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1.
Methods Enzymol ; 410: 3-28, 2006.
Article in English | MEDLINE | ID: mdl-16938544

ABSTRACT

The intent of this chapter is to provide the reader with a review of GeneChip technology and the complete system it represents, including its versatility, components, and the exciting applications that are enabled by this platform. The following aspects of the technology are reviewed: array design and manufacturing, target preparation, instrumentation, data analysis, and both current and future applications. There are key differentiators between Affymetrix' GeneChip technology and other microarray-based methods. The most distinguishing feature of GeneChip microarrays is that their manufacture is directed by photochemical synthesis. Because of this manufacturing technology, more than a million different probes can be synthesized on an array roughly the size of a thumbnail. These numbers allow the inclusion of multiple probes to interrogate the same target sequence, providing statistical rigor to data interpretation. Over the years the GeneChip platform has proven to be a reliable and robust system, enabling many new discoveries and breakthroughs to be made by the scientific community.


Subject(s)
Oligonucleotide Array Sequence Analysis/instrumentation , Oligonucleotide Array Sequence Analysis/methods , Animals , Humans
2.
Methods Mol Biol ; 258: 71-94, 2004.
Article in English | MEDLINE | ID: mdl-14970458

ABSTRACT

An increasing number of biological and medical research questions depend on obtaining global views of gene expression. In this chapter, we will describe how oligonucleotide microarrays have been used to accomplish this goal. In particular, we will focus on the use of GeneChip arrays, which provide high levels of reproducibility, sensitivity, and specificity. Target preparation, hybridization, washing, signal detection, and data analysis will be described in detail. Additionally, we will discuss options for facilitating data sharing, including the creation of databases, and the use of internet tools that help users place their results in the context of data from public and proprietary databases. There is so much interest and innovation in the field of genomics that protocols are constantly evolving. This chapter should be used as a genomic profiling guide only. We urge readers to consult www.affymetrix.com for the most current products and protocols.


Subject(s)
Eukaryotic Cells/physiology , Gene Expression Profiling/methods , Gene Expression/physiology , Oligonucleotide Array Sequence Analysis/methods , Animals , Humans , RNA, Messenger/analysis
3.
Pharmacogenomics ; 3(5): 589-601, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12223046

ABSTRACT

With their ability to provide global views of genome sequence and gene activity, microarrays have emerged as key analytical tools in the field of pharmacogenomics. Vast amounts of data must be collected and analyzed to meet pharmacogenomics' ambitious goals, ranging from identifying markers that predict individuals' responses to therapy to discovering new drug targets. Microarrays will be instrumental to these efforts because they provide bountiful sources of gene expression and genotypic data. Attesting to their productivity, microarrays have been the central technology used in thousands of peer-reviewed publications and have also become important contributors to many databases including PharmGKB, the Cancer Microarray Database and the database of single nucleotide polymorphisms (dbSNP). Microarrays are also making more focused contributions, however, in helping pursue hypothesis-driven inquiries that extend or complement broad genomic surveys. In addition, their potential as clinical tools is being increasingly recognized. This review identifies some of the varied and changing needs of pharmacogenomics research and discusses the ways in which microarrays are tending to these demands. The technique's strongpoints and limitations are examined, as well as its future potential.


Subject(s)
Oligonucleotide Array Sequence Analysis/trends , Pharmacogenetics/trends , Gene Expression/genetics , Genotype , Humans , Oligonucleotide Array Sequence Analysis/methods , Pharmacogenetics/methods , Phenotype
4.
Genet Epidemiol ; 23(1): 4-20, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12112245

ABSTRACT

The advent of molecular technologies that allow the collection and analysis of large amounts of genetic data is rapidly transforming the field of genetic epidemiology. Whether monitoring infectious outbreaks or identifying genotypic variations that underlie disease susceptibility, genetic epidemiology relies heavily on the analysis of multiple, independently derived results. By allowing the simultaneous monitoring of thousands of genetic or expression data points, microarrays are emerging as particularly powerful tools. Several recent reviews have described array manufacturing and the types of scientific questions that can exploit this technology, but few have addressed how the intended use of an array can dictate its design. This review will focus on this latter issue, with particular emphasis on the genetic epidemiology of infectious disease. The design of arrays for genotyping, expression profiling, and fingerprinting are presented, and examples of recent epidemiological studies are used to illustrate the applications' strong points and limitations. In addition to discussing arrays' ability to provide global views of gene identity or function, the review will describe design options for creating arrays that detect multiple genetic variations. It will also examine the reliability of array-generated fingerprints, assay accessibility, and possibilities for sharing and comparing data across studies. Although many challenges lie ahead, microarrays' multiple abilities appear uniquely poised to accelerate the advance of genetic epidemiology's multiple fronts.


Subject(s)
DNA/genetics , Epidemiologic Methods , Infections/genetics , Oligonucleotide Array Sequence Analysis , Base Sequence , DNA/chemistry , DNA Probes , Genetic Variation , Humans , Infections/epidemiology , Reproducibility of Results , Research Design
5.
Psychiatr Genet ; 12(2): 97-107, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12131762

ABSTRACT

Small variations in human DNA sequences influence our predisposition to disease and our response to medications. Many psychiatric diseases appear to be polygenic. Because our molecular understanding of the genetic etiology of neuropsychiatric disorders is very limited, the discovery and characterization of these variations is crucial in identifying disease genes. Furthermore, this knowledge may enable the customized selection of drug treatments based on an individual's genotype so as to maximize efficacy yet avoid adverse side effects. Examples of findings using conventional methods for determining genotypes, as well as new and future technologies for the characterization of single nucleotide polymorphisms, will be discussed, with a focus on psychiatric diseases and medications.


Subject(s)
Mental Disorders/genetics , Nervous System Diseases/genetics , Oligonucleotide Array Sequence Analysis/methods , Polymorphism, Single Nucleotide , Base Sequence , Bipolar Disorder/genetics , DNA/genetics , Genetic Variation , Humans , Parkinson Disease/genetics , Polymorphism, Genetic
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