1. Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients
- Author
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Tommy Stödberg, Magnus Nordenskjöld, Emma Tham, Virpi Töhönen, Karin Naess, Bianca Tesi, Eliane Sardh, Erik Björck, Martin Engvall, Helena Malmgren, Josephine Wincent, Adam Rosenbaum, Peter Gustavsson, Sofie Vonlanthen, Anders Jemt, Måns Magnusson, Helene Bruhn, Anna Wredenberg, Mikael Oscarson, Sofia Ygberg, Kristina Lagerstedt-Robinson, Erik Iwarsson, Carolina Backman Johansson, Christoph Freyer, Michela Barbaro, Ellika Sahlin, Henrik Stranneheim, Anna Lindstrand, Anna Wedell, Ann Nordgren, Ulrika von Döbeln, Britt-Marie Anderlid, Mikael Laaksonen, Maria Pettersson, Henrik Arnell, Nicole Lesko, Rolf Zetterström, Chiara Rasi, Ann-Charlotte Wikström, Malin Kvarnung, Valtteri Wirta, Sara Lind Enoksson, Giedre Grigelioniene, Maria Johansson Soller, Anna Hammarsjö, Ola Winqvist, Daphne Vassiliou, Håkan Thonberg, Per Marits, Jesper Eisfeldt, Daniel Nilsson, and Maritta Hellström-Pigg
- Subjects
medicine.medical_specialty ,lcsh:QH426-470 ,DNA Copy Number Variations ,Inheritance Patterns ,lcsh:Medicine ,Genomics ,Disease ,Cohort Studies ,Genetic Heterogeneity ,Rare Diseases ,Internal medicine ,Genetics ,medicine ,Humans ,Medical diagnosis ,Indel ,Monogenic disease ,Molecular Biology ,Genetics (clinical) ,Whole genome sequencing ,Sweden ,Whole Genome Sequencing ,business.industry ,Information Dissemination ,Research ,lcsh:R ,High-Throughput Nucleotide Sequencing ,Uniparental Disomy ,medicine.disease ,Human genetics ,Uniparental disomy ,Single nucleotide variant ,lcsh:Genetics ,Clinical diagnostics ,Mutation ,Molecular Medicine ,business ,Delivery of Health Care ,Rare disease ,Microsatellite Repeats - Abstract
Background We report the findings from 4437 individuals (3219 patients and 1218 relatives) who have been analyzed by whole genome sequencing (WGS) at the Genomic Medicine Center Karolinska-Rare Diseases (GMCK-RD) since mid-2015. GMCK-RD represents a long-term collaborative initiative between Karolinska University Hospital and Science for Life Laboratory to establish advanced, genomics-based diagnostics in the Stockholm healthcare setting. Methods Our analysis covers detection and interpretation of SNVs, INDELs, uniparental disomy, CNVs, balanced structural variants, and short tandem repeat expansions. Visualization of results for clinical interpretation is carried out in Scout—a custom-developed decision support system. Results from both singleton (84%) and trio/family (16%) analyses are reported. Variant interpretation is done by 15 expert teams at the hospital involving staff from three clinics. For patients with complex phenotypes, data is shared between the teams. Results Overall, 40% of the patients received a molecular diagnosis ranging from 19 to 54% for specific disease groups. There was heterogeneity regarding causative genes (n = 754) with some of the most common ones being COL2A1 (n = 12; skeletal dysplasia), SCN1A (n = 8; epilepsy), and TNFRSF13B (n = 4; inborn errors of immunity). Some causative variants were recurrent, including previously known founder mutations, some novel mutations, and recurrent de novo mutations. Overall, GMCK-RD has resulted in a large number of patients receiving specific molecular diagnoses. Furthermore, negative cases have been included in research studies that have resulted in the discovery of 17 published, novel disease-causing genes. To facilitate the discovery of new disease genes, GMCK-RD has joined international data sharing initiatives, including ClinVar, UDNI, Beacon, and MatchMaker Exchange. Conclusions Clinical WGS at GMCK-RD has provided molecular diagnoses to over 1200 individuals with a broad range of rare diseases. Consolidation and spread of this clinical-academic partnership will enable large-scale national collaboration.
- Published
- 2021