scholarly journals Space-log: a novel approach to inferring gene-gene net-works using SPACE model with log penalty

F1000Research ◽  
2022 ◽  
Vol 9 ◽  
pp. 1159
Author(s):  
Qian (Vicky) Wu ◽  
Wei Sun ◽  
Li Hsu

Gene expression data have been used to infer gene-gene networks (GGN) where an edge between two genes implies the conditional dependence of these two genes given all the other genes. Such gene-gene networks are of-ten referred to as gene regulatory networks since it may reveal expression regulation. Most of existing methods for identifying GGN employ penalized regression with L1 (lasso), L2 (ridge), or elastic net penalty, which spans the range of L1 to L2 penalty. However, for high dimensional gene expression data, a penalty that spans the range of L0 and L1 penalty, such as the log penalty, is often needed for variable selection consistency. Thus, we develop a novel method that em-ploys log penalty within the framework of an earlier network identification method space (Sparse PArtial Correlation Estimation), and implement it into a R package space-log. We show that the space-log is computationally efficient (source code implemented in C), and has good performance comparing with other methods, particularly for networks with hubs.Space-log is open source and available at GitHub, https://github.com/wuqian77/SpaceLog

F1000Research ◽  
2020 ◽  
Vol 9 ◽  
pp. 1159
Author(s):  
Qian (Vicky) Wu ◽  
Wei Sun ◽  
Li Hsu

Gene expression data have been used to infer gene-gene networks (GGN) where an edge between two genes implies the conditional dependence of these two genes given all the other genes. Such gene-gene networks are of-ten referred to as gene regulatory networks since it may reveal expression regulation. Most of existing methods for identifying GGN employ penalized regression with L1 (lasso), L2 (ridge), or elastic net penalty, which spans the range of L1 to L2 penalty. However, for high dimensional gene expression data, a penalty that spans the range of L0 and L1 penalty, such as the log penalty, is often needed for variable selection consistency. Thus, we develop a novel method that em-ploys log penalty within the framework of an earlier network identification method space (Sparse PArtial Correlation Estimation), and implement it into a R package space-log. We show that the space-log is computationally efficient (source code implemented in C), and has good performance comparing with other methods, particularly for networks with hubs.Space-log is open source and available at GitHub, https://github.com/wuqian77/SpaceLog


2020 ◽  
Author(s):  
S. Thomas Kelly ◽  
Michael A. Black

SummaryTranscriptomic analysis is used to capture the molecular state of a cell or sample in many biological and medical applications. In addition to identifying alterations in activity at the level of individual genes, understanding changes in the gene networks that regulate fundamental biological mechanisms is also an important objective of molecular analysis. As a result, databases that describe biological pathways are increasingly uesad to assist with the interpretation of results from large-scale genomics studies. Incorporating information from biological pathways and gene regulatory networks into a genomic data analysis is a popular strategy, and there are many methods that provide this functionality for gene expression data. When developing or comparing such methods, it is important to gain an accurate assessment of their performance. Simulation-based validation studies are frequently used for this. This necessitates the use of simulated data that correctly accounts for pathway relationships and correlations. Here we present a versatile statistical framework to simulate correlated gene expression data from biological pathways, by sampling from a multivariate normal distribution derived from a graph structure. This procedure has been released as the graphsim R package on CRAN and GitHub (https://github.com/TomKellyGenetics/graphsim) and is compatible with any graph structure that can be described using the igraph package. This package allows the simulation of biological pathways from a graph structure based on a statistical model of gene expression.


2019 ◽  
Author(s):  
Xi Chen

AbstractBICORN is an R package developed to integrate prior transcription factor binding information and gene expression data for cis-regulatory module (CRM) inference. BICORN searches for a list of candidate CRMs from binary bindings on potential target genes. Applying Gibbs sampling, BICORN samples CRMs for each gene using the fitting performance of transcription factor activities and regulation strengths of TFs in each CRM on gene expression. Consequently, sparse regulatory networks are inferred as functional CRMs regulating target genes. The BICORN package is implemented in R and is available at https://cran.r-project.org/web/packages/BICORN/index.html.


2015 ◽  
Vol 11 (11) ◽  
pp. 3137-3148
Author(s):  
Nazanin Hosseinkhan ◽  
Peyman Zarrineh ◽  
Hassan Rokni-Zadeh ◽  
Mohammad Reza Ashouri ◽  
Ali Masoudi-Nejad

Gene co-expression analysis is one of the main aspects of systems biology that uses high-throughput gene expression data.


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