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RDDpred: a condition-specific RNA-editing prediction model from RNA-seq data

机译:RDDPRED:来自RNA-SEQ数据的条件特定的RNA编辑预测模型

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Background: RNA-editing is an important post-transcriptional RNA sequence modification performed by two catalytic enzymes, "ADAR"(A-to-l) and "APOBEC'(C-to-U). By utilizing high-throughput sequencing technologies, the biological function of RNA-editing has been actively investigated. Currently, RNA-editing is considered to be a key regulator that controls various cellular functions, such as protein activity, alternative splicing pattern of mRNA, and substitution of miRNA targeting site. DARNED, a public RDD database, reported that there are more than 300-thousands RNA-editing sites detected in human genome(hg19). Moreover, multiple studies suggested that RNA-editing events occur in highly specific conditions. According to DARNED, 97.62 % of registered editing sites were detected in a single tissue or in a specific condition, which also supports that the RNA-editing events occur condition-specifically. Since RNA-seq can capture the whole landscape of transcriptome, RNA-seq is widely used for RDD prediction. However, significant amounts of false positives or artefacts can be generated when detecting RNA-editing from RNA-seq. Since it is difficult to perform experimental validation at the whole-transcriptome scale, there should be a powerful computational tool to distinguish true RNA-editing events from artefacts. Result: We developed RDDpred, a Random Forest RDD classifier. RDDpred reports potentially true RNA-editing events from RNA-seq data. RDDpred was tested with two publicly available RNA-editing datasets and successfully reproduced RDDs reported in the two studies (90 %, 95 %) while rejecting false-discoveries (NPV: 75 %, 84 %). Conclusion: RDDpred automatically compiles condition-specific training examples without experimental validations and then construct a RDD classifier. As far as we know, RDDpred is the very first machine-learning based automated pipeline for RDD prediction. We believe that RDDpred will be very useful and can contribute significantly to the stud> of condition-specificRNA-editing. RDDpred is available at http: //biohealth. snu. ac . kr/software/ RDDpred.
机译:背景:RNA编辑是由两种催化酶“ADAR”(A-TO-L)和“Apobec”(C-TO-U)进行的重要转录后RNA序列改性。通过利用高通量测序技术, RNA编辑的生物学功能已被主动研究。目前,RNA编辑被认为是控制各种细胞功能的关键调节剂,例如蛋白质活性,mRNA的替代剪接模式,以及miRNA靶向部位的替代。DARNED,公共RDD数据库报道,在人类基因组(HG19)中存在超过300万次RNA编辑位点。此外,多种研究表明RNA编辑事件发生在高度特定的条件下。根据Darned,97.62%的注册在单个组织中或特定条件下检测到编辑部位,这也支持RNA编辑事件发生条件 - 特别是。由于RNA-SEQ可以捕获转录组的整体景观,因此RNA-SEQ广泛使用D对于RDD预测。然而,在检测来自RNA-SEQ的RNA编辑时,可以产生大量的误阳性或人工制品。由于难以以整个转录组规模执行实验验证,因此应该有一个强大的计算工具,以区分真实的RNA编辑事件。结果:我们开发了一个随机森林RDD分类器的RDDPRED。 RDDPRED从RNA-SEQ数据报告可能的真正的RNA编辑事件。 RDDPRED用两种公开的RNA编辑数据集进行了测试,并成功再现了两项研究中报告的RDD(90%,95%),同时拒绝虚假发现(NPV:75%,84%)。结论:RDDPRED在没有实验验证的情况下自动编译条件特定的培训示例,然后构建RDD分类器。据我们所知,RDDPRED是用于RDD预测的第一个基于机器学习的自动化管道。我们认为,RDDPRED将非常有用,可以对病情特定rna编辑的螺柱>显着贡献。 RDDPRED可在HTTP:// BioHealth提供。 Snu。 AC。 KR / Software / RDDPRED。

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