Imputation of missing values in lipidomic datasets

IF 3.4 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Proteomics Pub Date : 2024-04-11 DOI:10.1002/pmic.202300606
Nicolas Frölich, Christian Klose, Elisabeth Widén, Samuli Ripatti, Mathias J. Gerl
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引用次数: 0

Abstract

Lipidomic data often exhibit missing data points, which can be categorized as missing completely at random (MCAR), missing at random, or missing not at random (MNAR). In order to utilize statistical methods that require complete datasets or to improve the identification of potential effects in statistical comparisons, imputation techniques can be employed. In this study, we investigate commonly used methods such as zero, half-minimum, mean, and median imputation, as well as more advanced techniques such as k-nearest neighbor and random forest imputation. We employ a combination of simulation-based approaches and application to real datasets to assess the performance and effectiveness of these methods. Shotgun lipidomics datasets exhibit high correlations and missing values, often due to low analyte abundance, characterized as MNAR. In this context, k-nearest neighbor approaches based on correlation and truncated normal distributions demonstrate best performance. Importantly, both methods can effectively impute missing values independent of the type of missingness, the determination of which is nearly impossible in practice. The imputation methods still control the type I error rate.

Abstract Image

脂质体数据集缺失值的估算
脂质组学数据经常会出现数据点缺失,可分为完全随机缺失(MCAR)、随机缺失或非随机缺失(MNAR)。为了利用需要完整数据集的统计方法,或在统计比较中更好地识别潜在效应,可以采用估算技术。在本研究中,我们研究了常用的方法,如零点、半最小值、平均值和中位数估算,以及更先进的技术,如 k 近邻和随机森林估算。我们将基于模拟的方法与真实数据集的应用相结合,以评估这些方法的性能和有效性。霰弹枪脂质组学数据集表现出高相关性和缺失值,这通常是由于分析物丰度低造成的,被称为 MNAR。在这种情况下,基于相关性和截断正态分布的 k 近邻方法表现出最佳性能。重要的是,这两种方法都能有效地估算缺失值,而不受缺失类型的影响,缺失类型的确定在实践中几乎是不可能的。这些估算方法仍能控制 I 类错误率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Proteomics
Proteomics 生物-生化研究方法
CiteScore
6.30
自引率
5.90%
发文量
193
审稿时长
3 months
期刊介绍: PROTEOMICS is the premier international source for information on all aspects of applications and technologies, including software, in proteomics and other "omics". The journal includes but is not limited to proteomics, genomics, transcriptomics, metabolomics and lipidomics, and systems biology approaches. Papers describing novel applications of proteomics and integration of multi-omics data and approaches are especially welcome.
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