@article{73faaf6f8b004ee5a39bd32ba39f5c52,
title = "Guidelines for diagnostic next-generation sequencing",
abstract = "We present, on behalf of EuroGentest and the European Society of Human Genetics, guidelines for the evaluation and validation of next-generation sequencing (NGS) applications for the diagnosis of genetic disorders. The work was performed by a group of laboratory geneticists and bioinformaticians, and discussed with clinical geneticists, industry and patients' representatives, and other stakeholders in the field of human genetics. The statements that were written during the elaboration of the guidelines are presented here. The background document and full guidelines are available as supplementary material. They include many examples to assist the laboratories in the implementation of NGS and accreditation of this service. The work and ideas presented by others in guidelines that have emerged elsewhere in the course of the past few years were also considered and are acknowledged in the full text. Interestingly, a few new insights that have not been cited before have emerged during the preparation of the guidelines. The most important new feature is the presentation of a 'rating system' for NGS-based diagnostic tests. The guidelines and statements have been applauded by the genetic diagnostic community, and thus seem to be valuable for the harmonization and quality assurance of NGS diagnostics in Europe.",
author = "G. Matthijs and E. Souche and M. Alders and A. Corveleyn and S. Eck and I. Feenstra and V. Race and E. Sistermans and M. Sturm and M. Weiss and Yntema, {Helger G.} and E. Bakker and H. Scheffer and Peter Bauer",
note = "M1 - 1 ISI Document Delivery No.: CY7UO Times Cited: 26 Cited Reference Count: 0 Matthijs, Gert Souche, Erika Alders, Marielle Corveleyn, Anniek Eck, Sebastian Feenstra, Ilse Race, Valerie Sistermans, Erik Sturm, Marc Weiss, Marjan Yntema, Helger Bakker, Egbert Scheffer, Hans Bauer, Peter Scheffer, Hans/E-4644-2012; Bakker, Egbert/D-3525-2009 Scheffer, Hans/0000-0002-2986-0915; Bakker, Egbert/0000-0002-2843-7357 EuroGentest project [261469]; EC Seventh Framework Program [FP7 - HEALTH-F4-2010] We thank the participants of the first workshop (in Leuven) who discussed aspects of NGS and diagnostics with the writing group and helped drafting the guidelines: Michael Buckley, Luc Dehaspe, Hanns-Georg Klein, Chris Mattocks, Clemens Muller-Reible, Manfred Stuhrmann-Spangenberg, Carla van El, and Jeroen Van Houdt. We are also grateful to the participants of the third meeting (in Nijmegen) who read and commented the first draft of the guidelines: Sergi Beltran, Anna Benet-Pages, Els Dequeker, Koen Devriendt, Sian Ellard, Dirk Goossens, Tina Hambuch, Hanns-Georg Klein, Hanns Lochmuller, Luca Lovrecic, Ira Lubin, Jacek Majewski, Ales Maver, Cor Oosterwijk, Justin Paschall, Guillaume Smits, Maria Soller, Manfred Stuhrmann-Spangenberg, Jonna Tallila, and Steven Van Vooren. We thank the EuroGentest and ESHG members for providing constructive comments, especially Corinna Alberg, Marc Bartoli, Jill Clayton-Smith, Eric Evans, Svetlana Gorokhova-Devred, Alison Hall, Imran Haque, Peter Kang, Martin Krahn, Mark Kroese, Milan Macek, Maryam Mostafavi, William Newman, Tsviya Olender, Sobia Raza, and Jorge Sequeiros. Finally, we thank Liliane Geyskens, Valerie De Groote, and Daniella Kasteel for organizing the different meetings of the working group and the stakeholder meeting. This work has been supported by the EuroGentest project, grant agreement number 261469, funded by the EC Seventh Framework Program theme FP7 - HEALTH-F4-2010. 26 3 8 NATURE PUBLISHING GROUP LONDON EUR J HUM GENET",
year = "2016",
doi = "10.1038/ejhg.2015.226",
language = "English",
volume = "24",
pages = "2--5",
journal = "European Journal of Human Genetics",
issn = "1018-4813",
publisher = "Nature Publishing Group",
}