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Helena Ahlfors

dblp:176/7338 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2016
0000-0002-8183-0895ORCID · reported

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

Applied, interdisciplinary, general and emerging computing · 1

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
Computational science and engineering · 64% Bioinformatics and computational biology · 36%

Topics — the 5 heaviest of 5, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Computational science and engineering › dynamic network analysis
dynamic network inference
0.212016
Data-driven mechanistic analysis method to reveal dynamically evolving regulatory networks · Bioinform. 2016
Bioinformatics and computational biology › biological network › network biology › network inference
gene regulatory network inference
0.212016
Data-driven mechanistic analysis method to reveal dynamically evolving regulatory networks · Bioinform. 2016
Computational science and engineering › dynamical systems › network dynamics
network rewiring
0.212016
Data-driven mechanistic analysis method to reveal dynamically evolving regulatory networks · Bioinform. 2016
Computational science and engineering › differential equations
ordinary differential equations
0.112016
Data-driven mechanistic analysis method to reveal dynamically evolving regulatory networks · Bioinform. 2016
Bioinformatics and computational biology
systems biology
0.112016
Data-driven mechanistic analysis method to reveal dynamically evolving regulatory networks · Bioinform. 2016

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

time-course RNA sequencing · 0.2ordinary differential equations · 0.2latent process model · 0.2
YearPublicationVenuePosition
2016 Data-driven mechanistic analysis method to reveal dynamically evolving regulatory networks
abstract
MOTIVATION: Mechanistic models based on ordinary differential equations provide powerful and accurate means to describe the dynamics of molecular machinery which orchestrates gene regulation. When combined with appropriate statistical techniques, mechanistic models can be calibrated using experimental data and, in many cases, also the model structure can be inferred from time-course measurements. However, existing mechanistic models are limited in the sense that they rely on the assumption of static network structure and cannot be applied when transient phenomena affect, or rewire, the network structure. In the context of gene regulatory network inference, network rewiring results from the net impact of possible unobserved transient phenomena such as changes in signaling pathway activities or epigenome, which are generally difficult, but important, to account for. RESULTS: We introduce a novel method that can be used to infer dynamically evolving regulatory networks from time-course data. Our method is based on the notion that all mechanistic ordinary differential equation models can be coupled with a latent process that approximates the network structure rewiring process. We illustrate the performance of the method using simulated data and, further, we apply the method to study the regulatory interactions during T helper 17 (Th17) cell differentiation using time-course RNA sequencing data. The computational experiments with the real data show that our method is capable of capturing the experimentally verified rewiring effects of the core Th17 regulatory network. We predict Th17 lineage specific subnetworks that are activated sequentially and control the differentiation process in an overlapping manner. AVAILABILITY AND IMPLEMENTATION: An implementation of the method is available at http://research.ics.aalto.fi/csb/software/lem/ CONTACTS: [email protected] or [email protected].
Jukka Intosalmi, Kari Nousiainen, Helena Ahlfors, Harri Lähdesmäki
Bioinform.3