Bauer Andrea, Beckmann Boris, Busold Christian, Brandt Ole, Kusnezow Wlad, Pullat Janne, Aign Verena, Fellenberg Kurt, Fleischer Robert, Jacob Anette, Frohme Marcus, Hoheisel Jörg D
Division of Functional Genome Analysis, Deutsches Krebsforschungszentrum (DKFZ), Im Neuenheimer Feld 580, Heidelberg D-69120, Germany.
Comp Funct Genomics. 2003;4(5):520-4. doi: 10.1002/cfg.320.
While the deciphering of basic sequence information on a genomic scale is yielding complete genomic sequences in ever-shorter intervals, experimental procedures for elucidating the cellular effects and consequences of the DNA-encoded information become critical for further analyses. In recent years, DNA microarray technology has emerged as a prime candidate for the performance of many such functional assays. Technically, array technology has come a long way since its conception some 15 years ago, initially designed as a means for large-scale mapping and sequencing.The basic arrangement, however, could be adapted readily to serve eventually as an analytical tool in a large variety of applications. On their own or in combination with other methods, microarrays open up many new avenues of functional analysis.
虽然在基因组规模上对基本序列信息的解读正以越来越短的间隔产生完整的基因组序列,但阐明DNA编码信息的细胞效应和后果的实验程序对于进一步分析变得至关重要。近年来,DNA微阵列技术已成为进行许多此类功能测定的主要候选技术。从技术上讲,阵列技术自约15年前诞生以来已经取得了长足的发展,最初设计为大规模映射和测序的手段。然而,其基本布局可以很容易地进行调整,最终用作各种应用中的分析工具。微阵列单独使用或与其他方法结合使用,开辟了许多新的功能分析途径。