Symposium on Advances in Genomics, Epidemiology, and Statistics (SAGES)

摘要 技术的进步和成本的显著降低正在推动基因组研究的进步。的研究 在大样本中，复杂性状的整个外显子组和基因组序列越来越常见。其他 高维信息的来源，包括表达、表观遗传、代谢和微生物组数据，有 也在疾病和健康样本中收集。充分了解人类疾病的复杂基础 和正常的表型变异，所有这些因素都应该在一个统一的分析中适当地考虑 框架，以及关于环境暴露和其他风险因素的流行病学数据。讨论 如何应对这些数据来源带来的分析挑战，我们制定了一项年度 在费城举行的宾夕法尼亚大学校园研讨会，名为 基因组学、流行病学和统计学进展(SAGE)。我们的目标是促进 在基因组学和相关领域弥合新兴技术和数据分析之间差距的分析方法 鼓励方法学科学家和应用科学家之间的交流与合作；并促进 培训年轻调查人员，让尽可能多的人参加我们的会议并促进 他们的积极参与和与较资深参与者的互动。圣人已连续举行 自2013年以来，参与者数量不断增加，参与者满意度也不断提高，达到98.9% 对研讨会后调查的答复者强烈同意或同意这样的声明：“我很高兴参加 《智者2018》。我们建议在2019年和2020年继续这一成功的模式。每年我们都会选择主题 在与基因组学和其他高维度数据有关的统计和流行病学方法领域 关于感知的兴趣和对研究的潜在影响。我们将邀请从专家中选出的7位演讲者 在美国的机构中，包括理论和应用科学家。参与者将被邀请提交一份 摘要与他们的注册，和两个海报会议将允许他们介绍自己的当前研究。 两篇由学生或博士后提交的摘要将被选作口头报告。座谈会前的一次“会议” 演讲者为初级参与者举行的聚会和对所有参与者开放的最终招待会将鼓励 非正式互动，目的是促进合作和确定可能的新导师-受训者 两性关系。超过78%的研讨会后调查受访者强烈同意或同意 声明“我通过参加对我的工作有价值的2018年圣人会议与同事们建立了联系”。我们的 最终目标是促进培训、协作以及方法的开发和应用 进一步加深我们对导致人类疾病的复杂机制的理解。

Abstract Advances in technology and significant decrease in costs are driving progress in genomic studies. Studies of whole exome and genome sequences of complex traits in large samples are increasingly common. Other sources of high-dimensional information, including expression, epigenetic, metabolic and microbiome data, are also being collected in disease and healthy samples. To fully understand the complex bases of human disease and normal phenotypic variability, all of these factors should be properly considered in a unified analytical framework, together with epidemiological data on environmental exposures and other risk factors. To discuss how to address the analytical challenges presented by these sources of data, we have developed an annual symposium held in Philadelphia on the campus of the University of Pennsylvania, named Symposium on Advances in Genomics, Epidemiology, and Statistics (SAGES). Our objectives are to favor development of analytical methods to bridge the gap between emerging technologies and data analysis in genomics and related fields; to encourage exchange and collaboration between methodological and applied scientists; and to foster training of young investigators by giving access to our conference to the largest possible number and promoting their active participation and interaction with the more senior participants. SAGES has been held continuously since 2013 and has enjoyed an increasing number of participants as well as participant satisfaction, with 98.9% of respondent to the post-symposium survey strongly agreeing or agreeing to the statement “I enjoyed attending SAGES 2018”. We propose to continue this successful formula in 2019 and 2020. Each year we will select topics in the area of statistical and epidemiological methods related to genomics and other high-dimensional data based on perceived interest and potential impact on research. We will invite 7 speakers chosen among experts working in US institutions, including both theoretical and applied scientists. Participants will be invited to submit an abstract with their registration, and two poster sessions will allow them to present their own current research. Two abstracts presented by students or post-docs will be selected for oral presentation. A pre-symposium “Meet the Speakers” get-together for junior attendees and a final reception open to all participants will encourage informal interactions, with the goal of facilitating collaborations and identification of possible new mentor-trainee relationships. More than 78% of respondent to the post-symposium survey strongly agreed or agreed with the statement “I made connections with colleagues by attending SAGES 2018 that are valuable for my work”. Our final goal is to promote training, collaboration, and the development and application of methodologies that will further our understanding of the complex mechanisms responsible for human disorders.