Olof Rundquist

dblp:310/7152 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2021
0000-0002-1424-3658ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene regulation › gene regulatory network
gene regulatory network analysis
0.512021
Using high-throughput multi-omics data to investigate structural balance in elementary gene regulatory network motifs · Bioinform. 2021
Bioinformatics and computational biology › sequence analysis › motif discovery
regulatory motif discovery
0.512021
Using high-throughput multi-omics data to investigate structural balance in elementary gene regulatory network motifs · Bioinform. 2021
Bioinformatics and computational biology
multi-omics data integration
0.112021
Using high-throughput multi-omics data to investigate structural balance in elementary gene regulatory network motifs · Bioinform. 2021

Methods — techniques the papers use, named apart from their topics

partial correlation · 0.5graphical model · 0.5conditional independence · 0.5
YearPublicationVenuePosition
2021 Using high-throughput multi-omics data to investigate structural balance in elementary gene regulatory network motifs
abstract
MOTIVATION: The simultaneous availability of ATAC-seq and RNA-seq experiments allows to obtain a more in-depth knowledge on the regulatory mechanisms occurring in gene regulatory networks. In this article, we highlight and analyze two novel aspects that leverage on the possibility of pairing RNA-seq and ATAC-seq data. Namely we investigate the causality of the relationships between transcription factors, chromatin and target genes and the internal consistency between the two omics, here measured in terms of structural balance in the sample correlations along elementary length-3 cycles. RESULTS: We propose a framework that uses the a priori knowledge on the data to infer elementary causal regulatory motifs (namely chains and forks) in the network. It is based on the notions of conditional independence and partial correlation, and can be applied to both longitudinal and non-longitudinal data. Our analysis highlights a strong connection between the causal regulatory motifs that are selected by the data and the structural balance of the underlying sample correlation graphs: strikingly, >97% of the selected regulatory motifs belong to a balanced subgraph. This result shows that internal consistency, as measured by structural balance, is close to a necessary condition for 3-node regulatory motifs to satisfy causality rules. AVAILABILITY AND IMPLEMENTATION: The analysis was carried out in MATLAB and the code can be found at https://github.com/albertozenere/Multi-omics-elementary-regulatory-motifs. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Alberto Zenere, Olof Rundquist, Mika Gustafsson, Claudio Altafini
Bioinform.2