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Exploiting dependencies of pairwise comparison outcomes to predict patterns of gene response

机译:利用成对比较结果的依赖性来预测基因应答模式

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Background The analysis of gene expression has played an important role in medical and bioinformatics research. Although it is known that a large number of samples is needed to determine the patterns of gene expression accurately, practical designs of gene expression studies occasionally have insufficient numbers of samples, making it difficult to ascertain true response patterns of variantly expressed genes. Results We describe an approach to cope with the challenge of predicting true orders of gene response to treatments. We show that true patterns of gene response must be orderable sets. In experiments with few samples, we modify the conventional pairwise comparison tests and increase the significance level α intelligently to deduce orderable patterns, which are most likely true orders of gene response. Additionally, motivated by the fact that a gene can be involved in multiple biological functions, our method further resamples experimental replicates and predicts multiple response patterns for each gene. Using a gene expression data set of Sprague-Dawley rats treated with chemopreventive chemical compounds and DAVID to annotate and validate gene sets, we showed that compared to the conventional method of fixing α , this method increased enrichment significantly. A comparison with hierarchical clustering showed that gene clusters labelled by response patterns produced by our method were much more enriched. One of the clusters contained 3 transcription factors, which hierarchical clustering failed to place into one cluster, that have been found to participate in multiple biological networks. One of the transcription factors is known to play an important role in pathways affected by the studied chemical compounds. Conclusions This method can be useful in designing cost-effective experiments with small sample sizes. Patterns of highly-variantly expressed genes can be predicted by varying α intelligently. Furthermore, clusters are labeled meaningfully with patterns that describe precisely how genes in such clusters respond to treatments.
机译:背景技术基因表达分析在医学和生物信息学研究中发挥了重要作用。尽管已知需要大量样本来准确确定基因表达的模式,但是基因表达研究的实际设计偶尔会遇到样本数量不足的情况,这使得难以确定变异表达基因的真实应答模式。结果我们描述了一种应对预测基因对治疗反应的真实顺序的挑战的方法。我们表明基因反应的真实模式必须是可排序的集。在样本较少的实验中,我们修改了常规的成对比较测试,并智能地提高了显着性水平α以推论有序模式,这很可能是基因反应的真正顺序。此外,受基因可以参与多种生物学功能的事实启发,我们的方法进一步对实验重复样本进行了重新采样,并预测了每个基因的多种反应模式。使用化学预防化合物和DAVID处理的Sprague-Dawley大鼠的基因表达数据集来注释和验证基因集,我们证明,与固定a的常规方法相比,该方法显着增加了富集。与分层聚类的比较表明,用我们的方法产生的应答模式标记的基因簇更加丰富。其中一个簇包含3个转录因子,这些分层因子未能放置到一个簇中,已发现它们参与了多个生物网络。已知转录因子之一在受研究化合物影响的途径中起重要作用。结论该方法可用于设计小样本量的具有成本效益的实验。可以通过智能地改变α来预测高度变异表达基因的模式。此外,簇被有意义地标记有模式,该模式精确描述了这些簇中的基因如何响应治疗。

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