13:30 AI-driven rare disease phenotype representation with application to diagnostics Michael Yates ( University of Edinburgh) 13:40 An Audit for Whole Genome Sequencing of 8000 diagnostic cases as part of the Genomic Medicine Service Gavin Ryan ( Regional Genetics Laboratory, Birmingham) 13:45 Functional genomics supporting diagnosis and therapy in phenylketonuria (PKU) – A national cohort study Rachael E McNeilly (Bristol Genetics Laboratory) 13:50 Biallelic UGGT1 gene variants cause a congenital disorder of glycosylation Laura Harrold (University of Exeter Medical School) 14:00 Leveraging natural language processing for a service improvement model in familial thoracic aortic aneurysm Alexander Deng (Guy's and St Thomas's NHS Foundation Trust) 14:05 Keeping up with新的基因发现:一种简单的计算方法,用于重新分析基因组数据fiona Price-kuehne(伦敦大学儿童健康研究所)14:10阐明了肌醇多磷酸磷酸磷酸磷酸酶磷酸磷酸酶Inpp4a inpp4a ppp4a相关的神经发育疾病的临床和遗传谱,并测试了exeter(exeter of Exeter of Exeter)14:15 Irlord:14:15 irliand:14:15通过基因测试视频(Genvid)研究:革命或进化,促进及时且公平的Emma Baple(ACGS稀有疾病位置陈述工作组)14:40对遗传性心脏条件的新基因测试途径的评估:一场革命或进化?一项多站点调查研究RIA Patel(伦敦大学医学院)Lisa Bryson (West of Scotland Clinical Genetics Service, Glasgow) 14:45 UK population primary care electronic health record databases are valuable but underutilised resources for studying rare genetic conditions Thomas Wright (Manchester University NHS Foundation Trust) 14:50 Are we effectively supporting parents making decisions about whole genome sequencing in the Genomic Medicine Service?
市场上有大量基于光学技术的区域表面形貌测量仪器。然而,由于缺乏对光与元件表面之间复杂相互作用的理解,将光学仪器投入生产存在问题 - 研究仪器的光学传递函数可以帮助解决这个问题。本报告的目的是回顾光学传递函数测量技术。从空间相干单色共焦扫描成像系统的基础出发,介绍了三维 (3D) 成像中的光学传递函数理论。进一步的概括被回顾,允许将该理论扩展到描述传统和干涉 3D 成像系统,在一系列空间相干性上。还简要考虑了多色传递函数。进一步专门研究表面形貌的测量。在介绍理论结果之后,介绍了测量每类系统光学传递函数的实验方法,重点介绍了在 3D 成像和表面形貌测量中建立校准标准的合适方法。