Multipath2.0: Extending Multilayer Reproducible Pathway Models with Omics Data

Zaynab Hammoud , Mohammad Al Maaz , Alicia D'Angelo , Frank Kramer
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引用次数: 0

Abstract

Background

Biological systems are often perceived as independent and consequently analyzed individually. In the field of omics, multiple disciplines target the study of specific types of molecules, such as genomics. The support of more data sources in these analyses is becoming more crucial for understanding the interplay of biological systems. However, this requires integration of heterogeneous knowledge, which is considered highly challenging in bioinformatics and biomedicine. Therefore, the R package Multipath was developed to model biological pathways as multilayered graphs and integrate influencing knowledge including proteins and drugs. In its previous form, Multipath generated multilayer models of BioPAX-encoded pathways and included features to integrate drug and protein information from DrugBank and UniProtKB respectively. Although the model showed remarkable utility, including further data sources ensures enriching and expanding its capabilities.

Results

In this paper, a new version Multipath 2.0 is presented. The update additionally supports the two databases KEGG Genes and OMIM, which serve as the source for gene and disease entries and interactions. Information on the interactions between the previously and newly added nodes are extracted and integrated. The Multipath 2.0 offers features to update the original multilayer model and integrate the corresponding nodes and edges into two additional layers referring to KEGG Genes and OMIM. Furthermore, the embedded nodes are inter- and intra-connected using interactions from the original and newly supported data sources.

Conclusion

The R Package Multipath is presented with the main functions that are newly developed to support the integration of the databases KEGG Genes and OMIM. The model comprises multiple information relevant to the analysis of pathway data, and offers a reproducible and simplified view of complex, intertwined systems. Through the application of such highly integrated models the inference of new knowledge becomes easier and contributes to many fields such as drug repurposing and biomarker discovery.
Multipath2.0:用组学数据扩展多层可复制通路模型
生物系统通常被认为是独立的,因此被单独分析。在组学领域,多个学科针对特定类型的分子进行研究,例如基因组学。在这些分析中,更多数据源的支持对于理解生物系统的相互作用变得越来越重要。然而,这需要整合异质知识,这在生物信息学和生物医学中被认为是极具挑战性的。因此,开发了R包Multipath,将生物通路建模为多层图,并整合包括蛋白质和药物在内的影响知识。在之前的形式中,Multipath生成了biopax编码通路的多层模型,并包含了分别从DrugBank和UniProtKB中整合药物和蛋白质信息的特征。尽管该模型显示了显著的实用性,但包括进一步的数据源确保了其功能的丰富和扩展。结果本文提出了一个新版本的Multipath 2.0。此次更新还支持两个数据库KEGG Genes和OMIM,这两个数据库是基因和疾病条目和相互作用的来源。提取和集成先前和新添加节点之间的交互信息。Multipath 2.0提供了更新原始多层模型的功能,并将相应的节点和边缘集成到两个额外的层中,参考KEGG Genes和OMIM。此外,使用来自原始和新支持的数据源的交互,嵌入节点可以相互连接和内部连接。结论为支持KEGG基因和OMIM数据库的集成,R包Multipath具有新开发的主要功能。该模型包含与路径数据分析相关的多个信息,并提供了复杂、相互交织的系统的可重复和简化视图。通过这种高度集成的模型的应用,新知识的推断变得更加容易,并有助于许多领域,如药物再利用和生物标志物的发现。
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
CiteScore
5.90
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0.00%
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