Reanalysis of genomic data doubles the diagnostic yield for Welsh patients recruited to the UK 100,000 Genomes Project.

IF 4.6 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jana Jezkova, Martin A McClatchey, Sophie Shaw, Rhys Vaughan, Joseph Halstead, Iris Egner, Sharon D Whatley, Arveen Kamath, Oliver Murch, Vinod Varghese, Rachel Irving, Jennifer F Gardner, Ayesha Ahmed, Ian Tully, Vani Jain, Mark T Rogers, Francis H Sansbury, Angus J Clarke, Caroline Pottinger, Maribel Verdesoto Rodriguez, Johann Te Water Naudé, Aimee Bettridge, Alexandra C Martin-Geary, Nils Wagner, Julien Gagneur, Marcela Votruba, David J Bunyan, Kevin Ashelford, Peter Giles, Hywel J Williams, Sian Morgan, Julian R Sampson, Andrew E Fry
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引用次数: 0

Abstract

The 100,000 Genomes Project (100KGP) undertook genome sequencing of patients with rare diseases and cancer to study the role that genes play in disease, and to integrate genomics into UK healthcare. To contribute to 100KGP, the Wales Genomic Medicine Centre (a partnership between the NHS All Wales Medical Genomics Service (AWMGS), Cardiff University and Genomics England) recruited 438 individuals from 154 families that had been subject to pre-genomic genetic testing without reaching a diagnosis. The majority of probands (64%, 98/154) had neurological or neurodevelopmental phenotypes. Genome sequencing, variant calling, gene-based filtering and variant prioritisation were performed by Genomics England. AWMGS undertook clinical interpretation, validation and reporting of variants. Initial diagnostic yield was 20.8% (32/154) with variants of uncertain significance (VUS) reported for 11 more families. Most of the initial findings (83.7%, 36/43) could have been detected by clinical exome sequencing which was standard of care in Wales at the time. Reanalysis of the 100KGP Wales data using updated variant prioritisation tools, expanded gene lists, re-phenotyping and segregation studies, has increased diagnostic yield to 42.2% (65/154) (an improvement of 103%). RNA analysis was used to clarify the clinical significance of VUS in COQ4, ENPP1, GATAD2B, NCAPD2, and THOC2. These findings demonstrate the clinical utility of genome sequencing, RNA analysis, and periodic reanalysis of genomic data.

对基因组数据的重新分析使英国10万基因组计划招募的威尔士患者的诊断率翻了一番。
100,000基因组计划(100KGP)对罕见疾病和癌症患者进行基因组测序,以研究基因在疾病中的作用,并将基因组学整合到英国医疗保健中。为了对100KGP做出贡献,威尔士基因组医学中心(NHS全威尔士医学基因组学服务(AWMGS)、卡迪夫大学和英格兰基因组学之间的合作伙伴关系)从154个家庭中招募了438名个体,这些家庭接受了基因组前基因测试,但没有得到诊断。大多数先证者(64%,98/154)具有神经或神经发育表型。基因组测序、变异召唤、基于基因的过滤和变异优先排序由Genomics England进行。AWMGS承担了变异的临床解释、验证和报告。初步诊断率为20.8%(32/154),另有11个家庭报告了不确定意义变异(VUS)。大多数初步发现(83.7%,36/43)可以通过临床外显子组测序检测到,这是当时威尔士的标准治疗方法。使用更新的变异优先排序工具、扩展的基因列表、重新分型和分离研究对100KGP威尔士数据进行重新分析,已将诊断率提高到42.2%(65/154)(提高103%)。采用RNA分析阐明VUS在COQ4、ENPP1、GATAD2B、NCAPD2和THOC2中的临床意义。这些发现证明了基因组测序、RNA分析和定期再分析基因组数据的临床应用。
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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来源期刊
European Journal of Human Genetics
European Journal of Human Genetics 生物-生化与分子生物学
CiteScore
9.90
自引率
5.80%
发文量
216
审稿时长
2 months
期刊介绍: The European Journal of Human Genetics is the official journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports and reviews in the rapidly expanding field of human genetics and genomics. It covers molecular, clinical and cytogenetics, interfacing between advanced biomedical research and the clinician, and bridging the great diversity of facilities, resources and viewpoints in the genetics community. Key areas include: -Monogenic and multifactorial disorders -Development and malformation -Hereditary cancer -Medical Genomics -Gene mapping and functional studies -Genotype-phenotype correlations -Genetic variation and genome diversity -Statistical and computational genetics -Bioinformatics -Advances in diagnostics -Therapy and prevention -Animal models -Genetic services -Community genetics
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