Quantitative oligonucleotide microarray data analysis with an artificial standard probe strategy

被引:11
作者
Hwang, Byeong Hee [1 ]
Cha, Hyung Joon [1 ]
机构
[1] Pohang Univ Sci & Technol, Dept Chem Engn, Pohang 790784, South Korea
关键词
DNA chip; oligonucleotide microarray; quantitative data analysis; artificial standard probe;
D O I
10.1016/j.bios.2008.01.024
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Quantitative data analysis is an important element in several applications of DNA microarray, including mRNA expression profiling and estimation of infectious doses for pathogens. Here, we introduce an artificial standard probe strategy for quantitative pathogen detection using an oligonucleotide chip as a model system. The standard capture probe sequence was artificially designed to prevent non-specific hybridization with bacterial targets. Based on the fluorescence intensities of artificial standard spots, the raw fluorescence intensity data for specific spots could be corrected to generate linear correlations with target concentrations. Therefore, our novel artificial standard probe may be effectively applied for the correction of chip-to-chip variations and quantitative data analysis of a one-color labeled DNA microarray system. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1738 / 1744
页数:7
相关论文
共 17 条
[1]   Improved fluoroimmunoassays using the dye Alexa Fluor 647 with the RAPTOR, a fiber optic biosensor [J].
Anderson, GP ;
Nerurkar, NL .
JOURNAL OF IMMUNOLOGICAL METHODS, 2002, 271 (1-2) :17-24
[2]   Comparison of Alexa Fluor® and CyDye™ for practical DNA microarray use [J].
Ballard, Joanne L. ;
Peeva, Violet K. ;
deSilva, Christopher J. S. ;
Lynch, Jessica L. ;
Swanson, Nigel R. .
MOLECULAR BIOTECHNOLOGY, 2007, 36 (03) :175-183
[3]   Comparative genomics of BCG vaccines by whole-genome DNA microarray [J].
Behr, MA ;
Wilson, MA ;
Gill, WP ;
Salamon, H ;
Schoolnik, GK ;
Rane, S ;
Small, PM .
SCIENCE, 1999, 284 (5419) :1520-1523
[4]   Amplification of whole tumor genomes and geneby-gene mapping of genomic aberrations from limited sources of fresh-frozen and paraffin-embedded DNA [J].
Bredel, M ;
Bredel, C ;
Juric, D ;
Kim, Y ;
Vogel, H ;
Harsh, GR ;
Recht, LD ;
Pollack, JR ;
Sikic, BI .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2005, 7 (02) :171-182
[5]   Quantitative detection of microbial genes by using DNA microarrays [J].
Cho, JC ;
Tiedje, JM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2002, 68 (03) :1425-1430
[6]   Multiple detection of food-borne pathogenic bacteria using a novel 16S rDNA-based oligonucleotide signature chip [J].
Eom, Ho Seop ;
Hwang, Byeong Hee ;
Kim, Duk-Hee ;
Lee, In-Beum ;
Kim, Young Hee ;
Cha, Hyung Joon .
BIOSENSORS & BIOELECTRONICS, 2007, 22 (06) :845-853
[7]   Oligonucleotide microchips as genosensors for determinative and environmental studies in microbiology [J].
Guschin, DY ;
Mobarry, BK ;
Proudnikov, D ;
Stahl, DA ;
Rittmann, BE ;
Mirzabekov, AD .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (06) :2397-2402
[8]   DNA microarray technology: Devices, systems, and applications [J].
Heller, MJ .
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, 2002, 4 :129-153
[9]   Discovery and analysis of inflammatory disease-related genes using cDNA microarrays [J].
Heller, RA ;
Schena, M ;
Chai, A ;
Shalon, D ;
Bedilion, T ;
Gilmore, J ;
Woolley, DE ;
Davis, RW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2150-2155
[10]   Three color cDNA microarrays: quantitative assessment through the use of fluorescein-labeled probes [J].
Hessner, MJ ;
Wang, XJ ;
Hulse, K ;
Meyer, L ;
Wu, Y ;
Nye, S ;
Guo, SW ;
Ghosh, S .
NUCLEIC ACIDS RESEARCH, 2003, 31 (04) :e14