Guidelines for diagnostic next-generation sequencing

被引:353
|
作者
Matthijs, Gert [1 ]
Souche, Erika [1 ]
Alders, Marielle [2 ]
Corveleyn, Anniek [1 ]
Eck, Sebastian [3 ]
Feenstra, Ilse [4 ]
Race, Valerie [1 ]
Sistermans, Erik [5 ]
Sturm, Marc [6 ]
Weiss, Marjan [5 ]
Yntema, Helger [4 ]
Bakker, Egbert [7 ]
Scheffer, Hans [4 ]
Bauer, Peter [6 ]
机构
[1] Katholieke Univ Leuven, Ctr Human Genet, Lab Mol Diag, B-3000 Leuven, Belgium
[2] Univ Amsterdam, Acad Med Ctr, Dept Clin Genet, NL-1105 AZ Amsterdam, Netherlands
[3] Ctr Human Genet & Lab Med, Martinsried, Germany
[4] Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands
[5] Vrije Univ Amsterdam, Med Ctr, Dept Clin Genet, Amsterdam, Netherlands
[6] Univ Tubingen Hosp, Inst Med Genet & Appl Genom, Tubingen, Germany
[7] Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, Netherlands
关键词
D O I
10.1038/ejhg.2015.226
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:2 / 5
页数:4
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