Summary: In systems biology, it is challenging to accurately infer a regulatory network from time-series gene expression data, and a variety of methods have been proposed. Most of them were computationally inefficient in inferring very large networks, though, because of the increasing number of candidate regulatory genes. Although a recent approach called GABNI (genetic algorithm-based Boolean network inference) was presented to resolve this problem using a genetic algorithm, there is room for performance improvement because it employed a limited representation model of regulatory functions.In this regard, we devised a novel genetic algorithm combined with a neural network for the Boolean network inference, where a neural network is used to represent the regulatory function instead of an incomplete Boolean truth table used in the GABNI. In addition, our new method extended the range of the time-step lag parameter value between the regulatory and the target genes for more flexible representation of the regulatory function. Extensive simulations with the gene expression datasets of the artificial and real networks were conducted to compare our method with five well-known existing methods including GABNI. Our proposed method significantly outperformed them in terms of both structural and dynamics accuracy.
Conclusion: Our method can be a promising tool to infer a large-scale Boolean regulatory network from time-series gene expression data.
Availability And Implementation: The source code is freely available at https://github.com/kwon-uou/NNBNI.
Supplementary Information: Supplementary data are available at Bioinformatics online.
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Nat Commun
January 2025
Rudolf Peierls Centre for Theoretical Physics, University of Oxford, Oxford, UK.
The remarkable performance of overparameterized deep neural networks (DNNs) must arise from an interplay between network architecture, training algorithms, and structure in the data. To disentangle these three components for supervised learning, we apply a Bayesian picture based on the functions expressed by a DNN. The prior over functions is determined by the network architecture, which we vary by exploiting a transition between ordered and chaotic regimes.
View Article and Find Full Text PDFGenes (Basel)
November 2024
Faculty of Engineering, Multimedia University, Cyberjaya 63000, Selangor, Malaysia.
Background: In the realm of system biology, it is a challenging endeavor to infer a gene regulatory network from time-series gene expression data. Numerous Boolean network inference techniques have emerged for reconstructing a gene regulatory network from a time-series gene expression dataset. However, most of these techniques pose scalability concerns given their capability to consider only two to three regulatory genes over a specific target gene.
View Article and Find Full Text PDFEntropy (Basel)
December 2024
Department of Physics, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Can we turn AI black boxes into code? Although this mission sounds extremely challenging, we show that it is not entirely impossible by presenting a proof-of-concept method, MIPS, that can synthesize programs based on the automated mechanistic interpretability of neural networks trained to perform the desired task, auto-distilling the learned algorithm into Python code. We test MIPS on a benchmark of 62 algorithmic tasks that can be learned by an RNN and find it highly complementary to GPT-4: MIPS solves 32 of them, including 13 that are not solved by GPT-4 (which also solves 30). MIPS uses an integer autoencoder to convert the RNN into a finite state machine, then applies Boolean or integer symbolic regression to capture the learned algorithm.
View Article and Find Full Text PDFBMJ Open
January 2025
Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
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View Article and Find Full Text PDFFront Med (Lausanne)
December 2024
Social Determinants of Health Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Background: Alzheimer's disease (AD) is a chronic, progressive neurodegenerative disorder characterized by cognitive decline, memory loss, and impaired reasoning. It is the leading cause of dementia in older adults, marked by the pathological accumulation of amyloid-beta plaques and neurofibrillary tangles. These pathological changes lead to widespread neuronal damage, significantly impacting daily functioning and quality of life.
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