SGTCDA:通过可解释的图形转换器和有效评估来预测 circRNA 与药物敏感性之间的关联。

IF 3.5 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Hongwei Xia, Caiyue Dong, Xinxing Chen, Zhuoyu Wei, Lichuan Gu, Xiaolei Zhu
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引用次数: 0

摘要

CircRNAs 是一种环状非编码 RNA,最近的研究证明了其与药物敏感性的关联。由于检测 circRNA 与药物敏感性之间关系的生物医学实验成本高昂,人们开发了几种计算方法。然而,这些方法主要基于五倍或十倍交叉验证进行评估,往往过于乐观。此外,这些模型还存在技术问题,如过度平滑和过度扭曲。为了解决这些问题,我们提出了一种基于独立测试集的关联预测相关研究模型评估策略。在这种有效评估的基础上,我们通过整合结构深度网络嵌入(SDNE)和图转换器构建了一个模型--SGTCDA,用于预测circRNA-药物敏感性的潜在关联,该模型能有效捕捉节点的长程依赖关系和局部结构信息。我们在训练集和独立测试集上的结果表明,SGTCDA 的表现优于其他最先进的模型,证明了它在准确预测 circRNA-药物敏感性方面的能力。此外,我们还利用 EdgeSHAPer 解释了所提出的 SGTCDA 模型的性能,这说明药物之间的边缘比其他边缘对该模型的性能更为重要。SGTCDA 的源代码和数据集可在以下网址获取:https://github.com/hwxia/SGTCDA 。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SGTCDA: Prediction of circRNA-drug sensitivity associations with interpretable graph transformers and effective assessment.

CircRNAs are a type of circular non-coding RNA whose associations with drug sensitivities have been demonstrated in recent studies. Due to the high cost of biomedical experiments for detecting the associations between circRNAs and drug sensitivities, several computational methods have been developed. However, these methods were evaluated mainly based on 5- or tenfold cross-validation, which are often over-optimistic. Furthermore, there are technique issues with these models, such as over-smoothing and over-squashing. To address these issues, we propose a strategy to evaluate models based on independent test sets for association prediction-related studies. In the light of this effective assessment, we constructed a model, SGTCDA, by integrating structural deep network embedding (SDNE) and a graph transformer to predict the potential associations of circRNA-drug sensitivity, which can efficiently capture long-range dependencies and local structural information of nodes. Our results on the training sets and the independent test sets indicate that SGTCDA outperforms the other state-of-the-art models, demonstrating its capacity for accurate prediction of circRNA-drug sensitivity. Moreover, we leveraged EdgeSHAPer to explain the performance of the proposed SGTCDA model, which illustrates that the edges between drugs are more important than other edges for the performance of the model. The source code and dataset of SGTCDA are available at: https://github.com/hwxia/SGTCDA .

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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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