Building generalized linear models with ultrahigh dimensional features: A sequentially conditional approach.

Building generalized linear models with ultrahigh dimensional features: A sequentially conditional approach.
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构建具有超高维特征的广义线性模型:顺序条件方法。

DOI:
10.1111/biom.13122
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发表时间:
2020
期刊:
影响因子:
1.9
通讯作者:
Li,Yi
Li,Yi
中科院分区:
数学3区
文献类型:
--
作者:
Zheng,Qi;Hong,HyokyoungG;Li,Yi

文献摘要

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条件筛选方法已经成为常用的边缘筛选的一种强有力的替代方法,因为它们可以识别边缘弱但有条件重要的变量。然而,大多数现有的条件筛选方法需要固定的初始条件集,这可能会决定最终选择的变量。如果没有正确选择条件集,则这些方法可能会产生假阴性和假阳性。此外,筛选方法通常需要涉及调整参数和额外的建模步骤,以达到最终模型。我们提出了一个连续的条件处理方法,通过动态更新的条件集与迭代选择过程。我们在广义线性模型的框架下给出了它的理论性质。该方法采用扩展的贝叶斯信息准则作为停止规则,无需选择调整参数或阈值参数即可得到最终模型。通过对基于多发性骨髓瘤患者的基因组谱预测其对治疗的反应的真实的临床研究的广泛模拟和分析,检查所提出的方法的实际效用。
Conditional screening approaches have emerged as a powerful alternative to the commonly used marginal screening, as they can identify marginally weak but conditionally important variables. However, most existing conditional screening methods need to fix the initial conditioning set, which may determine the ultimately selected variables. If the conditioning set is not properly chosen, the methods may produce false negatives and positives. Moreover, screening approaches typically need to involve tuning parameters and extra modeling steps in order to reach a final model. We propose a sequential conditioning approach by dynamically updating the conditioning set with an iterative selection process. We provide its theoretical properties under the framework of generalized linear models. Powered by an extended Bayesian information criterion as the stopping rule, the method will lead to a final model without the need to choose tuning parameters or threshold parameters. The practical utility of the proposed method is examined via extensive simulations and analysis of a real clinical study on predicting multiple myeloma patients’ response to treatment based on their genomic profiles.