国际HapMap项目中的社区参与和知情同意。

Charles Rotimi, Mark Leppert, Ichiro Matsuda, Changqing Zeng, Houcan Zhang, Clement Adebamowo, Ike Ajayi, Toyin Aniagwu, Missy Dixon, Yoshimitsu Fukushima, Darryl Macer, Patricia Marshall, Chibuzor Nkwodimmah, Andy Peiffer, Charmaine Royal, Eiko Suda, Hui Zhao, Vivian Ota Wang, Jean McEwen
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引用次数: 73

摘要

国际单体型图联盟开发了单体型图,这是一个描述人类遗传变异(单体型)共同模式的资源。在每个收集样本的地方实施了社区/公众咨询和个人知情同意的过程,以了解并试图解决个人和群体关注的问题。人们对这项研究的看法各不相同,但我们没有发现对这项研究的批评。纳入社区投入和回应所提出的关切是具有挑战性的。然而,经验表明,以开放的精神进行遗传变异研究可以帮助研究人员更好地欣赏他们寻求研究样本的社区的观点,并帮助社区更多地参与科学研究。
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Community engagement and informed consent in the International HapMap project.

The International HapMap Consortium has developed the HapMap, a resource that describes the common patterns of human genetic variation (haplotypes). Processes of community/public consultation and individual informed consent were implemented in each locality where samples were collected to understand and attempt to address both individual and group concerns. Perceptions about the research varied, but we detected no critical opposition to the research. Incorporating community input and responding to concerns raised was challenging. However, the experience suggests that approaching genetic variation research in a spirit of openness can help investigators better appreciate the views of the communities whose samples they seek to study and help communities become more engaged in the science.

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