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AI 根据所提供的论文材料归类:摘要讨论生物数据的批次校正和潜在亚型聚类,未明确涉及结构变化、经济面板或其他所列计量细分问题。

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代码、数据与补充材料

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关注这篇论文的作者
Xiangyu Luo
Yingying Wei

未知亚型情况下的批次效应校正

研究问题
高通量数据同时存在技术批次效应与未知生物亚型时,如何区分二者、校正技术差异并保留具有解释意义的亚型特征?
方法与思路
作者将位置与尺度调整模型和基于模型的聚类结合为 BUS 模型,联合估计批次校正、样本亚型及区分亚型的特征。
材料陈述的贡献
摘要称,模型具有可识别性和线性阶计算复杂度,支持跨平台整合与批次间亚型数变化,并以模拟和乳腺癌数据评价。
阅读关注点
应核对可识别性证明与研究设计条件,尤其是批次和亚型混杂时的限制,以及亚型数选择、跨平台整合和复杂度计算口径。
阅读边界
仅据 OpenAlex 索引摘要,稿件版本未注明,不能推断刊本变化;具体识别条件未给出,生物学解释改善也缺少量化比较细节。

原文摘要

High-throughput experimental data are accumulating exponentially in public databases. Unfortunately, however, mining valid scientific discoveries from these abundant resources is hampered by technical artifacts and inherent biological heterogeneity. The former are usually termed “batch effects,” and the latter is often modeled by subtypes. Existing methods either tackle batch effects provided that subtypes are known or cluster subtypes assuming that batch effects are absent. Consequently, there is a lack of research on the correction of batch effects with the presence of unknown subtypes. Here, we combine a location-and-scale adjustment model and model-based clustering into a novel hybrid one, the batch-effects-correction-with-unknown-subtypes model (BUS). BUS is capable of (a) correcting batch effects explicitly, (b) grouping samples that share similar characteristics into subtypes, (c) identifying features that distinguish subtypes, (d) allowing the number of subtypes to vary from batch to batch, (e) integrating batches from different platforms, and (f) enjoying a linear-order computation complexity. We prove the identifiability of BUS and provide conditions for study designs under which batch effects can be corrected. BUS is evaluated by simulation studies and a real breast cancer dataset combined from three batches measured on two platforms. Results from the breast cancer dataset offer much better biological insights than existing methods. We implement BUS as a free Bioconductor package BUScorrect. Supplementary materials for this article are available online.

笔记与分组
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