The Authors identified by Illuminabased exome

The Authors identified by Illuminabased exome sequencing allelic ISPD variants in nine cases belonging to seven families. The same ISPD gene and the TMEM5 gene have been previously identified as the genetic causes of the Cobblestone lissencephaly (27). Diagnosis of genetic muscle disorders by NGS The use of targeted NGS for clinical diagnostics should be considered as a cost-effective Inhibitors,research,lifescience,medical alternative, when the total number of PCR fragments of the candidate genes exceeds the 96 wells of a PCR plate used to perform Sanger sequencing reactions. All the different disorders of muscle present diagnostic challenges due to phenotypic

variability, and difficulties with muscle immunohistochemical studies (28-31). The dystrophin gene has been the first challenge for targeted NGS by our group (32) and http://www.selleckchem.com/products/lapatinib.html recently, by others (33). This is Inhibitors,research,lifescience,medical because the Dystrophin (DMD) gene is large and the spectrum of point mutations is unpredictable. However, the muscle cDNA Inhibitors,research,lifescience,medical Sanger sequencing in DMD cases remains the more convenient option, because any targeting method can miss some sequences. Valencia et al. (34) used NGS to identify mutations in 321 exons representing 12 different genes involved with congenital muscular dystrophies. Two different enrichment technologies were used, solution-based hybridization and microdroplet-based

PCR target enrichment. Inhibitors,research,lifescience,medical NGS results were analyzed and compared with Sanger sequencing. Both enrichment technologies produced suitable data for clinical laboratories. In a recent study, 267 neuromuscular disease genes

were targeted by affinity capture for enrichment and eight patients were studied (35). With this protocol more than 97% of the targeted exons were fully covered. However, clinical labs are fast moving towards the routine use of whole exome sequencing. The exome sequencing has been also applied to the diagnosis of known conditions, such as a case of autosomal recessive Emery- Inhibitors,research,lifescience,medical Dreifuss muscular dystrophy caused by a novel homozygous mutation (R225Q) in the lamin A/C gene (36). Another successful use of whole exome sequencing was the identification of the cause Batimastat of autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy (ARVC) in a Swedish family. A heterozygous mutation was identified that replaces p.Pro419Ser in the desmin gene on chromosome 2q35 (37). Whole exome sequencing was also used to diagnose a LGMD2A, erroneously assigned as selleck non-4q FSHD (FSHD2). This also shows how wrong diagnoses can be corrected by NGS (38). Perspectives This huge potential of the next generation sequencing applications makes likely that these will soon become the first approach in clinical laboratories.

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