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A robust protocol to increase NimbleGen SeqCap EZ multiplexing capacity to 96 samples.
van der Werf, Ilse M; Kooy, R Frank; Vandeweyer, Geert.
Afiliação
  • van der Werf IM; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
  • Kooy RF; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
  • Vandeweyer G; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
PLoS One ; 10(4): e0123872, 2015.
Article em En | MEDLINE | ID: mdl-25875648
ABSTRACT
Contemporary genetic studies frequently involve sequencing of a targeted gene panel, for instance consisting of a set of genes associated with a specific disease. The NimbleGen SeqCap EZ Choice kit is commonly used for the targeted enrichment of sequencing libraries comprising a target size up to 7 Mb. A major drawback of this commercially available method is the exclusive use of single-indexing, meaning that at most 24 samples can be multiplexed in a single reaction. In case of relatively small target sizes, this will lead to excessive amounts of data per sample. We present an extended version of the NimbleGen SeqCap EZ protocol which allows to robustly multiplex up to 96 samples. We achieved this by incorporating Illumina dual-indexing based custom adapters into the original protocol. To further extend the optimization of cost-efficient sequencing of custom target panels, we studied the effect of higher pre-enrichment pooling factors and show that pre-enrichment pooling of up to 12 samples does not affect the quality of the data. To facilitate evaluation of capture efficiency in custom design panels, we also provide a detailed reporting tool.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise de Sequência de DNA / Sequenciamento de Nucleotídeos em Larga Escala Limite: Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise de Sequência de DNA / Sequenciamento de Nucleotídeos em Larga Escala Limite: Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Bélgica