ArticleBioinformatics (Oxford, England)2025
RVINN: a flexible modeling for inferring dynamic transcriptional and post-transcriptional regulation using physics-informed neural networks.
Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
summaryDynamic gene expression is controlled by transcriptional and post-transcriptional regulation. Recent studies on transcriptional bursting and buffering have increasingly highlighted the dynamic gene regulatory mechanisms. However, direct measurement techniques still face various constraints and require complementary methodologies, which are both comprehensive and versatile. To address this issue, inference approaches based on transcriptome data and differential equation models representing the messenger RNA lifecycle have been proposed. However, the inference of complex dynamics under diverse experimental conditions and biological scenarios remains challenging. In this study, we developed a flexible modeling using physics-informed neural networks and demonstrated its performance using simulation and experimental data. Our model has the ability to computationally revalidate and visualize dynamic biological phenomena, such as transcriptional ripple, co-bursting, and buffering in a breast cancer cell line. Furthermore, our results suggest putative molecular mechanisms underlying these phenomena. We propose a novel approach for inferring transcriptional and post-transcriptional regulation and expect to offer valuable insights for experimental and systems biology. AVAILABILITY AND IMPLEMENTATION: https://github.com/omuto/RVINN.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.