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用于多个遗传数据集的惩罚积分半参数交互分析。

Penalized integrative semiparametric interaction analysis for multiple genetic datasets.

机构信息

Center for Applied Statistics, Renmin University of China, Beijing, China.

School of Statistics, Renmin University of China, Beijing, China.

出版信息

Stat Med. 2019 Jul 30;38(17):3221-3242. doi: 10.1002/sim.8172. Epub 2019 Apr 16.

DOI:10.1002/sim.8172
PMID:30993736
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6606355/
Abstract

In this article, we consider a semiparametric additive partially linear interaction model for the integrative analysis of multiple genetic datasets. The goals are to identify important genetic predictors and gene-gene interactions and to estimate the nonparametric functions that describe the environmental effects at the same time. To find the similarities and differences of the genetic effects across different datasets, we impose a group structure on the regression coefficients matrix under the homogeneity assumption, ie, models for different datasets share the same sparsity structure, but the coefficients may differ across datasets. We develop an iterative approach to estimate the parameters of main effects, interactions and nonparametric functions, where a reparametrization of interaction parameters is implemented to meet the strong hierarchy assumption. We demonstrate the advantages of the proposed method in identification, estimation, and prediction in a series of numerical studies. We also apply the proposed method to the Skin Cutaneous Melanoma data and the lung cancer data from the Cancer Genome Atlas.

摘要

在本文中,我们考虑了一种用于综合分析多个遗传数据集的半参数加性部分线性交互模型。目的是识别重要的遗传预测因子和基因-基因相互作用,并同时估计描述环境效应的非参数函数。为了找到不同数据集之间遗传效应的相似性和差异,我们在同质性假设下对回归系数矩阵施加了一个群组结构,即不同数据集的模型共享相同的稀疏结构,但系数可能在数据集之间有所不同。我们开发了一种迭代方法来估计主要效应、交互作用和非参数函数的参数,其中实施了交互作用参数的重参数化,以满足强层次假设。我们在一系列数值研究中展示了所提出方法在识别、估计和预测方面的优势。我们还将所提出的方法应用于来自癌症基因组图谱的皮肤黑色素瘤数据和肺癌数据。

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本文引用的文献

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Identification of cancer omics commonality and difference via community fusion.通过社区融合来识别癌症组学的共性和差异。
Stat Med. 2019 Mar 30;38(7):1200-1212. doi: 10.1002/sim.8027. Epub 2018 Nov 12.
2
Promoting Similarity of Sparsity Structures in Integrative Analysis with Penalization.在惩罚性整合分析中促进稀疏结构的相似性
J Am Stat Assoc. 2017;112(517):342-350. doi: 10.1080/01621459.2016.1139497. Epub 2017 May 3.
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Additive varying-coefficient model for nonlinear gene-environment interactions.用于非线性基因-环境相互作用的加性变系数模型。
Stat Appl Genet Mol Biol. 2018 Feb 8;17(2):sagmb-2017-0008. doi: 10.1515/sagmb-2017-0008.
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Identifying gene-gene interactions using penalized tensor regression.使用惩罚张量回归识别基因-基因相互作用。
Stat Med. 2018 Feb 20;37(4):598-610. doi: 10.1002/sim.7523. Epub 2017 Oct 16.
5
Bioinformatics analyses of the differences between lung adenocarcinoma and squamous cell carcinoma using The Cancer Genome Atlas expression data.利用癌症基因组图谱表达数据对肺腺癌和肺鳞状细胞癌之间差异的生物信息学分析。
Mol Med Rep. 2017 Jul;16(1):609-616. doi: 10.3892/mmr.2017.6629. Epub 2017 May 25.
6
Promoting similarity of model sparsity structures in integrative analysis of cancer genetic data.在癌症遗传数据的综合分析中促进模型稀疏结构的相似性。
Stat Med. 2017 Feb 10;36(3):509-559. doi: 10.1002/sim.7138. Epub 2016 Sep 25.
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Computational Identification of Novel Stage-Specific Biomarkers in Colorectal Cancer Progression.结直肠癌进展过程中新型阶段特异性生物标志物的计算识别
PLoS One. 2016 May 31;11(5):e0156665. doi: 10.1371/journal.pone.0156665. eCollection 2016.
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A common promoter hypomethylation signature in invasive breast, liver and prostate cancer cell lines reveals novel targets involved in cancer invasiveness.侵袭性乳腺癌、肝癌和前列腺癌细胞系中常见的启动子低甲基化特征揭示了参与癌症侵袭的新靶点。
Oncotarget. 2015 Oct 20;6(32):33253-68. doi: 10.18632/oncotarget.5291.
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A LASSO FOR HIERARCHICAL INTERACTIONS.用于分层交互的套索法
Ann Stat. 2013 Jun;41(3):1111-1141. doi: 10.1214/13-AOS1096.
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A penalized robust semiparametric approach for gene-environment interactions.一种用于基因-环境相互作用的惩罚稳健半参数方法。
Stat Med. 2015 Dec 30;34(30):4016-30. doi: 10.1002/sim.6609. Epub 2015 Aug 3.