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The CAFA challenge reports improved protein function prediction and new functional annotations for hundreds of genes through experimental screens

机译:CAFA挑战通过实验筛网报告了数百个基因的改善的蛋白质功能预测和新的功能注释

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Abstract BackgroundThe Critical Assessment of Functional Annotation (CAFA) is an ongoing, global, community-driven effort to evaluate and improve the computational annotation of protein function.ResultsHere, we report on the results of the third CAFA challenge, CAFA3, that featured an expanded analysis over the previous CAFA rounds, both in terms of volume of data analyzed and the types of analysis performed. In a novel and major new development, computational predictions and assessment goals drove some of the experimental assays, resulting in new functional annotations for more than 1000 genes. Specifically, we performed experimental whole-genome mutation screening in Candida albicans and Pseudomonas aureginosa genomes, which provided us with genome-wide experimental data for genes associated with biofilm formation and motility. We further performed targeted assays on selected genes in Drosophila melanogaster , which we suspected of being involved in long-term memory.ConclusionWe conclude that while predictions of the molecular function and biological process annotations have slightly improved over time, those of the cellular component have not. Term-centric prediction of experimental annotations remains equally challenging; although the performance of the top methods is significantly better than the expectations set by baseline methods in C. albicans and D. melanogaster , it leaves considerable room and need for improvement. Finally, we report that the CAFA community now involves a broad range of participants with expertise in bioinformatics, biological experimentation, biocuration, and bio-ontologies, working together to improve functional annotation, computational function prediction, and our ability to manage big data in the era of large experimental screens.
机译:摘要背景技术功能注释(CAFA)的批判性评估是一个持续的,全球,社区驱动的努力,用于评估和改进蛋白质函数的计算注释。评估,我们报告了第三次CAFA挑战的结果CAFA3,其特征在于在分析的数据量和进行的分析类型的数据方面,分析了先前的CAFA轮。在一个新颖的和主要的新发展中,计算预测和评估目标推动了一些实验测定,导致了超过1000个基因的新功能注释。具体而言,我们在念珠菌和假单胞菌Aurepinosa基因组中进行了实验的全基因组突变筛选,该筛选为我们提供了与生物膜形成和运动的基因的基因组实验数据。我们进一步对果蝇Melanogaster的选定基因进行了针对性的测定,我们怀疑涉及长期记忆。结论我们得出结论,虽然分子功能和生物过程注释的预测随着时间的推移略微改善,但细胞组分的含量没有。以实验注释为中心预测仍然同样挑战;虽然顶级方法的性能明显优于C. albicans和D. Melanogaster的基线方法所期望的预期,但它留下了相当大的房间并需要改进。最后,我们报告说,CAFA社区现在涉及具有生物信息学,生物实验,酶和生物本体的专业知识的广泛参与者,共同努力改善功能注释,计算功能预测以及我们管理大数据的能力大型实验屏幕的时代。

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