Female Reproductive Tissue Mapping Center Coordination Core

总结 女性生殖组织绘图中心协调中心（FR TMC）将负责 FR TMC的总体方向以及工作和其他资源的分配，以及中心 管理、行政、法规遵从性、数据和资源共享以及协调 FR TMC中的组件核心和项目之间的沟通。CC还将促进 与其他TMC和转型技术开发（TTP）、快速技术 集成（RTI）、HuBMAP集成、可视化和集成（HIVE）协作实验室和演示 HuBMAP的项目组成部分。CC中的人员将包括FR TMC指导委员会 （由中心主任、项目负责人和其他合作研究者组成）和项目管理人员 工作人员（项目经理、首席临床研究协调员和行政助理）。的 协调委员会的职责将按五个目标组织：1）行政管理（包括 中心的预算和组织前往年度HuBMAP研究者会议，科学会议， 在加州大学圣地亚哥分校和杰克逊实验室的FR TMC研究中心之间）; 2）项目管理（包括：设置和 跟踪优先级、目标和时间表;制定标准操作程序;跟踪样本， 元数据和数据;协调编写进度报告、摘要和手稿）; 3） 法规遵从性（包括建立和维护机构审查委员会的批准， 材料转让协议、数据使用协议和机密披露协议）; 4） 沟通管理（包括：参与HuBMAP工作组和数据发布小组; 以及安排会议和电话会议、管理议程和保存会议记录）;以及5）数据和 资源共享（包括与发展援助委员会合作，准备数据和元数据，以便转移到艾滋病毒/艾滋病研究中心， 并协调FR TMC实验室之间以及FR TMC与 其他HUBMAP中心。协调中心的架构和运作畅顺，有助我们有效率地收集高质素的资料， 高质量的生物标本，并使用最先进的技术生成广泛的成像和分子分析数据 空间转录组学和蛋白质组学技术。建立详细的标准操作 CC的程序将确保我们结果的严谨性和可重复性。CC还将促进快速 与HIVE、其他HuBMAP中心和更广泛的科学界共享数据和资源。

SUMMARY The Coordination Core for the Female Reproductive Tissue Mapping Center (FR TMC) will be responsible for the overall direction of the FR TMC and allocation of effort and other resources, as well as Center management, administration, regulatory compliance, data and resource sharing, and coordination of communication among the component Cores and Projects in the FR TMC. The CC will also facilitate interactions with the other TMCs and the Transformative Technology Development (TTP), Rapid Technology Integration (RTI), HuBMAP Integration, Visualization, and Integration (HIVE) Collaboratory, and Demonstration Project components of HuBMAP. The personnel in the CC will include the FR TMC Steering Committee (comprised of the Center Director, Project Leads, and other Co-Investigators), and the program management staff (Program Manager, Lead Clinical Research Coordinator, and Administrative Assistant). The responsibilities of the CC will be organized in five Aims: 1) Administration (encompassing management of the Center’s budget and organizing travel to annual HuBMAP investigator meetings, scientific conferences, and between FR TMC sites at UC San Diego and Jackson Labs); 2) Program management (including: setting and tracking priorities, goals, and timelines; developing Standard Operating Procedures; tracking samples, metadata, and data; and coordinating preparation of progress reports, abstracts, and manuscripts); 3) Regulatory compliance (including establishment and maintenance of Institutional Review Board approvals, Material Transfer Agreements, Data Use Agreements, and Confidential Disclosure Agreements); 4) Communication management (including: participation in HuBMAP Working Groups and Data Release Teams; and scheduling meetings and conference calls, managing agendas, and keeping minutes); and 5) Data and resource sharing (including working with the DAC to prepare data and metadata for transfer to the HIVE and for public release, and coordinating transfer of materials among FR TMC labs and between the FR TMC and other HuBMAP centers. The structure and smooth operation of the CC will enable us to efficiently collect high- quality biospecimens and generate a broad array of imaging and molecular profiling data using state-of-the art spatial transcriptomic and proteomic technologies. The establishment of detailed Standard Operating Procedures by the CC will ensure the rigor and reproducibility of our results. The CC will also facilitate rapid data and resource sharing with the HIVE, other HuBMAP Centers, and the broader scientific community.