Robust sequence selection method used to develop the FluChip diagnostic microarray for influenza virus

被引:32
作者
Mehlmann, Martin
Dawson, Erica D.
Townsend, Michael B.
Smagala, James A.
Moore, Chad L.
Smith, Catherine B.
Cox, Nancy J.
Kuchta, Robert D.
Rowlen, Kathy L.
机构
[1] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80303 USA
[2] Ctr Dis Control & Prevent, Influenza Branch, Atlanta, GA 30333 USA
[3] InDevR LLC, Boulder, CO 80301 USA
关键词
D O I
10.1128/JCM.00135-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
DNA microarrays have proven to be powerful tools for gene expression analyses and are becoming increasingly attractive for diagnostic applications, e.g., for virus identification and subtyping. The selection of appropriate sequences for use on a microarray poses a challenge, particularly for highly mutable organisms such as influenza viruses, human immunodeficiency viruses, and hepatitis C viruses. The goal of this work was to develop an efficient method for mining large databases in order to identify regions of conservation in the influenza virus genome. From these regions of conservation, capture and label sequences capable of discriminating between different viral types and subtypes were selected. The salient features of the method were the use of phylogenetic trees for data reduction and the selection of a relatively small number of capture and label sequences capable of identifying a broad spectrum of influenza viruses. A detailed experimental evaluation of the selected sequences is described in a companion paper. The software is freely available under the General Public License at http://www.colorado.edu/chemistry/RGHP/software/.
引用
收藏
页码:2857 / 2862
页数:6
相关论文
共 29 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]   Dual-genome primer design for construction of DNA microarrays [J].
Andersson, A ;
Bernander, R ;
Nilsson, P .
BIOINFORMATICS, 2005, 21 (03) :325-332
[3]   Sequence versus structure for the direct detection of 16S rRNA on planar oligonucleotide microarrays [J].
Chandler, DP ;
Newton, GJ ;
Small, JA ;
Daly, DS .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (05) :2950-2958
[4]   A role for arrays in clinical virology: fact or fiction? [J].
Clewley, JP .
JOURNAL OF CLINICAL VIROLOGY, 2004, 29 (01) :2-12
[5]   The GPRIME package: computer programs for identifying the best regions of aligned genes to target in nucleic acid hybridisation-based diagnostic tests, and their use with plant viruses [J].
Gibbs, A ;
Armstrong, J ;
Mackenzie, AM ;
Weiller, GF .
JOURNAL OF VIROLOGICAL METHODS, 1998, 74 (01) :67-76
[6]   Primer design for large scale sequencing [J].
Haas, S ;
Vingron, M ;
Poustka, A ;
Wiemann, S .
NUCLEIC ACIDS RESEARCH, 1998, 26 (12) :3006-3012
[7]  
Hall T.A., 1999, NUCL ACIDS S SER, V41, P95, DOI DOI 10.1021/BK-1999-0734.CH008
[8]   MEGA3: Integrated software for molecular evolutionary genetics analysis and sequence alignment [J].
Kumar, S ;
Tamura, K ;
Nei, M .
BRIEFINGS IN BIOINFORMATICS, 2004, 5 (02) :150-163
[9]   Selection of optimal DNA oligos for gene expression arrays [J].
Li, FG ;
Stormo, GD .
BIOINFORMATICS, 2001, 17 (11) :1067-1076
[10]   Typing and subtyping influenza virus using DNA microarrays and multiplex reverse transcriptase PCR [J].
Li, JP ;
Chen, S ;
Evans, DH .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (02) :696-704