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本文引用的文献

1
GN-SCCA: GraphNet based Sparse Canonical Correlation Analysis for Brain Imaging Genetics.GN-SCCA:用于脑成像遗传学的基于GraphNet的稀疏典型相关分析
Brain Inform Health (2015). 2015;9250:275-284. doi: 10.1007/978-3-319-23344-4_27.
2
A novel structure-aware sparse learning algorithm for brain imaging genetics.一种用于脑成像遗传学的新型结构感知稀疏学习算法。
Med Image Comput Comput Assist Interv. 2014;17(Pt 3):329-36. doi: 10.1007/978-3-319-10443-0_42.
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Transcriptome-guided amyloid imaging genetic analysis via a novel structured sparse learning algorithm.通过一种新型结构化稀疏学习算法进行转录组引导的淀粉样蛋白成像遗传分析。
Bioinformatics. 2014 Sep 1;30(17):i564-71. doi: 10.1093/bioinformatics/btu465.
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Correspondence between fMRI and SNP data by group sparse canonical correlation analysis.通过组稀疏典型相关分析实现功能磁共振成像(fMRI)数据与单核苷酸多态性(SNP)数据之间的对应关系。
Med Image Anal. 2014 Aug;18(6):891-902. doi: 10.1016/j.media.2013.10.010. Epub 2013 Oct 31.
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Feature Grouping and Selection Over an Undirected Graph.无向图上的特征分组与选择
KDD. 2012:922-930. doi: 10.1145/2339530.2339675.
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Segmentation and volumetric analysis of the caudate nucleus in Alzheimer's disease.阿尔茨海默病尾状核的分割和体积分析。
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APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study.载脂蛋白E(APOE)和丁酰胆碱酯酶(BCHE)作为脑淀粉样蛋白沉积的调节因子:一项氟代硼吡咯正电子发射断层扫描全基因组关联研究。
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Interpretable whole-brain prediction analysis with GraphNet.基于 GraphNet 的可解释全脑预测分析。
Neuroimage. 2013 May 15;72:304-21. doi: 10.1016/j.neuroimage.2012.12.062. Epub 2013 Jan 5.
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Structure-constrained sparse canonical correlation analysis with an application to microbiome data analysis.基于结构约束的稀疏典型相关分析及其在微生物组数据分析中的应用。
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Discovering genetic associations with high-dimensional neuroimaging phenotypes: A sparse reduced-rank regression approach.发现与高维神经影像学表型相关的遗传关联:稀疏降秩回归方法。
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用于脑成像遗传学的结构化稀疏典型相关分析:一种改进的GraphNet方法。

Structured sparse canonical correlation analysis for brain imaging genetics: an improved GraphNet method.

作者信息

Du Lei, Huang Heng, Yan Jingwen, Kim Sungeun, Risacher Shannon L, Inlow Mark, Moore Jason H, Saykin Andrew J, Shen Li

机构信息

Department of Radiology and Imaging Sciences, Indiana University, Indianapolis, IN, USA.

Department of Computer Science & Engineering, The University of Texas at Arlington, Arlington, TX, USA.

出版信息

Bioinformatics. 2016 May 15;32(10):1544-51. doi: 10.1093/bioinformatics/btw033. Epub 2016 Jan 21.

DOI:10.1093/bioinformatics/btw033
PMID:26801960
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4907375/
Abstract

MOTIVATION

Structured sparse canonical correlation analysis (SCCA) models have been used to identify imaging genetic associations. These models either use group lasso or graph-guided fused lasso to conduct feature selection and feature grouping simultaneously. The group lasso based methods require prior knowledge to define the groups, which limits the capability when prior knowledge is incomplete or unavailable. The graph-guided methods overcome this drawback by using the sample correlation to define the constraint. However, they are sensitive to the sign of the sample correlation, which could introduce undesirable bias if the sign is wrongly estimated.

RESULTS

We introduce a novel SCCA model with a new penalty, and develop an efficient optimization algorithm. Our method has a strong upper bound for the grouping effect for both positively and negatively correlated features. We show that our method performs better than or equally to three competing SCCA models on both synthetic and real data. In particular, our method identifies stronger canonical correlations and better canonical loading patterns, showing its promise for revealing interesting imaging genetic associations.

AVAILABILITY AND IMPLEMENTATION

The Matlab code and sample data are freely available at http://www.iu.edu/∼shenlab/tools/angscca/

CONTACT

shenli@iu.edu

SUPPLEMENTARY INFORMATION

Supplementary data are available at Bioinformatics online.

摘要

动机

结构化稀疏典型相关分析(SCCA)模型已被用于识别影像遗传学关联。这些模型要么使用组套索,要么使用图引导融合套索来同时进行特征选择和特征分组。基于组套索的方法需要先验知识来定义组,这在缺乏或没有完整先验知识时限制了其能力。图引导方法通过使用样本相关性来定义约束克服了这一缺点。然而,它们对样本相关性的符号敏感,如果符号估计错误,可能会引入不良偏差。

结果

我们引入了一种带有新惩罚项的新型SCCA模型,并开发了一种高效的优化算法。我们的方法对于正相关和负相关特征的分组效果都有很强的上限。我们表明,在合成数据和真实数据上,我们的方法比三种竞争的SCCA模型表现更好或相当。特别是,我们的方法识别出更强的典型相关性和更好的典型载荷模式,显示出其在揭示有趣的影像遗传学关联方面的前景。

可用性与实现

Matlab代码和样本数据可在http://www.iu.edu/∼shenlab/tools/angscca/免费获取。

联系方式

shenli@iu.edu

补充信息

补充数据可在《生物信息学》在线获取。