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AI 根据所提供的论文材料归类:摘要聚焦高维生物数据的贝叶斯收缩与变分推断方法,属于计算生物学与统计方法方向,未涉及所提供领域细分中的因果推断、面板、离散选择、时间序列、资产定价等主题,故不选择任何细分。

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BaGGLS: A Bayesian Shrinkage Framework for Interpretable Modeling of Interactions in High-Dimensional Biological Data

BaGGLS:高维生物数据交互可解释建模的贝叶斯收缩框架

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关注这篇论文的作者
Marta S. Lemanczyk
Lucas Kock
Johanna Schlimme
Nadja Klein
Bernhard Y. Renard

BaGGLS:高维生物数据交互可解释建模的贝叶斯收缩框架

研究问题
摘要称,研究问题是如何在高维、含噪且由稀疏信号间复杂交互支配的生物数据中,实现可解释且可靠的特征选择与交互识别,例如基因组中基序交互的识别。
方法与思路
作者提出 BaGGLS,一个用于含特征交互的高维生物推断的概率二值回归模型;采用与交互项组结构对应的贝叶斯组全局-局部收缩先验以促进稀疏性,并用部分因子化变分近似实现可扩展推断。
材料陈述的贡献
摘要称,模拟结果显示 BaGGLS 在交互检测上优于其他方法,且比 horseshoe 先验下的 MCMC 抽样快许多倍;作者还在基序扫描输出与深度学习模型噪声归因分数的交互发现中展示了其可用性。
阅读关注点
阅读全文时应核对:先验的具体形式与组结构设定、变分近似的近似质量与理论保证、模拟设计及对比方法是否公平、加速倍数的计算口径,以及真实数据中交互结果的生物学验证方式。
阅读边界
仅凭摘要无法判断识别假设、理论性质、模拟与实证的具体数值结果及可复现性;该文为 arXiv 预印本,未经同行评审或期刊接收,结论应视为作者自述。

原文摘要

Biological data sets are often high-dimensional, noisy, and governed by complex interactions among sparse signals. This poses major challenges for interpretability and reliable feature selection. Tasks such as identifying motif interactions in genomics exemplify these difficulties, as only a small subset of biologically relevant features (e.g., motifs) are typically active, and their effects are often non-linear and context-dependent. While statistical approaches often result in more interpretable models, deep learning models have proven effective in modeling complex interactions and prediction accuracy, yet their black-box nature limits interpretability. We introduce BaGGLS, a flexible and interpretable probabilistic binary regression model designed for high-dimensional biological inference involving feature interactions. BaGGLS incorporates a Bayesian group global-local shrinkage prior, aligned with the group structure introduced by interaction terms. This prior encourages sparsity while retaining interpretability, helping to isolate meaningful signals and suppress noise. To enable scalable inference, we employ a partially factorized variational approximation that captures posterior skewness and supports efficient learning even in large feature spaces. In extensive simulations, we can show that BaGGLS outperforms the other methods with regard to interaction detection and is many times faster than MCMC sampling under the horseshoe prior. We also demonstrate the usefulness of BaGGLS in the context of interaction discovery from motif scanner outputs and noisy attribution scores from deep learning models. This shows that BaGGLS is a promising approach for uncovering biologically relevant interaction patterns, with potential applicability across a range of high-dimensional tasks in computational biology.

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