Abstract
The development and critical evaluation of new technologies for identifying genetic polymorphisms will rapidly accelerate the discovery and diagnosis of disease-related genes. We report a novel way for distinguishing a new class of human DNA polymorphisms, short insertion/deletion polymorphisms (indels). A sensor with cylindrical pores named channel glass in combination with tandem hybridization, which uses a 5′-fluorescent labeled stacking probe and microarray-based short allele-specific oligonucleotide (capture probe) was investigated. This methodology allows indels to be detected individually and rapidly with small quantities of target DNA. This establishes a reliable quantitative test. Approaches for simultaneously hybridizing different targets to arrayed probes, designed to detect various indels in parallel, were examined. Five markers were consistently detected in a single hybridization. Possible factors impeding the hybridization reaction process are discussed.
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Financial support for this work was provided by PROMEP/103.5/03/1130, Fondo Sectorial Área de Ciencia Básica SEP-CONACYT 2004-C01-46537, PA144B-2007 and by NIH grant R01 HL62681-01.
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Betanzos-Cabrera, G., Harker, B.W., Doktycz, M.J. et al. Channel Glass-based Detection of Human Short Insertion/Deletion Polymorphisms by Tandem Hybridization. Mol Biotechnol 38, 145–153 (2008). https://doi.org/10.1007/s12033-007-9004-9
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DOI: https://doi.org/10.1007/s12033-007-9004-9