Detection of markers for discrete phenotypes

Hannes Klarner, Elisa Tonello, L. Fontanals, F. Janody, C. Chaouiya, H. Siebert
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Abstract

Motivation: Capturing the molecular diversity of living cells is not straightforward. One approach is to measure molecular markers that serve as indicators of specific biological conditions or phenotypes. This is particularly relevant in modern medicine to provide precise diagnostics and pinpoint the best treatment for each patient. The challenge is to select a minimal set of markers whose activity patterns are in correspondence with the phenotypes of interest. Results: This article approaches the marker detection problem in the context of discrete phenotypes which arise, for example, from Boolean models of cellular networks. Mathematically this poses a combinatorial optimization problem with many answers. We propose a solution to this optimization problem that is based on the modelling language answer set programming (ASP). A case study of a death cell receptor network illustrates the methodology. Discussion and code: For code, discussions and reporting errors visit https://github.com/hklarner/detection_of_markers_for_discrete_phenotypes.
检测离散表型的标记
动机:捕捉活细胞的分子多样性并不简单。一种方法是测量作为特定生物条件或表型指标的分子标记。这在现代医学中尤其重要,以便为每位患者提供精确的诊断和确定最佳治疗方案。挑战在于选择最小的标记,其活动模式与感兴趣的表型相对应。结果:本文探讨了在出现的离散表型背景下的标记检测问题,例如,从细胞网络的布尔模型。从数学上讲,这是一个有许多答案的组合优化问题。本文提出了一种基于建模语言答案集编程(ASP)的优化方法。一个死亡细胞受体网络的案例研究说明了这种方法。讨论和代码:关于代码、讨论和错误报告,请访问https://github.com/hklarner/detection_of_markers_for_discrete_phenotypes。
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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