Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Topology-based metrics for finding the optimal sparsity in gene regulatory network inference
Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics.
Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics. Stockholm University, Science for Life Laboratory (SciLifeLab).
Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics. Stockholm University, Science for Life Laboratory (SciLifeLab).ORCID iD: 0000-0002-6362-0659
Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics. Stockholm University, Science for Life Laboratory (SciLifeLab).ORCID iD: 0000-0002-9015-5588
Number of Authors: 42025 (English)In: Bioinformatics, ISSN 1367-4803, E-ISSN 1367-4811, Vol. 41, no 5, article id btaf120Article in journal (Refereed) Published
Abstract [en]

Motivation: Gene regulatory network (GRN) inference is a complex task aiming to unravel regulatory interactions between genes in a cell. A major shortcoming of most GRN inference methods is that they do not attempt to find the optimal sparsity, i.e. the single best GRN, which is important when applying GRN inference in a real situation. Instead, the sparsity tends to be controlled by an arbitrarily set hyperparameter. Results: In this paper, two new methods for predicting the optimal sparsity of GRNs are formulated and benchmarked on simulated perturbation-based gene expression data using four GRN inference methods: LASSO, Zscore, LSCON, and GENIE3. Both sparsity prediction methods are defined using the hypothesis that the topology of real GRNs is scale-free, and are evaluated based on their ability to predict the sparsity of the true GRN. The results show that the new topology-based approaches reliably predict a sparsity close to the true one. This ability is valuable for real-world applications where a single GRN is inferred from real data. In such situations, it is vital to be able to infer a GRN with the correct sparsity.

Place, publisher, year, edition, pages
2025. Vol. 41, no 5, article id btaf120
National Category
Biochemistry
Identifiers
URN: urn:nbn:se:su:diva-243341DOI: 10.1093/bioinformatics/btaf120ISI: 001483462800001Scopus ID: 2-s2.0-105004690157OAI: oai:DiVA.org:su-243341DiVA, id: diva2:1960093
Available from: 2025-05-22 Created: 2025-05-22 Last updated: 2025-05-22Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textScopus

Authority records

Garbulowski, MateuszHillerton, ThomasSonnhammer, Erik L. L.

Search in DiVA

By author/editor
Garbulowski, MateuszHillerton, ThomasSonnhammer, Erik L. L.
By organisation
Department of Biochemistry and BiophysicsScience for Life Laboratory (SciLifeLab)
In the same journal
Bioinformatics
Biochemistry

Search outside of DiVA

GoogleGoogle Scholar

doi
urn-nbn

Altmetric score

doi
urn-nbn
Total: 22 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf