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Oligonucleotide gap-fill ligation for mutation detection and sequencing in situ
In clinical diagnostics a great need exists for targeted in situ multiplex nucleic acid analysis as the mutational status can offer guidance for effective treatment. One well-established method uses padlock probes for mutation detection and multiplex expression analysis directly in cells and tissues...
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| Publicado no: | Nucleic Acids Res |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4678841/ https://ncbi.nlm.nih.gov/pubmed/26240388 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkv772 |
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