Literature DB >> 33726816

Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients.

Henrik Stranneheim1,2,3, Kristina Lagerstedt-Robinson1,4, Anna Lindstrand5,6, Anna Wedell7,8,9, Måns Magnusson1,3, Malin Kvarnung1,4, Daniel Nilsson1,4, Nicole Lesko1,2, Martin Engvall1,2, Britt-Marie Anderlid1,4, Henrik Arnell10, Carolina Backman Johansson2, Michela Barbaro2, Erik Björck1,4, Helene Bruhn2,11, Jesper Eisfeldt1,4, Christoph Freyer2,11, Giedre Grigelioniene1,4, Peter Gustavsson1,4, Anna Hammarsjö1,4, Maritta Hellström-Pigg1,4, Erik Iwarsson1,4, Anders Jemt1, Mikael Laaksonen12, Sara Lind Enoksson13, Helena Malmgren1,4, Karin Naess2, Magnus Nordenskjöld1,4, Mikael Oscarson2, Maria Pettersson1,4, Chiara Rasi3, Adam Rosenbaum12, Ellika Sahlin1,4, Eliane Sardh1,2, Tommy Stödberg2,10, Bianca Tesi1,4, Emma Tham1,4, Håkan Thonberg1,4, Virpi Töhönen1, Ulrika von Döbeln2, Daphne Vassiliou1,2, Sofie Vonlanthen13, Ann-Charlotte Wikström13, Josephine Wincent1,4, Ola Winqvist13, Anna Wredenberg2,11, Sofia Ygberg2,10, Rolf H Zetterström1,2, Per Marits13, Maria Johansson Soller1,4, Ann Nordgren1,4, Valtteri Wirta3,12.   

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.

Entities:  

Keywords:  Clinical diagnostics; Monogenic disease; Single nucleotide variant; Whole genome sequencing

Mesh:

Year:  2021        PMID: 33726816      PMCID: PMC7968334          DOI: 10.1186/s13073-021-00855-5

Source DB:  PubMed          Journal:  Genome Med        ISSN: 1756-994X            Impact factor:   11.117


  45 in total

1.  Deep sequencing of 10,000 human genomes.

Authors:  Amalio Telenti; Levi C T Pierce; William H Biggs; Julia di Iulio; Emily H M Wong; Martin M Fabani; Ewen F Kirkness; Ahmed Moustafa; Naisha Shah; Chao Xie; Suzanne C Brewerton; Nadeem Bulsara; Chad Garner; Gary Metzker; Efren Sandoval; Brad A Perkins; Franz J Och; Yaron Turpaz; J Craig Venter
Journal:  Proc Natl Acad Sci U S A       Date:  2016-10-04       Impact factor: 11.205

2.  Adenosine kinase deficiency disrupts the methionine cycle and causes hypermethioninemia, encephalopathy, and abnormal liver function.

Authors:  Magnus K Bjursell; Henk J Blom; Jordi Asin Cayuela; Martin L Engvall; Nicole Lesko; Shanti Balasubramaniam; Göran Brandberg; Maria Halldin; Maria Falkenberg; Cornelis Jakobs; Desiree Smith; Eduard Struys; Ulrika von Döbeln; Claes M Gustafsson; Joakim Lundeberg; Anna Wedell
Journal:  Am J Hum Genet       Date:  2011-09-28       Impact factor: 11.025

3.  Whole-genome sequencing of patients with rare diseases in a national health system.

Authors:  Ernest Turro; William J Astle; Karyn Megy; Stefan Gräf; Daniel Greene; Olga Shamardina; Hana Lango Allen; Alba Sanchis-Juan; Mattia Frontini; Chantal Thys; Jonathan Stephens; Rutendo Mapeta; Oliver S Burren; Kate Downes; Matthias Haimel; Salih Tuna; Sri V V Deevi; Timothy J Aitman; David L Bennett; Paul Calleja; Keren Carss; Mark J Caulfield; Patrick F Chinnery; Peter H Dixon; Daniel P Gale; Roger James; Ania Koziell; Michael A Laffan; Adam P Levine; Eamonn R Maher; Hugh S Markus; Joannella Morales; Nicholas W Morrell; Andrew D Mumford; Elizabeth Ormondroyd; Stuart Rankin; Augusto Rendon; Sylvia Richardson; Irene Roberts; Noemi B A Roy; Moin A Saleem; Kenneth G C Smith; Hannah Stark; Rhea Y Y Tan; Andreas C Themistocleous; Adrian J Thrasher; Hugh Watkins; Andrew R Webster; Martin R Wilkins; Catherine Williamson; James Whitworth; Sean Humphray; David R Bentley; Nathalie Kingston; Neil Walker; John R Bradley; Sofie Ashford; Christopher J Penkett; Kathleen Freson; Kathleen E Stirrups; F Lucy Raymond; Willem H Ouwehand
Journal:  Nature       Date:  2020-06-24       Impact factor: 49.962

4.  Second-generation PLINK: rising to the challenge of larger and richer datasets.

Authors:  Christopher C Chang; Carson C Chow; Laurent Cam Tellier; Shashaank Vattikuti; Shaun M Purcell; James J Lee
Journal:  Gigascience       Date:  2015-02-25       Impact factor: 6.524

5.  Identification of three novel FGF16 mutations in X-linked recessive fusion of the fourth and fifth metacarpals and possible correlation with heart disease.

Authors:  Tobias Laurell; Daniel Nilsson; Wolfgang Hofmeister; Anna Lindstrand; Nadav Ahituv; Julia Vandermeer; Anders Amilon; Göran Annerén; Marianne Arner; Maria Pettersson; Nina Jäntti; Hans-Eric Rosberg; Peter A Cattini; Agneta Nordenskjöld; Outi Mäkitie; Giedre Grigelioniene; Ann Nordgren
Journal:  Mol Genet Genomic Med       Date:  2014-05-14       Impact factor: 2.183

6.  Who's Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with Peddy.

Authors:  Brent S Pedersen; Aaron R Quinlan
Journal:  Am J Hum Genet       Date:  2017-02-09       Impact factor: 11.025

7.  From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability.

Authors:  Anna Lindstrand; Jesper Eisfeldt; Maria Pettersson; Claudia M B Carvalho; Malin Kvarnung; Giedre Grigelioniene; Britt-Marie Anderlid; Olof Bjerin; Peter Gustavsson; Anna Hammarsjö; Patrik Georgii-Hemming; Erik Iwarsson; Maria Johansson-Soller; Kristina Lagerstedt-Robinson; Agne Lieden; Måns Magnusson; Marcel Martin; Helena Malmgren; Magnus Nordenskjöld; Ameli Norling; Ellika Sahlin; Henrik Stranneheim; Emma Tham; Josephine Wincent; Sofia Ygberg; Anna Wedell; Valtteri Wirta; Ann Nordgren; Johanna Lundin; Daniel Nilsson
Journal:  Genome Med       Date:  2019-11-07       Impact factor: 11.117

8.  Absence of GP130 cytokine receptor signaling causes extended Stüve-Wiedemann syndrome.

Authors:  Yin-Huai Chen; Giedre Grigelioniene; Phillip T Newton; Jacob Gullander; Maria Elfving; Anna Hammarsjö; Dominyka Batkovskyte; Hessa S Alsaif; Wesam I Y Kurdi; Firdous Abdulwahab; Veerabahu Shanmugasundaram; Luke Devey; Séverine Bacrot; Jana Brodszki; Celine Huber; Ben Hamel; David Gisselsson; Nikos Papadogiannakis; Katarina Jedrycha; Barbara Gürtl-Lackner; Andrei S Chagin; Gen Nishimura; Dominik Aschenbrenner; Fowzan S Alkuraya; Arian Laurence; Valérie Cormier-Daire; Holm H Uhlig
Journal:  J Exp Med       Date:  2020-03-02       Impact factor: 14.307

9.  Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26.

Authors:  Yoshihito Kishita; Aleksandra Pajak; Nikhita Ajit Bolar; Carlo M T Marobbio; Camilla Maffezzini; Daniela V Miniero; Magnus Monné; Masakazu Kohda; Henrik Stranneheim; Kei Murayama; Karin Naess; Nicole Lesko; Helene Bruhn; Arnaud Mourier; Rolf Wibom; Inger Nennesmo; Ann Jespers; Paul Govaert; Akira Ohtake; Lut Van Laer; Bart L Loeys; Christoph Freyer; Ferdinando Palmieri; Anna Wredenberg; Yasushi Okazaki; Anna Wedell
Journal:  Am J Hum Genet       Date:  2015-10-29       Impact factor: 11.025

10.  Gain-of-function mutation of microRNA-140 in human skeletal dysplasia.

Authors:  Giedre Grigelioniene; Hiroshi I Suzuki; Fulya Taylan; Fatemeh Mirzamohammadi; Zvi U Borochowitz; Ugur M Ayturk; Shay Tzur; Eva Horemuzova; Anna Lindstrand; Mary Ann Weis; Gintautas Grigelionis; Anna Hammarsjö; Elin Marsk; Ann Nordgren; Magnus Nordenskjöld; David R Eyre; Matthew L Warman; Gen Nishimura; Phillip A Sharp; Tatsuya Kobayashi
Journal:  Nat Med       Date:  2019-02-25       Impact factor: 53.440

View more
  21 in total

Review 1.  Monogenic inflammatory bowel disease-genetic variants, functional mechanisms and personalised medicine in clinical practice.

Authors:  Aline Azabdaftari; Kelsey D J Jones; Jochen Kammermeier; Holm H Uhlig
Journal:  Hum Genet       Date:  2022-06-28       Impact factor: 4.132

2.  Patient-Specific Assays Based on Whole-Genome Sequencing Data to Measure Residual Disease in Children With Acute Lymphoblastic Leukemia: A Proof of Concept Study.

Authors:  Cecilia Arthur; Fatemah Rezayee; Nina Mogensen; Leonie Saft; Richard Rosenquist; Magnus Nordenskjöld; Arja Harila-Saari; Emma Tham; Gisela Barbany
Journal:  Front Oncol       Date:  2022-07-05       Impact factor: 5.738

3.  Case Report: Inversion of LMX1B - A Novel Cause of Nail-Patella Syndrome in a Swedish Family and a Longtime Follow-Up.

Authors:  Hillevi Lindelöf; Eva Horemuzova; Ulrika Voss; Ann Nordgren; Giedre Grigelioniene; Anna Hammarsjö
Journal:  Front Endocrinol (Lausanne)       Date:  2022-06-13       Impact factor: 6.055

4.  Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG).

Authors:  Kandamurugu Manickam; Monica R McClain; Laurie A Demmer; Sawona Biswas; Hutton M Kearney; Jennifer Malinowski; Lauren J Massingham; Danny Miller; Timothy W Yu; Fuki M Hisama
Journal:  Genet Med       Date:  2021-07-01       Impact factor: 8.822

Review 5.  Whole-genome sequencing as a first-tier diagnostic framework for rare genetic diseases.

Authors:  Haseeb Nisar; Bilal Wajid; Samiah Shahid; Faria Anwar; Imran Wajid; Asia Khatoon; Mian Usman Sattar; Saima Sadaf
Journal:  Exp Biol Med (Maywood)       Date:  2021-09-15

6.  The impact of genomics on precision public health: beyond the pandemic.

Authors:  Muin J Khoury; Kathryn E Holt
Journal:  Genome Med       Date:  2021-04-23       Impact factor: 11.117

7.  Novel Mutation of the TGF-β 3 Protein (Loeys-Dietz Type 5) Associated With Aortic and Carotid Dissections: Case Report.

Authors:  Dargham Hussein; Christian Olsson; Kristina Lagerstedt-Robinson; Tiago Moreira
Journal:  Neurol Genet       Date:  2021-09-14

8.  Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study.

Authors:  Katherine R Schon; Rita Horvath; Wei Wei; Claudia Calabrese; Arianna Tucci; Kristina Ibañez; Thiloka Ratnaike; Robert D S Pitceathly; Enrico Bugiardini; Rosaline Quinlivan; Michael G Hanna; Emma Clement; Emma Ashton; John A Sayer; Paul Brennan; Dragana Josifova; Louise Izatt; Carl Fratter; Victoria Nesbitt; Timothy Barrett; Dominic J McMullen; Audrey Smith; Charulata Deshpande; Sarah F Smithson; Richard Festenstein; Natalie Canham; Mark Caulfield; Henry Houlden; Shamima Rahman; Patrick F Chinnery
Journal:  BMJ       Date:  2021-11-03

9.  A retrospective two centre study of Birt-Hogg-Dubé syndrome reveals a pathogenic founder mutation in FLCN in the Swedish population.

Authors:  Kristina Lagerstedt-Robinson; Izabella Baranowska Körberg; Stefanos Tsiaprazis; Erik Björck; Emma Tham; Anna Poluha; Maritta Hellström Pigg; Ylva Paulsson-Karlsson; Magnus Nordenskjöld; Maria Johansson-Soller; Christos Aravidis
Journal:  PLoS One       Date:  2022-02-17       Impact factor: 3.240

10.  De Novo ACTG1 Variant Expands the Phenotype and Genotype of Partial Deafness and Baraitser-Winter Syndrome.

Authors:  Mateusz Dawidziuk; Anna Kutkowska-Kazmierczak; Ewelina Bukowska-Olech; Marta Jurek; Ewa Kalka; Dorothy Lys Guilbride; Mariusz Ireneusz Furmanek; Monika Bekiesinska-Figatowska; Jerzy Bal; Pawel Gawlinski
Journal:  Int J Mol Sci       Date:  2022-01-08       Impact factor: 5.923

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.