English Sangeeta B, Shih Shou-Ching, Ramoni Marco F, Smith Lois E, Butte Atul J
Stanford Center for Biomedical Informatics Research (BMIR), Stanford University School of Medicine, 251 Campus Drive, Stanford, CA 94305, USA.
J Biomed Inform. 2009 Apr;42(2):287-95. doi: 10.1016/j.jbi.2008.08.009. Epub 2008 Aug 26.
Though genome-wide technologies, such as microarrays, are widely used, data from these methods are considered noisy; there is still varied success in downstream biological validation. We report a method that increases the likelihood of successfully validating microarray findings using real time RT-PCR, including genes at low expression levels and with small differences. We use a Bayesian network to identify the most relevant sources of noise based on the successes and failures in validation for an initial set of selected genes, and then improve our subsequent selection of genes for validation based on eliminating these sources of noise. The network displays the significant sources of noise in an experiment, and scores the likelihood of validation for every gene. We show how the method can significantly increase validation success rates. In conclusion, in this study, we have successfully added a new automated step to determine the contributory sources of noise that determine successful or unsuccessful downstream biological validation.
尽管全基因组技术,如微阵列,被广泛应用,但这些方法得到的数据被认为存在噪声;在下游生物学验证中仍有不同程度的成功。我们报告了一种方法,该方法使用实时逆转录聚合酶链反应(real time RT-PCR)提高成功验证微阵列结果的可能性,包括低表达水平和差异较小的基因。我们使用贝叶斯网络根据一组初始选定基因验证的成功与失败来识别最相关的噪声源,然后基于消除这些噪声源来改进我们后续用于验证的基因选择。该网络展示了实验中显著的噪声源,并对每个基因的验证可能性进行评分。我们展示了该方法如何能显著提高验证成功率。总之,在本研究中,我们成功添加了一个新的自动化步骤来确定决定下游生物学验证成功或失败的噪声的促成来源。