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{"title":"Leveraging Experimental Details for an Improved Understanding of Host-Pathogen Interactome","authors":"Mais Ammari, Fiona McCarthy, Bindu Nanduri","doi":"10.1002/cpbi.44","DOIUrl":null,"url":null,"abstract":"<p>An increasing proportion of curated host-pathogen interaction (HPI) information is becoming available in interaction databases. These data represent detailed, experimentally-verified, molecular interaction data, which may be used to better understand infectious diseases. By their very nature, HPIs are context dependent, where the outcome of two proteins as interacting or not depends on the precise biological conditions studied and approaches used for identifying these interactions. The associated biology and the technical details of the experiments identifying interacting protein molecules are increasing being curated using defined curation standards but are overlooked in current HPI network modeling. Given the increase in data size and complexity, awareness of the process and variables included in HPI identification and curation, and their effect on data analysis and interpretation is crucial in understanding pathogenesis. We describe the use of HPI data for network modeling, aspects of curation that can help researchers to more accurately model specific infection conditions, and provide examples to illustrate these principles. © 2018 by John Wiley & Sons, Inc.</p>","PeriodicalId":10958,"journal":{"name":"Current protocols in bioinformatics","volume":"61 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpbi.44","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current protocols in bioinformatics","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpbi.44","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
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Abstract
An increasing proportion of curated host-pathogen interaction (HPI) information is becoming available in interaction databases. These data represent detailed, experimentally-verified, molecular interaction data, which may be used to better understand infectious diseases. By their very nature, HPIs are context dependent, where the outcome of two proteins as interacting or not depends on the precise biological conditions studied and approaches used for identifying these interactions. The associated biology and the technical details of the experiments identifying interacting protein molecules are increasing being curated using defined curation standards but are overlooked in current HPI network modeling. Given the increase in data size and complexity, awareness of the process and variables included in HPI identification and curation, and their effect on data analysis and interpretation is crucial in understanding pathogenesis. We describe the use of HPI data for network modeling, aspects of curation that can help researchers to more accurately model specific infection conditions, and provide examples to illustrate these principles. © 2018 by John Wiley & Sons, Inc.
利用实验细节来提高对宿主-病原体相互作用组的理解
越来越多的宿主-病原体相互作用(HPI)信息在相互作用数据库中可用。这些数据代表了详细的、经过实验验证的分子相互作用数据,可用于更好地了解传染病。就其本质而言,hpi依赖于上下文,其中两个蛋白质相互作用的结果取决于所研究的精确生物学条件和用于识别这些相互作用的方法。相关的生物学和鉴定相互作用蛋白质分子的实验的技术细节正在越来越多地使用定义的管理标准进行管理,但在当前的HPI网络建模中被忽视。鉴于数据量和复杂性的增加,了解HPI识别和管理中的过程和变量及其对数据分析和解释的影响对于理解发病机制至关重要。我们描述了HPI数据在网络建模中的使用,以及可以帮助研究人员更准确地建立特定感染条件模型的管理方面,并提供了示例来说明这些原则。©2018 by John Wiley &儿子,Inc。
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