Single-well genotyping of diallelic sequence variations by a two-color ELISA-based oligonucleotide ligation assay.
Single nucleotide substitutions and unique insertions/deletions are the most common form of DNA sequence variation and disease-causing mutation in the human genome. Because of the biological and medical importance of these variations, a wide array of methods have been developed for their typing. We...
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| Vydáno v: | Nucleic Acids Res |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
1996
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC146169/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8871551/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/24.19.3728 |
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