Erschienen in:
01.06.2014 | Journal club
Applications of next-generation whole exome sequencing
verfasst von:
Katharine E. Harding, Neil P. Robertson
Erschienen in:
Journal of Neurology
|
Ausgabe 6/2014
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Excerpt
Since the publication of the first human genome in 2001, significant advances in understanding the genetic aetiology of neurological diseases have been made. However, genetic heterogeneity, relative rarity of clinical presentation, and high cost of current genetic sequencing methods have limited identification of causative mutations in many other patients. It is becoming apparent that a range of mutations may cause similar clinical phenotypes, which means that consecutive Sanger sequencing of individual genes is time consuming and very expensive, and still may not provide a final answer. …