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Statistical evaluation of differential expression on cDNA nylon arrays with replicated experiments

机译:使用重复实验对cDNA尼龙阵列上差异表达的统计学评估

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In this paper we focus on the detection of differentially expressed genes according to changes in hybridization signals using statistical tests. These tests were applied to 14 208 zebrafish cDNA clones that were immobilized on a nylon support and hybridized with radioactively labeled target mRNA from wild-type and lithium-treated zebrafish embryos. The methods were evaluated with respect to 16 control clones that correspond to eight different genes which are known to be involved in dorso-ventral axis specification. Moreover, 4608 Arabidopsis thaliana clones on the same array were used to judge statistical significance of expression changes and to control the false positive rates of the test decisions. Utilizing this special array design we show that differential expression of a high proportion of cDNA clones (15/16) and the respective genes (7/8) were identified, with a false positive error of <5% using the constant control data. Furthermore, we investigated the influence of the number of repetitions of experiments on the accuracy of the procedures with experimental and simulated data. Our results suggest that the detection of differential expression with repeated hybridization experiments is an accurate and sensitive way of identifying even small expression changes (1:1.5) of a large number of genes in parallel.
机译:在本文中,我们着重于利用统计检验根据杂交信号的变化检测差异表达基因。这些测试应用于14 208个斑马鱼cDNA克隆,这些克隆固定在尼龙支持物上,并与来自野生型和锂处理过的斑马鱼胚胎的放射性标记的目标mRNA杂交。针对16种对照克隆评估了该方法,这些克隆对应于八个不同的基因,这些基因已知参与背腹轴的规范。此外,在同一阵列上的4608拟南芥克隆用于判断表达变化的统计学意义并控制测试决定的假阳性率。利用这种特殊的阵列设计,我们显示,使用恒定的对照数据,可以鉴定出高比例的cDNA克隆(15/16)和各个基因(7/8)的差异表达,假阳性误差<5%。此外,我们用实验和模拟数据研究了实验重复次数对程序准确性的影响。我们的结果表明,通过重复杂交实验检测差异表达是一种准确,灵敏的方法,可以并行识别甚至大量基因的微小表达变化(1:1.5)。

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