arXiv Open Access 2022

Biological Random Walks: multi-omics integration for disease gene prioritization

Michele Gentili Leonardo Martini Marialuisa Sponziello Luca Becchetti
Lihat Sumber

Abstrak

Motivation: Over the past decade, network-based approaches have proven useful in identifying disease modules within the human interactome, often providing insights into key mechanisms and guiding the quest for therapeutic targets. This is all the more important, since experimental investigation of potential gene candidates is an expensive task, thus not always a feasible option. On the other hand, many sources of biological information exist beyond the interactome and an important research direction is the design of effective techniques for their integration. Results: In this work, we introduce the Biological Random Walks (BRW) approach for disease gene prioritization in the human interactome. The proposed framework leverages multiple biological sources within an integrated framework. We perform an extensive, comparative study of BRW's performance against well-established baselines. Availability and implementation: All code is publicly available and can be downloaded at \url{https://github.com/LeoM93/BiologicalRandomWalks}. We used publicly available datasets, details on their retrieval and preprocessing are provided in the supplementary material.

Topik & Kata Kunci

Penulis (4)

M

Michele Gentili

L

Leonardo Martini

M

Marialuisa Sponziello

L

Luca Becchetti

Format Sitasi

Gentili, M., Martini, L., Sponziello, M., Becchetti, L. (2022). Biological Random Walks: multi-omics integration for disease gene prioritization. https://arxiv.org/abs/2211.13086

Akses Cepat

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Tahun Terbit
2022
Bahasa
en
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arXiv
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Open Access ✓