CoVar: A generalizable machine learning approach to identify the coordinated regulators driving variational gene expression
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Abstract
Network inference is used to model transcriptional, signaling, and metabolic interactions among genes, proteins, and metabolites that identify biological pathways influencing disease pathogenesis. Advances in machine learning (ML)-based inference models exhibit the predictive capabilities of capturing latent patterns in genomic data. Such models are emerging as an alternative to the statistical models identifying causative factors driving complex diseases. We present CoVar, an inference framework that builds upon the properties of existing inference models, to find the central genes driving perturbed gene expression across biological states. We leverage ML-based network inference to find networks that capture the strength of regulatory interactions. Our model first pinpoints a subset of genes, termed variational, whose expression variabilities typify the differences in network connectivity between the control and perturbed data. Variational genes, by being differentially expressed themselves or possessing differentially expressed neighbor genes, capture gene expression variability. CoVar then creates subnetworks comprising variational genes and their strongly connected neighbor genes and identifies core genes central to these subnetworks that influence the bulk of the variational activity. Through the analysis of yeast expression data perturbed by the deletion of the mitochondrial genome, we show that CoVar identifies key genes not found through independent differential expression analysis.
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- Network analysis of differential expression for the identification of disease-causing genes. via crossref
- doi:10.1161/circgenetics.113.000123 via crossref
- doi:10.1007/978-3-319-78512-7 via crossref
- doi:10.1016/j.jtbi.2007.05.038 via crossref
- doi:10.1371/journal.pcbi.0030207 via crossref
- doi:10.1186/1471-2105-9-1 via crossref
- doi:10.1093/bib/bbw139 via crossref
- doi:10.3389/fgene.2021.726596 via crossref
- doi:10.1093/bioinformatics/btl391 via crossref
- doi:10.1093/bioinformatics/18.suppl_2.s231 via crossref
- doi:10.1371/journal.pone.0006799 via crossref
- doi:10.1534/g3.115.018127 via crossref
- doi:10.1093/bioinformatics/btz529 via crossref
- doi:10.1093/bioinformatics/btab502 via crossref
- doi:10.1007/978-3-319-78512-7 via crossref
- doi:10.1016/j.jtbi.2007.05.038 via crossref
- doi:10.3390/app11062857 via crossref
- doi:10.1371/journal.pone.0012776 via crossref
- doi:10.1186/gb-2002-3-2-reviews0003 via crossref
- doi:10.1093/bioinformatics/btm344 via crossref
- doi:10.1073/pnas.0601602103 via crossref
- doi:10.1103/physrevlett.100.118703 via crossref
- doi:10.1016/0012-365x(92)90282-k via crossref
- doi:10.1073/pnas.200327197 via crossref
- doi:10.1137/s003614450342480 via crossref
- doi:10.1186/1471-2105-7-1 via crossref
- doi:10.15252/embr.202051606 via crossref
- doi:10.1093/nar/gkw377 via crossref
- doi:10.1021/acs.accounts.5b00150 via crossref
- doi:10.1186/gb-2006-7-s1-s10 via crossref
- doi:10.1126/sciadv.abl8716 via crossref
- doi:10.1128/mcb.15.11.6232 via crossref
- doi:10.1093/jxb/erz525 via crossref
- doi:10.1091/mbc.e17-10-0619 via crossref
- doi:10.1074/jbc.m708232200 via crossref
- doi:10.1371/journal.pone.0134326 via crossref
- doi:10.1034/j.1600-0854.2001.002006368.x via crossref
- doi:10.1161/circresaha.113.300939 via crossref
- doi:10.1182/blood.v114.22.3642.3642 via crossref
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