MODalyseR—a novel software for inference of disease module hub regulators identified a putative multiple sclerosis regulator supported by independent eQTL dataShow others and affiliations
2022 (English)In: Bioinformatics Advances, E-ISSN 2635-0041, Vol. 2, no 1, article id vbac006Article in journal (Refereed) Published
Abstract [en]
MotivationNetwork-based disease modules have proven to be a powerful concept for extracting knowledge about disease mechanisms, predicting for example disease risk factors and side effects of treatments. Plenty of tools exist for the purpose of module inference, but less effort has been put on simultaneously utilizing knowledge about regulatory mechanisms for predicting disease module hub regulators.
ResultsWe developed MODalyseR, a novel software for identifying disease module regulators and reducing modules to the most disease-associated genes. This pipeline integrates and extends previously published software packages MODifieR and ComHub and hereby provides a user-friendly network medicine framework combining the concepts of disease modules and hub regulators for precise disease gene identification from transcriptomics data. To demonstrate the usability of the tool, we designed a case study for multiple sclerosis that revealed IKZF1 as a promising hub regulator, which was supported by independent ChIP-seq data.
Availability and implementationMODalyseR is available as a Docker image at https://hub.docker.com/r/ddeweerd/modalyser with user guide and installation instructions found at https://gustafsson-lab.gitlab.io/MODalyseR/.
Supplementary informationSupplementary data are available at Bioinformatics Advances online.
Place, publisher, year, edition, pages
Oxford University Press, 2022. Vol. 2, no 1, article id vbac006
National Category
Bioinformatics and Systems Biology
Research subject
Bioinformatics
Identifiers
URN: urn:nbn:se:his:diva-21058DOI: 10.1093/bioadv/vbac006ISI: 001153137500002PubMedID: 36699378Scopus ID: 2-s2.0-85148565848OAI: oai:DiVA.org:his-21058DiVA, id: diva2:1651870
Funder
Knowledge Foundation, dnr HSK219/26Swedish Foundation for Strategic Research, SB16-0011Swedish Research Council, 2019-04193
Note
CC BY 4.0
Correspondence: Mika Gustafsson
Advance Access Publication Date: 25 January 2022
Funding: This work was supported by the Knowledge Foundation [dnr HSK219/26]; Swedish Foundation for Strategic Research [SB16-0011]; and Swedish Research Council [grant 2019-04193].
2022-04-132022-04-132024-05-20Bibliographically approved