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ABRF Proteome Informatics Research Group (iPRG) 2016 Study: Inferring Proteoforms from Bottom-up Proteomics Data

机译:ABRF蛋白质组信息学研究小组(iPRG)2016研究:从下而上的蛋白质组学数据推断蛋白质形式

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摘要

This report presents the results from the 2016 Association of Biomolecular Resource Facilities Proteome Informatics Research Group (iPRG) study on proteoform inference and false discovery rate (FDR) estimation from bottom-up proteomics data. For this study, 3 replicate Q Exactive Orbitrap liquid chromatography-tandom mass spectrometry datasets were generated from each of 4 Escherichia coli samples spiked with different equimolar mixtures of small recombinant proteins selected to mimic pairs of homologous proteins. Participants were given raw data and a sequence file and asked to identify the proteins and provide estimates on the FDR at the proteoform level. As part of this study, we tested a new submission system with a format validator running on a virtual private server (VPS) and allowed methods to be provided as executable R Markdown or IPython Notebooks. The task was perceived as difficult, and only eight unique submissions were received, although those who participated did well with no one method performing best on all samples. However, none of the submissions included a complete Markdown or Notebook, even though examples were provided. Future iPRG studies need to be more successful in promoting and encouraging participation. The VPS and submission validator easily scale to much larger numbers of participants in these types of studies. The unique “ground-truth” dataset for proteoform identification generated for this study is now available to the research community, as are the server-side scripts for validating and managing submissions.
机译:本报告介绍了2016年生物分子资源设施蛋白质组信息学研究小组(iPRG)的研究结果,该研究对自下而上的蛋白质组学数据进行的蛋白质形式推断和错误发现率(FDR)估计。对于本研究,从掺有不同等摩尔混合物的小重组蛋白的4个大肠埃希氏菌样品的每一个中生成3个重复的Q Exactive Orbitrap液相色谱-质谱质谱数据集,这些小摩尔重组蛋白被选择来模拟成对的同源蛋白。为参与者提供了原始数据和序列文件,并要求他们鉴定蛋白质并在蛋白形式水平上对FDR进行估算。作为这项研究的一部分,我们测试了一个新的提交系统,该系统具有在虚拟专用服务器(VPS)上运行的格式验证器,并允许将这些方法作为可执行文件R Markdown或IPython Notebooks提供。这项任务被认为是困难的,尽管只有那些参加的人表现出色,但没有一种方法在所有样本上都能表现出最佳的表现,因此只收到了八份独特的论文。但是,即使提供了示例,也没有一个完整的Markdown或Notebook。未来的iPRG研究需要更成功地促进和鼓励参与。 VPS和提交验证器很容易扩展为这些类型研究中的大量参与者。现在,研究团体可以使用此研究生成的独特的“真相”数据集来进行蛋白形式鉴定,以及用于验证和管理提交的服务器端脚本。

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