合并逻辑模型:急性髓性白血病建模中的应用。

Luna Xingyu Li, Boris Aguilar, John H Gennari, Guangrong Qin
{"title":"合并逻辑模型:急性髓性白血病建模中的应用。","authors":"Luna Xingyu Li, Boris Aguilar, John H Gennari, Guangrong Qin","doi":"10.1101/2024.09.13.612961","DOIUrl":null,"url":null,"abstract":"<p><strong>Motivation: </strong>Gene regulatory network (GRN) models provide mechanistic understanding of genetic interactions that regulate gene expression and, consequently, influence cellular behavior. Dysregulated gene expression plays a critical role in disease progression and treatment response, making GRN models a promising tool for precision medicine. While researchers have built many models to describe specific subsets of gene interactions, more comprehensive models that cover a broader range of genes are challenging to build. This necessitates the development of automated approaches for merging existing models.</p><p><strong>Results: </strong>We present LM-Merger, a workflow for semi-automatically merging logical GRN models. The workflow consists of five main steps: (a) model identification, (b) model standardization and annotation, (c) model verification, (d) model merging, and (d) model evaluation. We demonstrate the feasibility and benefit of this workflow with two pairs of published models pertaining to acute myeloid leukemia (AML). The integrated models were able to retain the predictive accuracy of the original models, while expanding coverage of the biological system. Notably, when applied to a new dataset, the integrated models outperformed the individual models in predicting patient response. This study highlights the potential of logical model merging to advance systems biology research and our understanding of complex diseases.</p><p><strong>Availability and implementation: </strong>The workflow and accompanying tools, including modules for model standardization, automated logical model merging, and evaluation, are available at https://github.com/IlyaLab/LogicModelMerger/.</p>","PeriodicalId":519960,"journal":{"name":"bioRxiv : the preprint server for biology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11429764/pdf/","citationCount":"0","resultStr":"{\"title\":\"LM-Merger: A workflow for merging logical models with an application to gene regulation.\",\"authors\":\"Luna Xingyu Li, Boris Aguilar, John H Gennari, Guangrong Qin\",\"doi\":\"10.1101/2024.09.13.612961\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Motivation: </strong>Gene regulatory network (GRN) models provide mechanistic understanding of genetic interactions that regulate gene expression and, consequently, influence cellular behavior. Dysregulated gene expression plays a critical role in disease progression and treatment response, making GRN models a promising tool for precision medicine. While researchers have built many models to describe specific subsets of gene interactions, more comprehensive models that cover a broader range of genes are challenging to build. This necessitates the development of automated approaches for merging existing models.</p><p><strong>Results: </strong>We present LM-Merger, a workflow for semi-automatically merging logical GRN models. The workflow consists of five main steps: (a) model identification, (b) model standardization and annotation, (c) model verification, (d) model merging, and (d) model evaluation. We demonstrate the feasibility and benefit of this workflow with two pairs of published models pertaining to acute myeloid leukemia (AML). The integrated models were able to retain the predictive accuracy of the original models, while expanding coverage of the biological system. Notably, when applied to a new dataset, the integrated models outperformed the individual models in predicting patient response. This study highlights the potential of logical model merging to advance systems biology research and our understanding of complex diseases.</p><p><strong>Availability and implementation: </strong>The workflow and accompanying tools, including modules for model standardization, automated logical model merging, and evaluation, are available at https://github.com/IlyaLab/LogicModelMerger/.</p>\",\"PeriodicalId\":519960,\"journal\":{\"name\":\"bioRxiv : the preprint server for biology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-12-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11429764/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"bioRxiv : the preprint server for biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1101/2024.09.13.612961\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv : the preprint server for biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.09.13.612961","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

基因调控网络(GRN)模型提供了对控制细胞行为各个方面的基因调控和相互作用的机理认识。虽然研究人员已经构建了基因调控网络模型来模拟特定的基因调控或相互作用,但很少有人将这些模型整合或合并成更大更全面的模型,以涵盖更多的基因,并提高预测生物过程的准确性。在这里,我们介绍了一种合并逻辑 GRN 模型的工作流程,该流程需要包括模型标准化、复制、合并和评估等连续步骤,并展示了该流程在急性髓性白血病(AML)研究中的应用。我们通过整合两对已发表的模型,证明了模型合并的可行性和优点。我们整合后的模型能够保持与原始出版物相似的准确性,同时增加了生物系统的覆盖面和可解释性。作者总结:在我们的研究中,我们解决了整合基因调控网络(GRN)模型以增强我们对复杂生物系统的理解所面临的挑战。基因调控网络是了解基因如何调控各种细胞行为的重要工具,但单个模型通常只关注特定的基因集或相互作用。我们提出了一种新颖的工作流程,将这些单个逻辑 GRN 模型合并成更全面的模型,为基因调控提供更广阔的视角。我们将这一工作流程应用于急性髓性白血病(AML),这是一种侵袭性很强的血癌。急性髓性白血病由于其遗传复杂性和经常出现的抗药性突变,治疗难度很大。我们的集成模型既保留了原始模型的准确性,又改进了生物过程的覆盖范围。这种方法通过组合描述急性髓细胞性白血病不同方面的模型,为了解该疾病的潜在机制提供了宝贵的见解。我们设想所提出的工作流程将改进预测,产生更深入的见解,并提高我们对急性髓细胞白血病等复杂疾病的理解和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
LM-Merger: A workflow for merging logical models with an application to gene regulation.

Motivation: Gene regulatory network (GRN) models provide mechanistic understanding of genetic interactions that regulate gene expression and, consequently, influence cellular behavior. Dysregulated gene expression plays a critical role in disease progression and treatment response, making GRN models a promising tool for precision medicine. While researchers have built many models to describe specific subsets of gene interactions, more comprehensive models that cover a broader range of genes are challenging to build. This necessitates the development of automated approaches for merging existing models.

Results: We present LM-Merger, a workflow for semi-automatically merging logical GRN models. The workflow consists of five main steps: (a) model identification, (b) model standardization and annotation, (c) model verification, (d) model merging, and (d) model evaluation. We demonstrate the feasibility and benefit of this workflow with two pairs of published models pertaining to acute myeloid leukemia (AML). The integrated models were able to retain the predictive accuracy of the original models, while expanding coverage of the biological system. Notably, when applied to a new dataset, the integrated models outperformed the individual models in predicting patient response. This study highlights the potential of logical model merging to advance systems biology research and our understanding of complex diseases.

Availability and implementation: The workflow and accompanying tools, including modules for model standardization, automated logical model merging, and evaluation, are available at https://github.com/IlyaLab/LogicModelMerger/.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信