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Using a spike-in experiment to evaluate analysis of LC-MS data

机译:使用加标实验评估LC-MS数据分析

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Background Recent advances in liquid chromatography-mass spectrometry (LC-MS) technology have led to more effective approaches for measuring changes in peptide/protein abundances in biological samples. Label-free LC-MS methods have been used for extraction of quantitative information and for detection of differentially abundant peptides/proteins. However, difference detection by analysis of data derived from label-free LC-MS methods requires various preprocessing steps including filtering, baseline correction, peak detection, alignment, and normalization. Although several specialized tools have been developed to analyze LC-MS data, determining the most appropriate computational pipeline remains challenging partly due to lack of established gold standards. Results The work in this paper is an initial study to develop a simple model with "presence" or "absence" condition using spike-in experiments and to be able to identify these "true differences" using available software tools. In addition to the preprocessing pipelines, choosing appropriate statistical tests and determining critical values are important. We observe that individual statistical tests could lead to different results due to different assumptions and employed metrics. It is therefore preferable to incorporate several statistical tests for either exploration or confirmation purpose. Conclusions The LC-MS data from our spike-in experiment can be used for developing and optimizing LC-MS data preprocessing algorithms and to evaluate workflows implemented in existing software tools. Our current work is a stepping stone towards optimizing LC-MS data acquisition and testing the accuracy and validity of computational tools for difference detection in future studies that will be focused on spiking peptides of diverse physicochemical properties in different concentrations to better represent biomarker discovery of differentially abundant peptides/proteins.
机译:背景技术液相色谱-质谱(LC-MS)技术的最新进展已导致测量生物样品中肽/蛋白质丰度变化的更有效方法。无标记的LC-MS方法已用于提取定量信息和检测差异丰富的肽/蛋白质。但是,通过分析源自无标记LC-MS方法的数据进行差异检测需要各种预处理步骤,包括过滤,基线校正,峰检测,比对和归一化。尽管已经开发了几种专用工具来分析LC-MS数据,但由于缺乏既定的金标准,因此确定最合适的计算管道仍然面临挑战。结果本文的工作是一项初步研究,目的是使用插入实验开发具有“存在”或“不存在”条件的简单模型,并能够使用可用的软件工具识别这些“真实差异”。除了预处理管道外,选择适当的统计测试和确定关键值也很重要。我们观察到,由于不同的假设和采用的指标,单个统计测试可能导致不同的结果。因此,出于探索或确认目的,最好合并几个统计检验。结论来自我们的加标实验的LC-MS数据可用于开发和优化LC-MS数据预处理算法,以及评估现有软件工具中实现的工作流程。我们目前的工作是朝着优化LC-MS数据采集和测试用于差异检测的计算工具的准确性和有效性打下基础,在未来的研究中,该研究将集中于掺入不同浓度的各种理化性质的肽,以更好地代表差异化生物标志物的发现。丰富的肽/蛋白质。

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