Fast and robust next-generation sequencing technique using ion torrent personal genome machine for the screening of neurofibromatosis type 1 (NF1) gene

Bernadett Balla, Kristóf Árvai, Péter Horváth, Bálint Tobiás, István Takács, Zsolt Nagy, Magdolna Dank, György Fekete, János P. Kósa, Péter Lakatos

Research output: Article

16 Citations (Scopus)

Abstract

Neurofibromatosis type 1 (NF1) gene exhibits one of the highest spontaneous mutation rates in the human genome. Identification of the NF1 mutation is challenging because the NF1 gene is very large and complex, lacking mutational "hot spots." There is no clustering of mutations, there are several pseudogenes, and a wide spectrum of different types of mutation has been recognized. To date, NF1 mutations or deleted regions have been detected with a number of techniques. With the appearance of next-generation sequencing (NGS) machines, molecular biology is in a new revolutionary phase. Our aim was to work out a method to use the high-throughput NGS machine, Ion Torrent PGM, in diagnostic settings for neurofibromatosis type 1. In our examination, we could reveal 21 distinct variations in NF1 gene in seven patients. This is an absolutely new method for exploring the genetic background of neurofibromatosis type 1 exhibiting the extremely high throughput of NGS in a diagnostic setting.

Original languageEnglish
Pages (from-to)204-210
Number of pages7
JournalJournal of Molecular Neuroscience
Volume53
Issue number2
DOIs
Publication statusPublished - jún. 2014

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience

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