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Analysis of matched mRNA measurements from two different microarray technologies

机译:分析来自两种不同微阵列技术的匹配mRNA测量

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Motivation: The existence of several technologies for measuring gene expression makes the question of cross-technology agreement of measurements an important issue. Cross-platform utilization of data from different technologies has the potential to reduce the need to duplicate experiments but requires corresponding measurements to be comparable. Methods: A comparison of mRNA measurements of 2895 sequence-matched genes in 56 cell lines from the standard panel of 60 cancer cell lines from the National Cancer Institute (NCI 60) was carried out by calculating correlation between matched measurements and calculating concordance between cluster from two high-throughput DNA microarray technologies, Stanford type cDNA microarrays and Affymetrix oligonucleotide microarrays. Results: In general, corresponding measurements from the two platforms showed poor correlation. Clusters of genes and cell lines were discordant between the two technologies, suggesting that relative intra-technology relationships were not preserved. GC-content, sequence length, average signal intensity, and an estimator of cross-hybridization were found to be associated with the degree of correlation. This suggests gene-specific, or more correctly probe-specific, factors influencing measurements differently in the two platforms, implying a poor prognosis for a broad utilization of gene expression measurements across platforms.
机译:动机:几种用于测量基因表达的技术的存在使跨技术的测量一致性问题成为一个重要的问题。来自不同技术的数据的跨平台利用有可能减少重复实验的需要,但需要相应的测量结果才具有可比性。方法:通过计算匹配的测量值之间的相关性,并计算来自美国国家癌症研究所的60个癌细胞系的标准组(NCI 60)中的56个细胞系的标准组中的2895个序列匹配基因的mRNA测量值,进行比较。两种高通量DNA微阵列技术,Stanford型cDNA微阵列和Affymetrix寡核苷酸微阵列。结果:通常,来自两个平台的相应测量显示出很差的相关性。两种技术之间基因和细胞系的簇不一致,表明没有保留相对的技术内关系。发现GC含量,序列长度,平均信号强度和交叉杂交的估计量与相关程度有关。这表明在两个平台中影响测量的基因特异性或更正确探针特异性的因素,暗示跨平台广泛使用基因表达测量的预后不良。

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