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分类依据与纠错

AI 根据所提供的论文材料归类:摘要直接研究潜在因果变量及跨模态因果关系的可识别性。

反馈分类问题

Causal Representation Learning from Multimodal Biomedical Observations

从多模态生物医学观测中学习因果表征

正在核对关联版本…

代码、数据与补充材料

正在核对对应版本的资源…

关注这篇论文的作者
Yuewen Sun
Lingjing Kong
Guangyi Chen
Loka Li
Gongxu Luo
Zijian Li
Yixuan Zhang
Yujia Zheng
Mengyue Yang
Petar Stojanov
Eran Segal
Eric P. Xing
Kun Zhang

从多模态生物医学观测中学习因果表征

研究问题
如何从多模态生物医学观测中识别可解释的潜在因果变量,并在减少参数限制的同时,将识别精度推进到各个潜在分量?
方法与思路
作者采用允许跨模态因果关系的非参数潜在分布,以模态之间因果连接的结构稀疏性建立识别结果,并给出实现框架。
材料陈述的贡献
摘要称,识别保证由既有子空间层面扩展到各潜在分量;数值、合成及真实人类表型实验用于展示框架的可行性与解释性。
阅读关注点
应核对结构稀疏性的精确定义、观测与潜变量之间的模型条件,以及分量识别允许的变换;再查看真实数据解释如何得到验证。
阅读边界
这是 arXiv 预印本,不能据此确认同行评审或期刊接收;摘要未说明完整识别条件,与既有生物医学研究一致也不足以确认因果机制。

原文摘要

Prevalent in biomedical applications (e.g., human phenotype research), multimodal datasets can provide valuable insights into the underlying physiological mechanisms. However, current machine learning (ML) models designed to analyze these datasets often lack interpretability and identifiability guarantees, which are essential for biomedical research. Recent advances in causal representation learning have shown promise in identifying interpretable latent causal variables with formal theoretical guarantees. Unfortunately, most current work on multimodal distributions either relies on restrictive parametric assumptions or yields only coarse identification results, limiting their applicability to biomedical research that favors a detailed understanding of the mechanisms. In this work, we aim to develop flexible identification conditions for multimodal data and principled methods to facilitate the understanding of biomedical datasets. Theoretically, we consider a nonparametric latent distribution (c.f., parametric assumptions in previous work) that allows for causal relationships across potentially different modalities. We establish identifiability guarantees for each latent component, extending the subspace identification results from previous work. Our key theoretical contribution is the structural sparsity of causal connections between modalities, which, as we will discuss, is natural for a large collection of biomedical systems. Empirically, we present a practical framework to instantiate our theoretical insights. We demonstrate the effectiveness of our approach through extensive experiments on both numerical and synthetic datasets. Results on a real-world human phenotype dataset are consistent with established biomedical research, validating our theoretical and methodological framework.

笔记与分组