Annotating publicly-available samples and studies using interpretable modeling of unstructured metadata.

IF 6.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Hao Yuan, Parker Hicks, Mansooreh Ahmadian, Kayla A Johnson, Lydia Valtadoros, Arjun Krishnan
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引用次数: 0

Abstract

Reusing massive collections of publicly available biomedical data can significantly impact knowledge discovery. However, these public samples and studies are typically described using unstructured plain text, hindering the findability and further reuse of the data. To combat this problem, we propose txt2onto 2.0, a general-purpose method based on natural language processing and machine learning for annotating biomedical unstructured metadata to controlled vocabularies of diseases and tissues. Compared to the previous version (txt2onto 1.0), which uses numerical embeddings as features, this new version uses words as features, resulting in improved interpretability and performance, especially when few positive training instances are available. Txt2onto 2.0 uses embeddings from a large language model during prediction to deal with unseen-yet-relevant words related to each disease and tissue term being predicted from the input text, thereby explaining the basis of every annotation. We demonstrate the generalizability of txt2onto 2.0 by accurately predicting disease annotations for studies from independent datasets, using proteomics and clinical trials as examples. Overall, our approach can annotate biomedical text regardless of experimental types or sources. Code, data, and trained models are available at https://github.com/krishnanlab/txt2onto2.0.

使用非结构化元数据的可解释建模对公开可用的样本和研究进行注释。
重用大量可公开获得的生物医学数据可以显著影响知识发现。然而,这些公共样本和研究通常使用非结构化纯文本进行描述,阻碍了数据的可查找性和进一步重用。为了解决这个问题,我们提出了txt2onto 2.0,这是一种基于自然语言处理和机器学习的通用方法,用于将生物医学非结构化元数据注释到疾病和组织的受控词汇表中。与使用数字嵌入作为特征的上一个版本(txt2onto 1.0)相比,这个新版本使用单词作为特征,从而提高了可解释性和性能,特别是在可用的正面训练实例很少的情况下。Txt2onto 2.0在预测期间使用来自大型语言模型的嵌入来处理从输入文本中预测的与每种疾病和组织术语相关的未见但相关的单词,从而解释每个注释的基础。我们以蛋白质组学和临床试验为例,通过准确预测来自独立数据集的研究的疾病注释,证明了txt22.0的通用性。总的来说,我们的方法可以注释生物医学文本,而不考虑实验类型或来源。代码、数据和经过训练的模型可在https://github.com/krishnanlab/txt2onto2.0上获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Briefings in bioinformatics
Briefings in bioinformatics 生物-生化研究方法
CiteScore
13.20
自引率
13.70%
发文量
549
审稿时长
6 months
期刊介绍: Briefings in Bioinformatics is an international journal serving as a platform for researchers and educators in the life sciences. It also appeals to mathematicians, statisticians, and computer scientists applying their expertise to biological challenges. The journal focuses on reviews tailored for users of databases and analytical tools in contemporary genetics, molecular and systems biology. It stands out by offering practical assistance and guidance to non-specialists in computerized methodologies. Covering a wide range from introductory concepts to specific protocols and analyses, the papers address bacterial, plant, fungal, animal, and human data. The journal's detailed subject areas include genetic studies of phenotypes and genotypes, mapping, DNA sequencing, expression profiling, gene expression studies, microarrays, alignment methods, protein profiles and HMMs, lipids, metabolic and signaling pathways, structure determination and function prediction, phylogenetic studies, and education and training.
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