Channel Glass-based Detection of Human Short Insertion/ Deletion Polymorphisms by Tandem Hybridization

dc.contributor.authorBetanzos Cabrera, Gabrielen_US
dc.date.accessioned2013-11-05T22:04:49Z
dc.date.available2013-11-05T22:04:49Z
dc.date.issued2008en_US
dc.description.abstractThe development and critical evaluation of newtechnologies for identifying genetic polymorphisms willrapidly accelerate the discovery and diagnosis of diseaserelatedgenes. We report a novel way for distinguishing anew class of human DNA polymorphisms, short insertion/deletion polymorphisms (indels). A sensor with cylindricalpores named channel glass in combination with tandemhybridization, which uses a 50-fluorescent labeled stackingprobe and microarray-based short allele-specificoligonucleotide (capture probe) was investigated. Thismethodology allows indels to be detected individuallyand rapidly with small quantities of target DNA. Thisestablishes a reliable quantitative test. Approaches forsimultaneously hybridizing different targets to arrayedprobes, designed to detect various indels in parallel, wereexamined. Five markers were consistently detected in asingle hybridization. Possible factors impeding thehybridization reaction process are discussed.es
dc.identifier.citationGabriel Betanzos-Cabrera, Brent W. Harker,Mitchel J. Doktycz, James L. Weber y Kenneth L. Beattie. (2008). Channel Glass-based Detection of Human Short Insertion/Deletion Polymorphisms by Tandem Hybridization. Mol Biotechnol 38:145153 DOI 10.1007/s12033-007-9004-9es
dc.identifier.urihttps://repository.uaeh.edu.mx/bitstream/handle/123456789/11979
dc.languageesen_US
dc.subjectNutrición Moleculares
dc.titleChannel Glass-based Detection of Human Short Insertion/ Deletion Polymorphisms by Tandem Hybridizationes
dc.typeArticleen_US

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