PGTandMe: social networking-based genetic testing and the evolving research model.

Valerie Gutmann Koch
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Abstract

The opportunity to use extensive genetic data, personal information, and family medical history for research purposes may be naturally appealing to the personal genetic testing (PGT) industry, which is already coupling direct-to-consumer (DTC) products with social networking technologies, as well as to potential industry or institutional partners. This article evaluates the transformation in research that the hybrid of PGT and social networking will bring about, and--highlighting the challenges associated with a new paradigm of "patient-driven" genomic research--focuses on the consequences of shifting the structure, locus, timing, and scope of research through genetic crowd-sourcing. This article also explores potential ethical, legal, and regulatory issues that arise from the hybrid between personal genomic research and online social networking, particularly regarding informed consent, institutional review board (IRB) oversight, and ownership/intellectual property (IP) considerations.

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PGTandMe:基于社会网络的基因检测和不断发展的研究模式。
利用广泛的基因数据、个人信息和家族病史进行研究的机会自然会吸引个人基因检测(PGT)行业,该行业已经将直接面向消费者(DTC)的产品与社交网络技术结合起来,同时也吸引了潜在的行业或机构合作伙伴。本文评估了PGT和社交网络的混合将带来的研究转变,并强调了与“患者驱动”基因组研究新范式相关的挑战,重点关注了通过基因众包改变研究结构、位点、时间和范围的后果。本文还探讨了个人基因组研究与在线社交网络相结合所产生的潜在伦理、法律和监管问题,特别是在知情同意、机构审查委员会(IRB)监督和所有权/知识产权(IP)考虑方面。
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