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Towards an Analysis of Post-Transcriptional Gene Regulation in Psoriasis via microRNAs using Machine Learning Algorithms

机译:使用机器学习算法通过microRNA分析牛皮癣的转录后基因调控

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Single Nucleotide Polymorphisms (SNPs) are the most common inter-individual variations in the human being. They gained popularity with the irruption of Next Generation Sequencing (NGS) as disease biomarkers for diagnosis and/or prognosis using Genome-Wide Association Study. They are along the genome but mostly in the non-coding regions. In these cases, SNPs may affect regulatory regions, such as promoters, enhancers or microRNA (miRNA) binding sites. miRNAs are short non-coding RNAs, that are estimated to regulate up to 60% of gene expression at the post-transcriptional level. It is well known they are implied in many diseases by misregulating the expression of genes. New computational technologies allow extracting more information from RNA-Seq data, being able not only to measure the gene expression but also mapping SNPs on the genome. To understand and model the effects of this type of RNAs in disease phenotype, machine learning algorithms will be trained using SNPs located in the 3'UTR (UnTranslated Region) of deregulated genes to find biomarkers and describe the mechanism of action.
机译:单核苷酸多态性(SNP)是人类中最常见的个体间变异。随着新一代测序(NGS)的使用,它们作为基因组广泛关联研究诊断和/或预后的疾病生物标记物而受到欢迎。它们沿着基因组,但是大部分在非编码区。在这些情况下,SNP可能会影响调控区,例如启动子,增强子或microRNA(miRNA)结合位点。 miRNA是短的非编码RNA,据估计在转录后水平上调节高达60%的基因表达。众所周知,它们通过错误调节基因表达而隐含在许多疾病中。新的计算技术可以从RNA-Seq数据中提取更多信息,不仅可以测量基因表达,还可以在基因组上绘制SNP。为了理解和模拟这种类型的RNA在疾病表型中的作用,将使用位于失调基因的3'UTR(非翻译区)中的SNP训练机器学习算法,以找到生物标记并描述其作用机理。

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