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Machine Learning SNP Based Prediction for Precision Medicine

机译:基于机器学习SNP的精准医学预测

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In the past decade, precision genomics based medicine has emerged to provide tailored and effective healthcare for patients depending upon their genetic features. Genome Wide Association Studies have also identified population based risk genetic variants for common and complex diseases. In order to meet the full promise of precision medicine, research is attempting to leverage our increasing genomic understanding and further develop personalized medical healthcare through ever more accurate disease risk prediction models. Polygenic risk scoring and machine learning are two primary approaches for disease risk prediction. Despite recent improvements, the results of polygenic risk scoring remain limited due to the approaches that are currently used. By contrast, machine learning algorithms have increased predictive abilities for complex disease risk. This increase in predictive abilities results from the ability of machine learning algorithms to handle multi-dimensional data. Here, we provide an overview of polygenic risk scoring and machine learning in complex disease risk prediction. We highlight recent machine learning application developments and describe how machine learning approaches can lead to improved complex disease prediction, which will help to incorporate genetic features into future personalized healthcare. Finally, we discuss how the future application of machine learning prediction models might help manage complex disease by providing tissue-specific targets for customized, preventive interventions.
机译:在过去的十年中,基于精确基因组学的医学已经出现,可以根据患者的遗传特征为他们提供量身定制的有效医疗保健。全基因组关联研究还确定了常见和复杂疾病的基于人群的风险遗传变异。为了满足精准医学的全部希望,研究正在尝试利用我们不断增长的基因组理解,并通过更加准确的疾病风险预测模型进一步开发个性化的医疗保健。多基因风险评分和机器学习是疾病风险预测的两种主要方法。尽管最近有所改进,但由于当前使用的方法,多基因风险评分的结果仍然有限。相比之下,机器学习算法对复杂疾病风险的预测能力有所提高。预测能力的提高源于机器学习算法处理多维数据的能力。在这里,我们概述了复杂疾病风险预测中的多基因风险评分和机器学习。我们重点介绍了机器学习应用程序的最新发展,并描述了机器学习方法如何改善复杂疾病的预测,这将有助于将遗传特征整合到未来的个性化医疗中。最后,我们讨论了机器学习预测模型的未来应用如何通过为定制的预防性干预提供组织特定的目标来帮助管理复杂疾病。

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