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Improved quality control processing of peptide-centric LC-MS proteomics data

机译:改进的以肽为中心的LC-MS蛋白质组学数据的质量控制处理

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摘要

Motivation: In the analysis of differential peptide peak intensities (i.e. abundance measures), LC-MS analyses with poor quality peptide abundance data can bias downstream statistical analyses and hence the biological interpretation for an otherwise high-quality dataset. Although considerable effort has been placed on assuring the quality of the peptide identification with respect to spectral processing, to date quality assessment of the subsequent peptide abundance data matrix has been limited to a subjective visual inspection of run-by-run correlation or individual peptide components. Identifying statistical outliers is a critical step in the processing of proteomics data as many of the downstream statistical analyses [e.g. analysis of variance (ANOVA)] rely upon accurate estimates of sample variance, and their results are influenced by extreme values.
机译:动机:在分析差异化肽峰强度(即丰度测量)时,使用质量较差的肽丰度数据进行的LC-MS分析可能会使下游的统计分析产生偏差,从而对原本高质量的数据集进行生物学解释。尽管已投入大量精力来确保肽段鉴定在光谱处理方面的质量,但迄今为止,后续肽丰度数据矩阵的质量评估仅限于主观目视检查逐次运行相关性或单个肽组分。与许多下游统计分析一样,识别蛋白质组统计数据是蛋白质组学数据处理中的关键步骤。方差分析(ANOVA)]依赖于样本方差的准确估计,其结果受极值影响。

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