scholarly journals Post-inference Methods of Prior Knowledge Incorporation in Gene Regulatory Network Inference

2017 ◽  
Author(s):  
Ajay Nair ◽  
Madhu Chetty
Keyword(s):  
Gene Expression ◽  
Prior Knowledge ◽  
Gene Expression Data ◽  
Regulatory Network ◽  
Expression Data ◽  
Inference Method ◽  
Regulatory Interactions ◽  
A Cell ◽  
Gene Regulatory ◽  
Inference Methods

AbstractThe regulatory interactions in a cell control cellular response to environmental and genetic perturbations. Gene regulatory network (GRN) inference from high-throughput gene expression data helps to identify unknown regulatory interactions in a cell. One of the main challenges in the GRN inference is to identify complex biological interactions from the limited information contained in the gene expression data. Using prior biological knowledge, in addition to the gene expression data, is a common method to overcome this challenge. However, only a few GRN inference methods can inherently incorporate the prior knowledge and these methods are also not among the best-ranked in benchmarking studies.We propose to incorporate the prior knowledge after the GRN inference so that any inference method can be used. Two algorithms have been developed and tested on the well studied Escherichia coli, yeast, and realistic in silico networks. Their accuracy is higher than the best-ranking method in the latest community-wide benchmarking study. Further, one of the algorithms identifies and removes wrong interactions predicted by the inference methods. With half of the available prior knowledge of interactions, around 970 additional correct edges were obtained and 1300 wrong interactions were removed. Moreover, the limitation that only a few GRN inference methods can incorporate the prior knowledge is overcome. Therefore, a post-inference method of incorporating the prior knowledge improves accuracy, removes wrong edges, and overcomes the limitation of GRN inference methods.

scholarly journals Inference of Genetic Networks From Time-Series and Static Gene Expression Data: Combining a Random-Forest-Based Inference Method With Feature Selection Methods

2020 ◽  
Vol 11 ◽  
Author(s):  
Shuhei Kimura ◽  
Ryo Fukutomi ◽  
Masato Tokuhisa ◽  
Mariko Okada
Keyword(s):  
Gene Expression ◽  
Feature Selection ◽  
Random Forest ◽  
Gene Expression Data ◽  
Computational Cost ◽  
Expression Data ◽  
Selection Methods ◽  
Inference Method ◽  
Combined Application ◽  
Inference Methods

Several researchers have focused on random-forest-based inference methods because of their excellent performance. Some of these inference methods also have a useful ability to analyze both time-series and static gene expression data. However, they are only of use in ranking all of the candidate regulations by assigning them confidence values. None have been capable of detecting the regulations that actually affect a gene of interest. In this study, we propose a method to remove unpromising candidate regulations by combining the random-forest-based inference method with a series of feature selection methods. In addition to detecting unpromising regulations, our proposed method uses outputs from the feature selection methods to adjust the confidence values of all of the candidate regulations that have been computed by the random-forest-based inference method. Numerical experiments showed that the combined application with the feature selection methods improved the performance of the random-forest-based inference method on 99 of the 100 trials performed on the artificial problems. However, the improvement tends to be small, since our combined method succeeded in removing only 19% of the candidate regulations at most. The combined application with the feature selection methods moreover makes the computational cost higher. While a bigger improvement at a lower computational cost would be ideal, we see no impediments to our investigation, given that our aim is to extract as much useful information as possible from a limited amount of gene expression data.

PAGeneRN

2020 ◽  
pp. 1052-1075 ◽  
Author(s):  
Dina Elsayad ◽  
A. Ali ◽  
Howida A. Shedeed ◽  
Mohamed F. Tolba
Keyword(s):  
Gene Expression ◽  
Data Analysis ◽  
Network Analysis ◽  
Gene Regulatory Network ◽  
Gene Expression Data ◽  
Regulatory Network ◽  
Regulatory Networks ◽  
Expression Data ◽  
Gene Expression Data Analysis ◽  
Gene Regulatory

The gene expression analysis is an important research area of Bioinformatics. The gene expression data analysis aims to understand the genes interacting phenomena, gene functionality and the genes mutations effect. The Gene regulatory network analysis is one of the gene expression data analysis tasks. Gene regulatory network aims to study the genes interactions topological organization. The regulatory network is critical for understanding the pathological phenotypes and the normal cell physiology. There are many researches that focus on gene regulatory network analysis but unfortunately some algorithms are affected by data size. Where, the algorithm runtime is proportional to the data size, therefore, some parallel algorithms are presented to enhance the algorithms runtime and efficiency. This work presents a background, mathematical models and comparisons about gene regulatory networks analysis different techniques. In addition, this work proposes Parallel Architecture for Gene Regulatory Network (PAGeneRN).

scholarly journals Neural Gene Network Constructor: A Neural Based Model for Reconstructing Gene Regulatory Network

2019 ◽  
Author(s):  
Zhang Zhang ◽  
Lifei Wang ◽  
Shuo Wang ◽  
Ruyi Tao ◽  
Jingshu Xiao ◽  
...  
Keyword(s):  
Gene Expression ◽  
Gene Regulatory Network ◽  
Gene Expression Data ◽  
Gene Regulatory Networks ◽  
Network Structure ◽  
Regulatory Network ◽  
Gene Network ◽  
Regulatory Networks ◽  
Expression Data ◽  
Gene Regulatory

SummaryReconstructing gene regulatory networks (GRNs) and inferring the gene dynamics are important to understand the behavior and the fate of the normal and abnormal cells. Gene regulatory networks could be reconstructed by experimental methods or from gene expression data. Recent advances in Single Cell RNA sequencing technology and the computational method to reconstruct trajectory have generated huge scRNA-seq data tagged with additional time labels. Here, we present a deep learning model “Neural Gene Network Constructor” (NGNC), for inferring gene regulatory network and reconstructing the gene dynamics simultaneously from time series gene expression data. NGNC is a model-free heterogenous model, which can reconstruct any network structure and non-linear dynamics. It consists of two parts: a network generator which incorporating gumbel softmax technique to generate candidate network structure, and a dynamics learner which adopting multiple feedforward neural networks to predict the dynamics. We compare our model with other well-known frameworks on the data set generated by GeneNetWeaver, and achieve the state of the arts results both on network reconstruction and dynamics learning.

scholarly journals Approximated Gene Expression Trajectories (AGETs) for Gene Regulatory Network Inference on Cell Tracks

2022 ◽  
Author(s):  
Kay Spiess ◽  
Timothy Fulton ◽  
Seogwon Hwang ◽  
Kane Toh ◽  
Dillan Saunders ◽  
...  
Keyword(s):  
Gene Expression ◽  
Pattern Formation ◽  
Gene Regulatory Network ◽  
Gene Expression Data ◽  
Regulatory Network ◽  
Quantitative Data ◽  
Expression Data ◽  
Cell Movements ◽  
Reverse Engineer ◽  
Gene Regulatory

The study of pattern formation has benefited from reverse-engineering gene regulatory network (GRN) structure from spatio-temporal quantitative gene expression data. Traditional approaches omit tissue morphogenesis, hence focusing on systems where the timescales of pattern formation and morphogenesis can be separated. In such systems, pattern forms as an emergent property of the underlying GRN. This is not the case in many animal patterning systems, where patterning and morphogenesis are simultaneous. To address pattern formation in these systems we need to adapt our methodologies to explicitly accommodate cell movements and tissue shape changes. In this work we present a novel framework to reverse-engineer GRNs underlying pattern formation in tissues experiencing morphogenetic changes and cell rearrangements. By combination of quantitative data from live and fixed embryos we approximate gene expression trajectories (AGETs) in single cells and use a subset to reverse-engineer candidate GRNs using a Markov Chain Monte Carlo approach. GRN fit is assessed by simulating on cell tracks (live-modelling) and comparing the output to quantitative data-sets. This framework outputs candidate GRNs that recapitulate pattern formation at the level of the tissue and the single cell. To our knowledge, this inference methodology is the first to integrate cell movements and gene expression data, making it possible to reverse-engineer GRNs patterning tissues undergoing morphogenetic changes.

Identifying differential networks based on multi-platform gene expression data

2017 ◽  
Vol 13 (1) ◽  
pp. 183-192 ◽  
Author(s):  
Le Ou-Yang ◽  
Hong Yan ◽  
Xiao-Fei Zhang
Keyword(s):  
Gene Expression ◽  
Gene Regulatory Network ◽  
Gene Expression Data ◽  
Regulatory Network ◽  
Disease Development ◽  
Expression Data ◽  
Biological Mechanisms ◽  
Disease States ◽  
Gene Regulatory ◽  
Differential Networks

Exploring how the structure of a gene regulatory network differs between two different disease states is fundamental for understanding the biological mechanisms behind disease development and progression.

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