Literature DB >> 11933189

Analysis of SNPs and other genomic variations using gel-based chips.

Alexander Kolchinsky1, Andrei Mirzabekov.   

Abstract

Application of microarrays for the analysis of point mutations and SNPs in genomic DNAs is currently under intensive development. Various technologies are being investigated, employing enzymatic, chemical, and physical tools [for review, see Tillib and Mirzabekov, 2001]. Our current approach is based on the use of IMAGE chips (immobilized microarrays of gel elements) consisting of an array of gel pads attached to a hydrophobic glass surface. The gel pads range in size from picoliters to nanoliters and are used for immobilization of oligonucleotide probes, as well as miniature test tubes for chemical or enzymatic reactions with tethered compounds. Nucleic acids are hybridized, fractionated, modified, and subjected to enzymatic reactions inside the pads. All steps of sequence analysis (PCR-amplification, activation or release of primers and products, DNA extension, hybridization, and reading of the results) can be performed within the same pad. A flexible and inexpensive technology platform enables one to monitor processes in the arrays in both real time and steady-state. Identification of SNPs, microsequencing, and other specific tasks are easily performed. In particular, stacking interactions with short oligonucleotides enhance the capability of high-throughput screening. The IMAGE chips can be analyzed using a variety of equipment, from a dedicated multi-color fluorescent microscope or MALDI-spectrometer to an inexpensive portable analyzer suitable for field conditions. Customized gel-based chips were successfully used for screening of SNPs in a broad range of biologically meaningful genes. Copyright 2002 Wiley-Liss, Inc.

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Mesh:

Year:  2002        PMID: 11933189     DOI: 10.1002/humu.10077

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  5 in total

1.  Generation of hydroxyapatite patterns by electrophoretic deposition.

Authors:  Seiji Yamaguchi; Takeshi Yabutsuka; Mitsuhiro Hibino; Takeshi Yao
Journal:  J Mater Sci Mater Med       Date:  2007-10-04       Impact factor: 3.896

2.  Comparisons of substitution, insertion and deletion probes for resequencing and mutational analysis using oligonucleotide microarrays.

Authors:  Mazen W Karaman; Susan Groshen; Chi-Chiang Lee; Brian L Pike; Joseph G Hacia
Journal:  Nucleic Acids Res       Date:  2005-02-18       Impact factor: 16.971

Review 3.  Efficient SNP Discovery by Combining Microarray and Lab-on-a-Chip Data for Animal Breeding and Selection.

Authors:  Chao-Wei Huang; Yu-Tsung Lin; Shih-Torng Ding; Ling-Ling Lo; Pei-Hwa Wang; En-Chung Lin; Fang-Wei Liu; Yen-Wen Lu
Journal:  Microarrays (Basel)       Date:  2015-11-16

4.  Influence of the length of target DNA overhang proximal to the array surface on discrimination of single-base mismatches on a 25-mer oligonucleotide array.

Authors:  Jenny Tomlinson; Catherine Harrison; Neil Boonham; Sarah A Goodchild; Simon A Weller
Journal:  BMC Res Notes       Date:  2014-04-17

5.  Oligonucleotide microchip for subtyping of influenza A virus.

Authors:  Eugeny E Fesenko; Dmitry E Kireyev; Dmitry A Gryadunov; Vladimir M Mikhailovich; Tatyana V Grebennikova; Dmitry K L'vov; Alexander S Zasedatelev
Journal:  Influenza Other Respir Viruses       Date:  2007-05       Impact factor: 4.380

  5 in total

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