Targeted Next-Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics-Reference-Cited by-同舟云学术

Targeted Next-Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics

Published:2013-04-29 Issue:7 Volume:34 Page:1035-1042
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Sikkema-Raddatz Birgit¹,Johansson Lennart F.¹,de Boer Eddy N.¹,Almomani Rowida¹,Boven Ludolf G.¹,van den Berg Maarten P.²,van Spaendonck-Zwarts Karin Y.¹,van Tintelen J. Peter¹,Sijmons Rolf H.¹,Jongbloed Jan D. H.¹,Sinke Richard J.¹

Affiliation:

1. Department of Genetics; University of Groningen; University Medical Centre Groningen; Groningen The Netherlands

2. Department of Cardiology; University of Groningen; University Medical Centre Groningen; Groningen The Netherlands

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.22332/fullpdf

Reference20 articles.

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4. Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome;Gilissen;Am J Hum Genet,2010

5. Disease gene identification strategies for exome sequencing;Gilissen;Eur J Hum Genet,2012

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