Critical points for an accurate human genome analysis-Reference-Cited by-同舟云学术

Critical points for an accurate human genome analysis

Published:2017-06-16 Issue:8 Volume:38 Page:912-921
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

White Stefan J.¹^ORCID,Laros Jeroen F.J.¹²³,Bakker Egbert²,Cambon‐Thomsen Anne⁴,Eden Martin⁵,Leonard Samantha⁴,Lochmüller Hanns⁶,Matthijs Gert⁷,Mattocks Christopher⁸,Patton Simon⁹,Payne Katherine⁵,Scheffer Hans¹⁰,Souche Erica⁷,Thomassen Ellen¹,Thompson Rachel⁶,Traeger‐Synodinos Jan¹¹,Vooren Steven¹²,Janssen Bart³,den Dunnen Johan T.¹²^ORCID

Affiliation:

1. Department of Human Genetics, Leiden University Medical Center The Netherlands

2. Clinical GeneticsLeiden University Medical Center The Netherlands

3. GenomeScan Leiden The Netherlands

4. Epidemiology and Public Health Analyses, Inserm and Université Toulouse III Paul Sabatier Toulouse UMR 1027 France

5. Manchester Centre for Health Economics, University of Manchester Manchester UK

6. Institute of Genetic Medicine, Newcastle University Newcastle upon Tyne UK

7. Catholic University Leuven Leuven Belgium

8. Wessex Regional Genetic Laboratory Salisbury UK

9. Central Manchester University Hospitals Foundation Trust, EMQN Manchester UK

10. UMC St. Radboud, Nijmegen The Netherlands

11. Medical GeneticsNational and Kapodistrian University of Athens Greece

12. Agilent Technologies Lexington Massachusetts

Funder

Seventh Framework Programme

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.23238

Reference88 articles.

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4. Cell line misidentification: the beginning of the end

5. Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants

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