QR Kod

Applying next generation sequencing with microdroplet PCR to determine the disease-causing mutations in retinal dystrophies

Abstract Background Inherited Retinal dystrophy (IRD) is a broad group of inherited retinal disorders with heterogeneous genotypes and phenotypes. Next generation sequencing (NGS) methods have been broadly applied for analyzing patients with IRD. Here we report a novel approach to enrich the target...

Ful tanımlama

Kaydedildi:
Asıl Yazarlar: Xinjing Wang, Wadih M. Zein, Leera D’Souza, Chimere Roberson, Keith Wetherby, Hong He, Angela Villarta, Amy Turriff, Kory R. Johnson, Yang C. Fann
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMC 2017-08-01
Seri Bilgileri:BMC Ophthalmology
Konular:
Retinal
Microdroplet PCR
Next-generation-sequencing
Mutation screening
Online Erişim:http://link.springer.com/article/10.1186/s12886-017-0549-5
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller