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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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Published in:Nucleic Acids Res
Main Authors: Tobe, V O, Taylor, S L, Nickerson, D A
Format: Artigo
Language:Inglês
Published: Oxford University Press 1996
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Research Article
Online Access: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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