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Homogeneous point mutation detection by quantum dot-mediated two-color fluorescence coincidence analysis
This report describes a new genotyping method capable of detecting low-abundant point mutations in a homogeneous, separation-free format. The method is based on integration of oligonucleotide ligation with a semiconductor quantum dot (QD)-mediated two-color fluorescence coincidence detection scheme....
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2006
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1390686/ https://ncbi.nlm.nih.gov/pubmed/16517937 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkl021 |
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