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The Changing Landscape of Molecular Diagnostic Testing: Implications for Academic Medical Centers

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Journal J Pers Med
Date 2016 Feb 2
PMID 26828522
Citations 10
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Abstract

Over the last decade, the field of molecular diagnostics has undergone tremendous transformation, catalyzed by the clinical implementation of next generation sequencing (NGS). As technical capabilities are enhanced and current limitations are addressed, NGS is increasingly capable of detecting most variant types and will therefore continue to consolidate and simplify diagnostic testing. It is likely that genome sequencing will eventually serve as a universal first line test for disorders with a suspected genetic origin. Academic Medical Centers (AMCs), which have been at the forefront of this paradigm shift are now presented with challenges to keep up with increasing technical, bioinformatic and interpretive complexity of NGS-based tests in a highly competitive market. Additional complexity may arise from altered regulatory oversight, also triggered by the unprecedented scope of NGS-based testing, which requires new approaches. However, these challenges are balanced by unique opportunities, particularly at the interface between clinical and research operations, where AMCs can capitalize on access to cutting edge research environments and establish collaborations to facilitate rapid diagnostic innovation. This article reviews present and future challenges and opportunities for AMC associated molecular diagnostic laboratories from the perspective of the Partners HealthCare Laboratory for Molecular Medicine (LMM).

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References
1.
Neveling K, Feenstra I, Gilissen C, Hoefsloot L, Kamsteeg E, Mensenkamp A . A post-hoc comparison of the utility of sanger sequencing and exome sequencing for the diagnosis of heterogeneous diseases. Hum Mutat. 2013; 34(12):1721-6. DOI: 10.1002/humu.22450. View

2.
Xue Y, Ankala A, Wilcox W, Hegde M . Solving the molecular diagnostic testing conundrum for Mendelian disorders in the era of next-generation sequencing: single-gene, gene panel, or exome/genome sequencing. Genet Med. 2014; 17(6):444-51. DOI: 10.1038/gim.2014.122. View

3.
Richards J, Korgenski E, Srivastava R, Bonkowsky J . Costs of the diagnostic odyssey in children with inherited leukodystrophies. Neurology. 2015; 85(13):1167-70. PMC: 4603881. DOI: 10.1212/WNL.0000000000001974. View

4.
Rehm H . Disease-targeted sequencing: a cornerstone in the clinic. Nat Rev Genet. 2013; 14(4):295-300. PMC: 3786217. DOI: 10.1038/nrg3463. View

5.
Gowrisankar S, Lerner-Ellis J, Cox S, White E, Manion M, LeVan K . Evaluation of second-generation sequencing of 19 dilated cardiomyopathy genes for clinical applications. J Mol Diagn. 2010; 12(6):818-27. PMC: 2963910. DOI: 10.2353/jmoldx.2010.100014. View