ArticleFrontiers in bioinformatics2021
A Novel Calibration Step in Gene Co-Expression Network Construction.
Article in Frontiers in bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed, 1 citations in OpenAlex.
- Stage-Specific Reconstruction of Genome-Wide Genetic and Epigenetic Regulatory Networks Reveals Mechanistic Insights into Asthma Progression.International journal of molecular sciences · 2026Article
- SGCP: a spectral self-learning method for clustering genes in co-expression networks.BMC bioinformatics · 2024Article
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
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Abstract
High-throughput technologies such as DNA microarrays and RNA-sequencing are used to measure the expression levels of large numbers of genes simultaneously. To support the extraction of biological knowledge, individual gene expression levels are transformed to Gene Co-expression Networks (GCNs). In a GCN, nodes correspond to genes, and the weight of the connection between two nodes is a measure of similarity in the expression behavior of the two genes. In general, GCN construction and analysis includes three steps; 1) calculating a similarity value for each pair of genes 2) using these similarity values to construct a fully connected weighted network 3) finding clusters of genes in the network, commonly called modules. The specific implementation of these three steps can significantly impact the final output and the downstream biological analysis. GCN construction is a well-studied topic. Existing algorithms rely on relatively simple statistical and mathematical tools to implement these steps. Currently, software package WGCNA appears to be the most widely accepted standard. We hypothesize that the raw features provided by sequencing data can be leveraged to extract modules of higher quality. A novel preprocessing step of the gene expression data set is introduced that in effect calibrates the expression levels of individual genes, before computing pairwise similarities. Further, the similarity is computed as an inner-product of positive vectors. In experiments, this provides a significant improvement over WGCNA, as measured by aggregate
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