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

机译:利用机器学习算法分析MicroRNA的牛皮癣后转录基因调控

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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)是人类中最常见的间间变异。他们对下一代测序(NGS)作为疾病生物标志物的侵扰,以疾病生物标志物用于使用基因组 - 范围的协会研究进行诊断和/或预后。它们沿着基因组,但主要在非编码区。在这些情况下,SNP可能会影响调节区域,例如启动子,增强剂或MICRRNA(miRNA)结合位点。 MiRNA是短的非编码RNA,估计在转录后水平上调节高达60%的基因表达。众所周知,通过误导基因的表达,它们被许多疾病暗示。新的计算技术允许从RNA-SEQ数据提取更多信息,不仅能够测量基因表达,而且可以在基因组上测量基因组。为了理解和模拟这种类型RNA在疾病表型中的效果,使用位于令人讨要的基因的3'UTR(未转换区域)中的SNP进行机器学习算法,以找到生物标志物并描述作用机制。

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