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评估机器学习方法中分类器特征集在通路空间中距离的方案。

Protocol for assessing distances in pathway space for classifier feature sets from machine learning methods.

作者信息

Tercan Bahar, Apolonio Victor H, Chagas Vinicius S, Wong Christopher K, Lee Jordan A, Yau Christina, Benz Christopher C, Stuart Joshua M, Karlberg Brian J, Ellrott Kyle, Grewal Jasleen K, Jones Steven J M, Zenklusen Jean C, Robertson A Gordon, Laird Peter W, Cherniack Andrew D, Castro Mauro A A

机构信息

Institute of Systems Biology, 401 Terry Avenue North, Seattle, WA 98109, USA.

Bioinformatics and Systems Biology Laboratory, Federal University of Paraná, Curitiba, PR 81520-260, Brazil.

出版信息

STAR Protoc. 2025 Jun 20;6(2):103681. doi: 10.1016/j.xpro.2025.103681. Epub 2025 Mar 18.

DOI:10.1016/j.xpro.2025.103681
PMID:40106435
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11968257/
Abstract

As genes tend to be co-regulated as gene modules, feature selection in machine learning (ML) on gene expression data can be challenged by the complexity of gene regulation. Here, we present a protocol for reconciling differences in classifier features identified using different ML approaches. We describe steps for loading the PathwaySpace R package, preparing input for analysis, and creating density plots of gene sets. We then detail procedures for testing whether apparently distinct feature sets are related in pathway space. For complete details on the use and execution of this protocol, please refer to Ellrott et al..

摘要

由于基因倾向于作为基因模块共同调控,基于基因表达数据的机器学习(ML)中的特征选择可能会受到基因调控复杂性的挑战。在这里,我们提出了一种用于协调使用不同ML方法识别的分类器特征差异的方案。我们描述了加载PathwaySpace R包、准备分析输入以及创建基因集密度图的步骤。然后,我们详细说明了测试明显不同的特征集在通路空间中是否相关的程序。有关此方案的使用和执行的完整详细信息,请参考Ellrott等人的文章。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba49/11968257/86ac1727df80/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba49/11968257/a7b425219fd1/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba49/11968257/8f2a1bc22783/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba49/11968257/86ac1727df80/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba49/11968257/a7b425219fd1/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba49/11968257/8f2a1bc22783/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba49/11968257/86ac1727df80/gr2.jpg

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本文引用的文献

1
Classification of non-TCGA cancer samples to TCGA molecular subtypes using compact feature sets.使用紧凑特征集将非TCGA癌症样本分类为TCGA分子亚型。
Cancer Cell. 2025 Feb 10;43(2):195-212.e11. doi: 10.1016/j.ccell.2024.12.002. Epub 2025 Jan 2.
2
Pathway Commons 2019 Update: integration, analysis and exploration of pathway data.Pathway Commons 2019 更新:途径数据的整合、分析和探索。
Nucleic Acids Res. 2020 Jan 8;48(D1):D489-D497. doi: 10.1093/nar/gkz946.
3
The Molecular Signatures Database (MSigDB) hallmark gene set collection.
分子特征数据库(MSigDB)标志性基因集集合。
Cell Syst. 2015 Dec 23;1(6):417-425. doi: 10.1016/j.cels.2015.12.004.