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Detection of Rare Mutations in CtDNA Using Next Generation Sequencing
Published on: August 24, 2017
[Application of Next-Generation Sequencing in Rare Renal Diseases]
1Department of Nephrology,Affiliated Hospital of Inner Mongolia Medical University,Hohhot 010000,China.
Abstract:
Rare diseases refer to the diseases with low prevalence,among which more than 150 kinds involve the kidney.Most of the rare renal diseases have genetic background.Due to complex etiology and diverse clinical phenotypes,most patients have progressed to the final stage of the disease before a clear diagnosis.Gene testing is a powerful tool for the diagnosis of rare renal diseases.The emergence of the next-generation sequencing (NGS) significantly improves the diagnostic efficiency and quality and provides an unprecedented opportunity to understand the molecular genetic basis of rare renal diseases and further select or develop targeted therapies.This article reviews the application progress,challenges,and prospects of NGS in rare kidney diseases.

