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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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| Publicado no: | BMC Res Notes |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2014
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| Assuntos: | |
| Acesso em linha: | 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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