的DNA合成部门,因此我们建议选择2,即要求政府资助的研究人员只使用经过认证的符合筛选要求的供应商的合成DNA。
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Deploying Digital Detection of Dangerous DNA
Ready access to synthetic DNA has enabled vast progress in health and biotechnology in recent decades. However, it also makes it easier for malicious actors to develop biological weapons that threaten public health. Thus, it is crucial to regulate who can order synthetic DNA of pathogens from commercial providers. Some synthetic DNA providers screen customers and ordered sequences; however, there is no federal legislation addressing the responsibilities of these companies. Voluntary compliance with the screening Guidance issued by the US Department of Health and Human Services (HHS) is not sustainable, as it disadvantages companies who screen against those who do not. Here, we consider two policy solutions. Option 1 is to mandate minimum screening standards for all US-based synthetic DNA providers. This regulatory burden may weaken the US DNA synthesis sector, so we recommend Option 2, which requires government-funded researchers to only use synthetic DNA from accredited screening-compliant providers.
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