HerediGene 人口研究 IT 基础设施:支持基因组研究招聘和精准公共卫生的模式。

AMIA ... Annual Symposium proceedings. AMIA Symposium Pub Date : 2024-01-11 eCollection Date: 2023-01-01
David P Taylor, Bret S E Heale, Benjamin Chisum, G Bryce Christensen, Darin F Wilcox, Kevin M Banks, Jacob S Tripp, Teresa Liu, James B Ruesch, Travis J Sheffield, Jesse W Breinholt, J Clay Harward, Erin C Hakoda, Ted May, Joshua L Bonkowsky, Nephi A Walton, Howard L McLeod, Lincoln D Nadauld, Pallavi Ranade-Kharkar
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引用次数: 0

摘要

HerediGene 群体研究是一项大型研究,重点是为疾病预防、诊断、预后和新疗法的开发确定新的基因生物标志物。为了达到入选目标并将结果反馈给参与者,大量的信息技术基础设施不断发展。迄今为止,已有超过 170,000 名参与者参与了这项研究,其中 5.87% 的参与者进行了全基因组测序,0.46% 的基因分型者携带致病变异。除其他目的外,该基础设施还支持(1) 根据临床标准确定候选者,(2) 监测合格的临床事件(如抽血),(3) 联系候选者,(4) 以电子方式获得同意书,(5) 启动实验订单,(6) 将同意书和实验订单整合到临床工作流程中,(7) 解除样本和临床数据的身份识别,(8) 运送/传输样本和临床数据,(9) 对样本进行基因分型/测序,(10) 重新识别参与者身份并酌情返回结果。这项研究可作为类似基因组研究和精准公共卫生计划的典范。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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HerediGene Population Study IT infrastructure: A model to support genomic research recruitment and precision public health.

The HerediGene Population Study is a large research study focused on identifying new genetic biomarkers for disease prevention, diagnosis, prognosis, and development of new therapeutics. A substantial IT infrastructure evolved to reach enrollment targets and return results to participants. More than 170,000 participants have been enrolled in the study to date, with 5.87% of those whole genome sequenced and 0.46% of those genotyped harboring pathogenic variants. Among other purposes, this infrastructure supports: (1) identifying candidates from clinical criteria, (2) monitoring for qualifying clinical events (e.g., blood draw), (3) contacting candidates, (4) obtaining consent electronically, (5) initiating lab orders, (6) integrating consent and lab orders into clinical workflow, (7) de-identifying samples and clinical data, (8) shipping/transmitting samples and clinical data, (9) genotyping/sequencing samples, (10) and re-identifying and returning results for participants where applicable. This study may serve as a model for similar genomic research and precision public health initiatives.

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