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Highlighting Differential Gene Expression between Two Condition Microarrays through Multidimensional Scaling Comparison of Lesihmania Infantum Genomic Data Similarity Matrices

机译:通过Leshmania Infantum基因组数据相似性矩阵的多维尺度比较突出两个条件微阵列之间的差异基因表达

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Classical methods for differential gene expression between two micro-array conditions often fail to detect interesting and important differences, because these appear too little compared to the expected variability. Data fusion has proved to highlight weak differences as it allows identifying genes associated to different biological conditions. However, data fusion often leads to a new representation of data, as for example in similarity matrices. Measuring distances between similarities for each gene is not a straightforward task, and methods for this would be useful in order to find potential genes for further research. Here, we present two different kernel methods based on multidimensional scaling and principal component analysis to measure distances between genes through an example on L. infantum microarrays comparing promastigote and amastigote stages. These methods are flexible and can be applied to any organism for which microarray and other genomic data is available.
机译:在两种微阵列条件之间差异基因表达的经典方法通常无法检测到有趣且重要的差异,因为与预期的变异性相比,这些差异显得很小。事实证明,数据融合突出了微弱的差异,因为它可以识别与不同生物学条件相关的基因。但是,数据融合通常会导致数据的新表示,例如在相似性矩阵中。测量每个基因的相似性之间的距离并不是一项简单的任务,为此目的,寻找潜在基因进行进一步研究的方法将是有用的。在这里,我们介绍了基于多维缩放和主成分分析的两种不同的核方法,以通过比较婴儿前鞭毛体和无鞭毛体阶段的婴儿乳杆菌微阵列上的示例来测量基因之间的距离。这些方法是灵活的,可以应用于可获得微阵列和其他基因组数据的任何生物。

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