TY - JOUR
T1 - Angiogenesis goes computational – The future way forward to discover new angiogenic targets?
AU - Subramanian, Abhishek
AU - Zakeri, Pooya
AU - Mousa, Mira
AU - Alnaqbi, Halima
AU - Alshamsi, Fatima Yousif
AU - Bettoni, Leo
AU - Damiani, Ernesto
AU - Alsafar, Habiba
AU - Saeys, Yvan
AU - Carmeliet, Peter
N1 - Funding Information:
The figures in the graphical abstract and Fig. 2 were created using BioRender.com. P.C. is supported by Grants from Methusalem funding (Flemish government), the Fund for Scientific Research-Flanders (FWO-Vlaanderen), the European Research Council (ERC) Advanced Research Grant EU-ERC74307 and the NNF Laureate Research Grant from Novo Nordisk Foundation (Denmark). This work was funded in part by Khalifa University as part of the Khalifa University and VIB-KU Leuven Biomedical Science Discovery Program.
Publisher Copyright:
© 2022 The Author(s)
PY - 2022/1
Y1 - 2022/1
N2 - Multi-omics technologies are being increasingly utilized in angiogenesis research. Yet, computational methods have not been widely used for angiogenic target discovery and prioritization in this field, partly because (wet-lab) vascular biologists are insufficiently familiar with computational biology tools and the opportunities they may offer. With this review, written for vascular biologists who lack expertise in computational methods, we aspire to break boundaries between both fields and to illustrate the potential of these tools for future angiogenic target discovery. We provide a comprehensive survey of currently available computational approaches that may be useful in prioritizing candidate genes, predicting associated mechanisms, and identifying their specificity to endothelial cell subtypes. We specifically highlight tools that use flexible, machine learning frameworks for large-scale data integration and gene prioritization. For each purpose-oriented category of tools, we describe underlying conceptual principles, highlight interesting applications and discuss limitations. Finally, we will discuss challenges and recommend some guidelines which can help to optimize the process of accurate target discovery.
AB - Multi-omics technologies are being increasingly utilized in angiogenesis research. Yet, computational methods have not been widely used for angiogenic target discovery and prioritization in this field, partly because (wet-lab) vascular biologists are insufficiently familiar with computational biology tools and the opportunities they may offer. With this review, written for vascular biologists who lack expertise in computational methods, we aspire to break boundaries between both fields and to illustrate the potential of these tools for future angiogenic target discovery. We provide a comprehensive survey of currently available computational approaches that may be useful in prioritizing candidate genes, predicting associated mechanisms, and identifying their specificity to endothelial cell subtypes. We specifically highlight tools that use flexible, machine learning frameworks for large-scale data integration and gene prioritization. For each purpose-oriented category of tools, we describe underlying conceptual principles, highlight interesting applications and discuss limitations. Finally, we will discuss challenges and recommend some guidelines which can help to optimize the process of accurate target discovery.
KW - Angiogenesis
KW - Biological networks
KW - Functional enrichment
KW - Gene prioritization
KW - Single-cell multi-omics
KW - Unsupervised and supervised data fusion
UR - http://www.scopus.com/inward/record.url?scp=85138451292&partnerID=8YFLogxK
U2 - 10.1016/j.csbj.2022.09.019
DO - 10.1016/j.csbj.2022.09.019
M3 - Review article
AN - SCOPUS:85138451292
SN - 2001-0370
VL - 20
SP - 5235
EP - 5255
JO - Computational and Structural Biotechnology Journal
JF - Computational and Structural Biotechnology Journal
ER -