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Systematic Evaluation of Gene Expression Data Analysis Methods Using Benchmark Data

机译:基因表达数据分析方法的系统评估使用基准数据

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Due to limited amount of experimental validation datasets, data analysis methods for identifying differential expression based on high-throughput expression profiling technologies such as microarray and RNA-seq cannot be statistically validated properly, and thus guidelines for selecting an appropriate method are lacking. We applied mRNA spike-in approaches to develop a comprehensive set of experimental benchmark data and used it to evaluate various methods for identification of differential expression. Our results show that using the median log ratio to identify differential expression is superior to more complex and popular methods such as modified t-statistics. The median log ratio method is robust that a reasonably high accuracy of identification of differentially expressed genes can be achieved even for data with a small number of replicates and strong experimental variation between replicates. Machine learning for classification of differential expression based on the benchmark dataset indicates the existence of even more accurate methods for identification of differential expression. With this dataset, it can be also demonstrated that the methods prediction of false discovery rate based on a small number of replicates could be very inaccurate.
机译:由于实验验证数据集数量有限,可以正确地验证基于微阵列和RNA-SEQ等高通量表达分析技术的鉴定差异表达的数据分析方法不能统计验证,因此缺乏用于选择合适方法的指导。我们应用MRNA Spike-in Windes开发一套全面的实验基准数据,并用它来评估各种方法以识别差异表达。我们的结果表明,使用中位数对数比识别差异表达优于更复杂和流行的方法,如修改的T统计。中值对数比方法是强大的,即使对于具有少量重复的数据以及复制之间的强实验变化,可以实现相当高的差异表达基因的鉴定精度。基于基于基准数据集的差异表达式分类的机器学习表示存在更准确的方法来识别差异表达。使用此数据集,还可以说明基于少量复制的错误发现率的方法可能非常不准确。

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