Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing

Author:

Almomani RowidaORCID,Marchi MargheritaORCID,Sopacua Maurice,Lindsey Patrick,Salvi Erika,Koning Bart deORCID,Santoro Silvia,Magri Stefania,Smeets Hubert J. M.,Martinelli Boneschi Filippo,Malik Rayaz R.,Ziegler Dan,Hoeijmakers Janneke G. J.,Bönhof Gidon,Dib-Hajj Sulayman,Waxman Stephen G.,Merkies Ingemar S. J.,Lauria Giuseppe,Faber Catharina G.ORCID,Gerrits Monique M.,

Funder

FP7 Ideas: European Research Council

EIT Health

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference38 articles.

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2. Targeted Next-Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics;B Sikkema-Raddatz;Hum Mutat,2013

3. Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units.;CJ Saunders;Sci Transl Med.,2012

4. Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families;AM Alazami;Cell Rep,2015

5. Emerging Issues in Public Health Genomics.;JS Roberts;Annu Rev Genomics Hum Genet,2014

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