WeChat Mini Program
Old Version Features

PhysiBoSS 2.0: a Sustainable Integration of Stochastic Boolean and Agent-Based Modelling Frameworks

NPJ systems biology and applications(2023)SCI 2区SCI 1区

Life Science

Cited 3|Views23
Abstract
Cancer progression is a complex phenomenon that spans multiple scales from molecular to cellular and intercellular. Simulations can be used to perturb the underlying mechanisms of those systems and to generate hypotheses on novel therapies. We present a new version of PhysiBoSS, a multiscale modelling framework designed to cover multiple temporal and spatial scales, that improves its integration with PhysiCell, decoupling the cell agent simulations with the internal Boolean model in an easy-to-maintain computational framework. PhysiBoSS 2.0 is a redesign and reimplementation of PhysiBoSS, conceived as an add-on that expands the PhysiCell agent-based functionalities with intracellular cell signalling using MaBoSS having a decoupled, maintainable and model-agnostic design. PhysiBoSS 2.0 successfully reproduces simulations reported in the former version and expands its functionalities such as using user-defined models and cells’ specifications, having mechanistic submodels of substrate internalisation with ODEs and enabling the study of drug synergies. PhysiBoSS 2.0 is open-source and publicly available on GitHub () under the BSD 3-clause license with several repositories of accompanying interoperable tools. Additionally, a nanoHUB tool has been set up to ease the use of PhysiBoSS 2.0 (). ### Competing Interest Statement The authors have declared no competing interest.
More
Translated text
PDF
Bibtex
AI Read Science
AI Summary
AI Summary is the key point extracted automatically understanding the full text of the paper, including the background, methods, results, conclusions, icons and other key content, so that you can get the outline of the paper at a glance.
Example
Background
Key content
Introduction
Methods
Results
Related work
Fund
Key content
  • Pretraining has recently greatly promoted the development of natural language processing (NLP)
  • We show that M6 outperforms the baselines in multimodal downstream tasks, and the large M6 with 10 parameters can reach a better performance
  • We propose a method called M6 that is able to process information of multiple modalities and perform both single-modal and cross-modal understanding and generation
  • The model is scaled to large model with 10 billion parameters with sophisticated deployment, and the 10 -parameter M6-large is the largest pretrained model in Chinese
  • Experimental results show that our proposed M6 outperforms the baseline in a number of downstream tasks concerning both single modality and multiple modalities We will continue the pretraining of extremely large models by increasing data to explore the limit of its performance
Try using models to generate summary,it takes about 60s
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper
Data Disclaimer
The page data are from open Internet sources, cooperative publishers and automatic analysis results through AI technology. We do not make any commitments and guarantees for the validity, accuracy, correctness, reliability, completeness and timeliness of the page data. If you have any questions, please contact us by email: report@aminer.cn
Chat Paper

要点】:本文介绍了PhysiBoSS 2.0,一个整合了随机布尔模型和基于代理模型的跨尺度多物理生物建模框架,实现了与PhysiCell的更紧密集成,提高了模型的模块化和可维护性。

方法】:作者通过重新设计和实现PhysiBoSS,使其作为PhysiCell的扩展插件,利用MaBoSS进行细胞内信号传导的模拟,并确保了设计的解耦、可维护和模型无关性。

实验】:PhysiBoSS 2.0成功复现了前版本的模拟结果,并扩展了新功能,如支持用户定义模型和细胞规格、具有基于常微分方程(ODEs)的底物内化机制子模型,以及能够研究药物协同作用。该框架开源且可在GitHub上获取,同时配套了多个互操作工具仓库,并设置了nanoHUB工具以简化PhysiBoSS 2.0的使用。文中未具体提及使用的数据集名称。