Automated DNA mutation detection using universal conditions direct sequencing: application to ten muscular dystrophy genes

BACKGROUND: One of the most common and efficient methods for detecting mutations in genes is PCR amplification followed by direct sequencing. Until recently, the process of designing PCR assays has been to focus on individual assay parameters rather than concentrating on matching conditions for a se...

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Detalles Bibliográficos
Autores principales: Bennett, Richard R, Schneider, Hal E, Estrella, Elicia, Burgess, Stephanie, Cheng, Andrew S, Barrett, Caitlin, Lip, Va, Lai, Poh San, Shen, Yiping, Wu, Bai-Lin, Darras, Basil T, Beggs, Alan H, Kunkel, Louis M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2781300/
https://www.ncbi.nlm.nih.gov/pubmed/19835634
http://dx.doi.org/10.1186/1471-2156-10-66

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2781300/
https://www.ncbi.nlm.nih.gov/pubmed/19835634
http://dx.doi.org/10.1186/1471-2156-10-66

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