GenomicLayers: sequence-based simulation of epi-genomes

Abstract Background Cellular development and differentiation in Eukaryotes depends upon sequential gene regulatory decisions that allow a single genome to encode many hundreds of distinct cellular phenotypes. Decisions are stored in the regulatory state of each cell, an important part of which is th...

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Main Author: Dave T. Gerrard
Format: Article
Language:English
Published: BMC 2025-08-01
Series:BMC Bioinformatics
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Online Access:https://doi.org/10.1186/s12859-025-06224-y
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author Dave T. Gerrard
author_facet Dave T. Gerrard
author_sort Dave T. Gerrard
collection DOAJ
description Abstract Background Cellular development and differentiation in Eukaryotes depends upon sequential gene regulatory decisions that allow a single genome to encode many hundreds of distinct cellular phenotypes. Decisions are stored in the regulatory state of each cell, an important part of which is the epi-genome—the collection of proteins, RNA and their specific associations with the genome. Additionally, further cellular responses are, in part, determined by this regulatory state. To date, models of regulatory state have failed to include the contingency of incoming regulatory signals on the current epi-genetic state and none have done so at the whole-genome level. Results Here we introduce GenomicLayers, a new R package to run rules-based simulations of epigenetic state changes genome-wide in Eukaryotes. Simulations model the accumulation of changes to genome-wide layers by user-specified binding factors. As a first exemplar, we show two versions of a simple model of the recruitment and spreading of epigenetic marks near telomeres in the yeast Saccharomyces cerevisiae. By combining the output from 100 runs of the simulation, we generate whole genome predictions of epigenetic state at 1 bp resolution. The example yeast models are included within a ‘vignette’ with the GenomicLayers package, which is available at https://github.com/davetgerrard/GenomicLayers . To demonstrate the use of GenomicLayers on the full human reference genome (hg38), we show the results from parameter refinement on a simplistic model of the action of pluripotency factors against a self-spreading repressor seeded at CpG islands. The human genome model is included in supplementary information as an R script. Conclusions GenomicLayers enables scientists working on diverse eukaryotic organisms to test models of gene regulation in silico. Applications include epigenetic silencing, activation by combinatorial binding of transcription factors and the sink effects caused by down-regulation of components of epigenetic regulators. The software is intended to be used to parameterise, refine and combine models and thereby capitalise on data from the thousands of studies of Eukaryotic epigenomes.
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spelling doaj-art-2b18cbb8b1304c74add93431a36ed7d22025-08-20T03:43:31ZengBMCBMC Bioinformatics1471-21052025-08-0126111010.1186/s12859-025-06224-yGenomicLayers: sequence-based simulation of epi-genomesDave T. Gerrard0Division of Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine & Health, The University of ManchesterAbstract Background Cellular development and differentiation in Eukaryotes depends upon sequential gene regulatory decisions that allow a single genome to encode many hundreds of distinct cellular phenotypes. Decisions are stored in the regulatory state of each cell, an important part of which is the epi-genome—the collection of proteins, RNA and their specific associations with the genome. Additionally, further cellular responses are, in part, determined by this regulatory state. To date, models of regulatory state have failed to include the contingency of incoming regulatory signals on the current epi-genetic state and none have done so at the whole-genome level. Results Here we introduce GenomicLayers, a new R package to run rules-based simulations of epigenetic state changes genome-wide in Eukaryotes. Simulations model the accumulation of changes to genome-wide layers by user-specified binding factors. As a first exemplar, we show two versions of a simple model of the recruitment and spreading of epigenetic marks near telomeres in the yeast Saccharomyces cerevisiae. By combining the output from 100 runs of the simulation, we generate whole genome predictions of epigenetic state at 1 bp resolution. The example yeast models are included within a ‘vignette’ with the GenomicLayers package, which is available at https://github.com/davetgerrard/GenomicLayers . To demonstrate the use of GenomicLayers on the full human reference genome (hg38), we show the results from parameter refinement on a simplistic model of the action of pluripotency factors against a self-spreading repressor seeded at CpG islands. The human genome model is included in supplementary information as an R script. Conclusions GenomicLayers enables scientists working on diverse eukaryotic organisms to test models of gene regulation in silico. Applications include epigenetic silencing, activation by combinatorial binding of transcription factors and the sink effects caused by down-regulation of components of epigenetic regulators. The software is intended to be used to parameterise, refine and combine models and thereby capitalise on data from the thousands of studies of Eukaryotic epigenomes.https://doi.org/10.1186/s12859-025-06224-yEpigenomeSimulationRGenomeDevelopment
spellingShingle Dave T. Gerrard
GenomicLayers: sequence-based simulation of epi-genomes
BMC Bioinformatics
Epigenome
Simulation
R
Genome
Development
title GenomicLayers: sequence-based simulation of epi-genomes
title_full GenomicLayers: sequence-based simulation of epi-genomes
title_fullStr GenomicLayers: sequence-based simulation of epi-genomes
title_full_unstemmed GenomicLayers: sequence-based simulation of epi-genomes
title_short GenomicLayers: sequence-based simulation of epi-genomes
title_sort genomiclayers sequence based simulation of epi genomes
topic Epigenome
Simulation
R
Genome
Development
url https://doi.org/10.1186/s12859-025-06224-y
work_keys_str_mv AT davetgerrard genomiclayerssequencebasedsimulationofepigenomes