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Evaluating single-subject study methods for personal transcriptomic interpretations to advance precision medicine

机译:评估个人转录组解释的单项研究方法以提高精密医学水平

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Gene expression profiling has benefited medicine by providing clinically relevant insights at the molecular candidate and systems levels. However, to adopt a more ‘precision’ approach that integrates individual variability including ‘omics data into risk assessments, diagnoses, and therapeutic decision making, whole transcriptome expression needs to be interpreted meaningfully for single subjects. We propose an “all-against-one” framework that uses biological replicates in isogenic conditions for testing differentially expressed genes (DEGs) in a single subject (ss) in the absence of an appropriate external reference standard or replicates. To evaluate our proposed “all-against-one” framework, we construct reference standards (RSs) with five conventional replicate-anchored analyses (NOISeq, DEGseq, edgeR, DESeq, DESeq2) and the remainder were treated separately as single-subject sample pairs for ss analyses (without replicates). Eight ss methods (NOISeq, DEGseq, edgeR, mixture model, DESeq, DESeq2, iDEG, and ensemble) for identifying genes with differential expression were compared in Yeast (parental line versus snf2 deletion mutant; n?=?42/condition) and a MCF7 breast-cancer cell line (baseline versus stimulated with estradiol; n?=?7/condition). Receiver-operator characteristic (ROC) and precision-recall plots were determined for eight ss methods against each of the five RSs in both datasets. Consistent with prior analyses of these data, ~?50% and ~?15% DEGs were obtained in Yeast and MCF7 datasets respectively, regardless of the RSs method. NOISeq, edgeR, and DESeq were the most concordant for creating a RS. Single-subject versions of NOISeq, DEGseq, and an ensemble learner achieved the best median ROC-area-under-the-curve to compare two transcriptomes without replicates regardless of the RS method and dataset (?90% in Yeast, ?0.75 in MCF7). Further, distinct specific single-subject methods perform better according to different proportions of DEGs. The “all-against-one” framework provides a honest evaluation framework for single-subject DEG studies since these methods are evaluated, by design, against reference standards produced by unrelated DEG methods. The ss-ensemble method was the only one to reliably produce higher accuracies in all conditions tested in this conservative evaluation framework. However, single-subject methods for identifying DEGs from paired samples need improvement, as no method performed with precision?90% and obtained moderate levels of recall.
机译:通过在候选分子和系统水平上提供与临床相关的见解,基因表达谱已使医学受益。但是,要采用一种更加“精确”的方法来将包括“组学数据”在内的个体变异性整合到风险评估,诊断和治疗决策中,则需要对单个受试者有意义地解释整个转录组的表达。我们提出了一个“万无一失”的框架,该框架在等基因条件下使用生物学复制品,在没有合适的外部参考标准或复制品的情况下测试单个受试者(ss)中的差异表达基因(DEG)。为了评估我们提出的“全反对一”框架,我们用五个常规的重复锚定分析(NOISeq,DEGseq,edgeR,DESeq,DESeq2)构建了参考标准(RS),其余分别作为单对象样本对处理。用于ss分析(无重复)。在酵母中比较了八种ss方法(NOISeq,DEGseq,edgeR,混合模型,DESeq,DESeq2,iDEG和系综),用于鉴定具有差异表达的基因(亲本系与snf2缺失突变体; n == 42 /条件)和MCF7乳腺癌细胞系(基线与雌二醇刺激的基线; n == 7 /条件)。针对两个数据集中的五个RS中的每一个,针对八个ss方法确定了接收器-操作员特征(ROC)和精确调用图。与这些数据的先前分析一致,无论采用RSs方法如何,分别在Yeast和MCF7数据集中获得~~ 50%和~~ 15%的DEG。 NOISeq,edgeR和DESeq是创建RS时最一致的。单主题版本的NOISeq,DEGseq和整体学习者获得了最佳的ROC中值曲线下区域,以比较两个无重复的转录组,而与RS方法和数据集无关(Yeast中> 90%,> 0.75)在MCF7中)。此外,根据DEG的不同比例,不同的特定单对象方法效果更好。 “完全反对”框架为单科目的DEG研究提供了一个诚实的评估框架,因为这些方法是根据设计依据非相关DEG方法产生的参考标准进行评估的。在这种保守的评估框架中测试的所有条件下,ss集成方法都是唯一能够可靠地产生更高精度的方法。但是,用于从配对样本中识别DEG的单对象方法需要改进,因为没有一种方法能以> 90%的精确度进行检索并且获得中等水平的查全率。

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