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Targeted capture and massively parallel sequencing in pediatric cardiomyopathy: development of novel diagnostics

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Author(s): Muhammad Tariq | Thanh-Tam Le | Patrick Putnam | Steven Kindel | Mehdi Keddache | Stephanie M. Ware

Journal: Cardiogenetics
ISSN 2035-8253

Volume: 2;
Issue: 1;
Date: 2012;
Original page

Keywords: sequence capture | massively parallel sequencing | restrictive cardiomyopathy | desmin | missense mutation.

ABSTRACT
Pediatric cardiomyopathy is a genetically heterogeneous disease associated with significant morbidity. Although identification of underlying etiology is important for management, therapy, and screening at risk family members, molecular diagnosis is difficult due to the large number of causative genes, high rate of private mutations, and cost. We aimed to define the genetic basis of pediatric cardiomyopathy and test a novel diagnostic tool using a custom targeted microarray coupled to massively parallel sequencing. Three patients with cardiomyopathy were screened using a custom NimbleGen sequence capture array containing 110 genes and providing 99.9% coverage of the exons of interest. The sensitivity and specificity was >99% as determined by comparison to long range PCR-based massively parallel sequencing, Sanger sequencing of missense variants, and SNP genotyping using the Illumina Infinium Omni1 array. Overall, 99.73% of the targeted regions were captured and sequenced at >10X coverage, allowing reliable mutation calling in all patients. Analysis identified a total of 165 non-synonymous coding single nucleotide polymorphisms (cSNPs), of which 89 were unique and 14 were novel. On average, each patient had 4 cSNPs predicted to be pathogenic. We report a cardiomyopathy sequencing array that allows simultaneous assessment of 110 genes. Comparison of targeted sequence capture vs. PCR-based enrichment methods demonstrates that the former is more sensitive and efficient. Array-based sequence capture technology followed by massively parallel sequencing is promising as a robust and comprehensive tool for genetic screening of cardiomyopathy. These results provide important information about genetic architecture and indicate that improved annotation of variants and interpretation of clinical significance, particularly in cases with multiple rare variants, are important for clinical utility.
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