基因表达数据的缺失值估算方法。

Pub Date : 2017-04-25 DOI:10.1515/sagmb-2015-0098
Shahla Faisal, Gerhard Tutz
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引用次数: 17

摘要

像基因表达和rna序列这样的高维数据经常包含缺失值。基于这些不完整数据的后续分析和结果可能会受到这些缺失值的严重影响。基因表达数据缺失值的估算方法已经发展起来,但由于数据的高维数(基因数量),任务比较困难。本文提出了一种加权最近邻法的插值方法。不是使用包含所有基因的距离定义的最近邻,而是计算易于对输入值的准确性做出贡献的基因的距离。该方法旨在避免在高维环境中应用作为最近邻的局部方法通常会出现的维数诅咒。将所提出的加权最近邻算法与现有的缺失值imputation技术如mean imputation、KNNimpute和最近提出的随机森林imputation进行了比较。我们使用来自人类癌症研究的rna序列和微阵列数据来比较这些方法的性能。仿真和实际研究结果表明,加权距离方法可以成功地处理预测数大于样本数的高维数据结构的缺失值。该方法通常优于考虑过的竞争对手。
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Missing value imputation for gene expression data by tailored nearest neighbors.

High dimensional data like gene expression and RNA-sequences often contain missing values. The subsequent analysis and results based on these incomplete data can suffer strongly from the presence of these missing values. Several approaches to imputation of missing values in gene expression data have been developed but the task is difficult due to the high dimensionality (number of genes) of the data. Here an imputation procedure is proposed that uses weighted nearest neighbors. Instead of using nearest neighbors defined by a distance that includes all genes the distance is computed for genes that are apt to contribute to the accuracy of imputed values. The method aims at avoiding the curse of dimensionality, which typically occurs if local methods as nearest neighbors are applied in high dimensional settings. The proposed weighted nearest neighbors algorithm is compared to existing missing value imputation techniques like mean imputation, KNNimpute and the recently proposed imputation by random forests. We use RNA-sequence and microarray data from studies on human cancer to compare the performance of the methods. The results from simulations as well as real studies show that the weighted distance procedure can successfully handle missing values for high dimensional data structures where the number of predictors is larger than the number of samples. The method typically outperforms the considered competitors.

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