在代表性不足的人群中改进表型预测的机器学习策略。

David Bonet, May Levin, Daniel Mas Montserrat, Alexander G Ioannidis
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引用次数: 0

摘要

精准医学模型通常对欧洲血统的人群效果更好,这是因为在构建模型的基因组数据集和大规模生物库中,欧洲血统的人群所占比例过高。因此,预测模型可能会误导代表性不足的人群或为其提供不那么准确的治疗建议,从而造成健康差异。本研究介绍了一种可调整的机器学习工具包,该工具包整合了多种现有方法和新技术,以提高基因组数据集中代表性不足人群的预测准确性。通过利用梯度提升和自动化方法等机器学习技术,再加上新颖的人群条件再采样技术,我们的方法显著提高了单核苷酸多态性(SNP)数据对不同人群的表型预测。我们使用英国生物数据库对我们的方法进行了评估,该数据库主要由具有欧洲血统的英国人以及少数具有亚洲和非洲血统的群体组成。性能指标表明,对代表性不足群体的表型预测有了很大改进,预测准确率可与多数群体的预测准确率相媲美。在当前数据集多样性面临挑战的情况下,这种方法在提高预测准确性方面迈出了重要一步。通过整合量身定制的管道,我们的方法促进了统计遗传学方法更公平的有效性和实用性,为更具包容性的模型和结果铺平了道路。
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Machine Learning Strategies for Improved Phenotype Prediction in Underrepresented Populations.

Precision medicine models often perform better for populations of European ancestry due to the over-representation of this group in the genomic datasets and large-scale biobanks from which the models are constructed. As a result, prediction models may misrepresent or provide less accurate treatment recommendations for underrepresented populations, contributing to health disparities. This study introduces an adaptable machine learning toolkit that integrates multiple existing methodologies and novel techniques to enhance the prediction accuracy for underrepresented populations in genomic datasets. By leveraging machine learning techniques, including gradient boosting and automated methods, coupled with novel population-conditional re-sampling techniques, our method significantly improves the phenotypic prediction from single nucleotide polymorphism (SNP) data for diverse populations. We evaluate our approach using the UK Biobank, which is composed primarily of British individuals with European ancestry, and a minority representation of groups with Asian and African ancestry. Performance metrics demonstrate substantial improvements in phenotype prediction for underrepresented groups, achieving prediction accuracy comparable to that of the majority group. This approach represents a significant step towards improving prediction accuracy amidst current dataset diversity challenges. By integrating a tailored pipeline, our approach fosters more equitable validity and utility of statistical genetics methods, paving the way for more inclusive models and outcomes.

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