Illumina sequencing of 15 deafness genes using fragmented amplicons

BACKGROUND: Resequencing of deafness related genes using GS FLX massive parallel sequencing of PCR amplicons spanning selected genes has previously been reported as a successful strategy to discover causal variants. The amplicon lengths were designed to be smaller than the sequencing read length of...

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Detaylı Bibliyografya
Yayımlandı:BMC Res Notes
Asıl Yazarlar: Van Nieuwerburgh, Filip, De Keulenaer, Sarah, De Schrijver, Joachim, Vandesompele, Jo, Van Criekinge, Wim, Coucke, Paul J, Deforce, Dieter
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2014
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4266979/
https://ncbi.nlm.nih.gov/pubmed/25106482
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1756-0500-7-509
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