...
首页> 外文期刊>Proteomics >In-depth evaluation of software tools for data-independent acquisition based label-free quantification
【24h】

In-depth evaluation of software tools for data-independent acquisition based label-free quantification

机译:对基于数据独立采集的无标签量化的软件工具进行深入评估

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Label-free quantification (LFQ) based on data-independent acquisition workflows currently experiences increasing popularity. Several software tools have been recently published or are commercially available. The present study focuses on the evaluation of three different software packages (Progenesis, synapter, and ISOQuant) supporting ion mobility enhanced data-independent acquisition data. In order to benchmark the LFQ performance of the different tools, we generated two hybrid proteome samples of defined quantitative composition containing tryptically digested proteomes of three different species (mouse, yeast, Escherichia coli). This model dataset simulates complex biological samples containing large numbers of both unregulated (background) proteins as well as up- and downregulated proteins with exactly known ratios between samples. We determined the number and dynamic range of quantifiable proteins and analyzed the influence of applied algorithms (retention time alignment, clustering, normalization, etc.) on quantification results. Analysis of technical reproducibility revealed median coefficients of variation of reported protein abundances below 5% for MS' data for Progenesis and I SOQuant. Regarding accuracy of LFQ, evaluation with synapter and IS OQuant yielded superior results compared to Progenesis. In addition, we discuss reporting formats and user friendliness of the software packages. The data generated in this study have been deposited to the ProteomeXchange Consortium with identifier PXDO01240 (http://proteomecentral.proteomexchange.org/dataset/PXDO01240).
机译:基于数据无关的采集工作流程的无标签量化(LFQ)目前经历越来越受欢迎。最近发表了几种软件工具或可商购获得。本研究重点研究了支持离子移动性增强的数据独立采集数据的三种不同软件包(后代,Synapter和IsoQuant)的评估。为了基准不同工具的LFQ性能,我们产生了含有三种不同物种(小鼠,酵母,大肠杆菌)的含有胰蛋白酶消化的蛋白质蛋白蛋白蛋白蛋白蛋白组的两种杂化蛋白质组样本。该模型数据集模拟了包含大量未调节(背景)蛋白的复杂生物样品以及具有恰到详细的蛋白质,在样品之间具有恰好已知的比率。我们确定了量化蛋白质的数量和动态范围,并分析了应用算法(保留时间对准,聚类,归一化,归一化等)对定量结果的影响。技术再现性分析显示,对于MS'数据进行后,报告的蛋白质丰度的变异的中值系数和我的致致牙齿。关于LFQ的准确性,用SYNATER评估并且臭壳的评估产生了优异的结果与后置。此外,我们讨论了软件包的报告格式和用户友好性。本研究中生成的数据已寄存在具有标识符PXDO01240(http://proteomecentral.proteomexchange.org/dataset/pxdo01240)的ProteomexChange联盟。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号