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Tobacco Smoking Induced Lung Cancer Prediction By LC-MicroRNAs Secondary Structure Prediction And Target Comparison

机译:烟草吸烟诱导肺癌预测LC-MicroRNA二次结构预测和目标比较

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Cancer is deadly, a genetic disorder in which invoke uncontrolled growth of living cells in a particular region. Cancer is usually invoked by many natural causes like exposure to UV rays, smoking tobacco, oil fogs, and exposure to radioactive frequencies. In this work, we concentrate on tobacco-induced lung cancer. There are many existing systems to detect lung cancer. But none are efficient enough to prevent it before it spreads. In this work, we propose an efficient tool to analyze the possibility of getting affected by Non-Small Cell Lung Cancer (NSCLC) by comparing Lung Cancer microRNAs (LC-miRNAs) structures. Here we use global optimal alignment and TargetScan for target comparison and binding location detection. A previous research showed that major lung cancer genes are targeted by 8 type miRNAs. These 8 LC-miRNAs (let-7a-l, miR-7-1, miR-17, miR-21, miR-96, miR-125a-5p, miR-128b, and miR-145) were used for this analysis for accuracy in research. From this work, we concluded that use of computational techniques in miRNA and sequence analysis can reduce the cost of research and increase the accuracy.
机译:癌症是致命的,一种遗传性疾病,其中调用特定区域中的活细胞的不受控制的生长。通常通过暴露于紫外线,吸烟烟草,油雾和暴露于放射性频率的许多自然原因来调用癌症。在这项工作中,我们专注于烟草诱导的肺癌。有许多现有的系统来检测肺癌。但没有足够有效以防止它在传播之前。在这项工作中,我们提出了一种有效的工具来分析通过比较肺癌微小RNA(LC-MIRNA)结构而受到非小细胞肺癌(NSCLC)影响的可能性。在这里,我们使用全局最佳对准和目标扫描来实现目标比较和绑定位置检测。先前的研究表明,主要肺癌基因靶向8型miRNA。这些8 LC-miRNA(Let-7a-L,miR-7-1,miR-17,miR-21,miR-96,miR-125a-5p,miR-128b和miR-145)用于该分析用于研究的准确性。从这项工作来看,我们得出结论,使用MiRNA和序列分析中的计算技术可以降低研究成本并提高准确性。

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