Evidence map›Paper›PMID 42282607›Full record

ArticlebioRxiv : the preprint server for biology2026

Epigenetic conditioning improves sequence-based modeling of gene regulation across cell types and alleles.

Oberon Dixon-Luinenburg, Ayesha Bajwa, Mitchell R Vollger, Andrew B Stergachis, Aaron Streets, Nilah M Ioannidis

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Oberon Dixon-LuinenburgUC Berkeley-UCSF Graduate Program in Bioengineering, University of California, Berkeley, Berkeley, CA, USA.ORCID 0000-0001-7251-309X
Ayesha BajwaCenter for Computational Biology, University of California, Berkeley, Berkeley, CA, USA.
Mitchell R VollgerDepartment of Human Genetics and Utah Center for Genetic Discovery, University of Utah, Salt Lake City, UT, USA.ORCID 0000-0002-8651-1615
Andrew B StergachisDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, USA.ORCID 0000-0002-1299-3674
Aaron StreetsCenter for Computational Biology, University of California, Berkeley, Berkeley, CA, USA.ORCID 0000-0002-3909-8389
Nilah M IoannidisCenter for Computational Biology, University of California, Berkeley, Berkeley, CA, USA.

Funding

Medical Genetics Training GrantT32GM007454 · NIGMS · UNIVERSITY OF WASHINGTON · PI Gail Pairitz Jarvik, Andrew Ben Stergachis · 1985 to 2026
$6.9M
Investigating the contribution of non-coding genetic variation to rare disordersDP5OD029630 · OD · UNIVERSITY OF WASHINGTON · PI STERGACHIS, ANDREW BEN · 2020 to 2024
$1.9M
Methods for Mapping Genetic Regulatory Elements in Single Cells and Single MoleculesR01HG012383 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI STREETS, AARON · 2022 to 2025
$1.8M
Tooling for accurately studying the epigenome along the human pangenome referenceU01HG013744 · NHGRI · UNIVERSITY OF WASHINGTON · PI STERGACHIS, ANDREW BEN · 2024 to 2024
$1.4M
The regulatory landscape of segmentally duplicated genes: Implications for human evolution and diseaseR00GM155552 · NIGMS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Mitchell R. Vollger · 2026 to 2026
$249k
The regulatory landscape of segmentally duplicated genes: Implications for human evolution and diseaseK99GM155552 · NIGMS · UNIVERSITY OF WASHINGTON · PI VOLLGER, MITCHELL R. · 2024 to 2025
$160k
NHGRI NIH HHS R01 HG012383NHGRI NIH HHS U01 HG013744NIGMS NIH HHS K99 GM155552NIGMS NIH HHS R00 GM155552NIGMS NIH HHS T32 GM007454NIH HHS DP5 OD029630
6 · The paper itself

Abstract

Epigenetic state modulates gene regulation in a manner not always predictable from DNA sequence alone, yet current genomic deep learning models do not leverage epigenetic state as input. We present MethylSeqNet, a model that conditions pretrained sequence embeddings on CpG methylation, a stable epigenetic mark increasingly available from long-read sequencing data. Using a novel conditioning mechanism enabling scalability and interpretability, MethylSeqNet improves predictions in cases where differential epigenetic state drives regulatory variation. We show improvements over a sequence-only baseline for cell-type-specific chromatin accessibility and transcription. Epigenetic conditioning enables prediction of phenomena not encoded in allele sequence, including parent-of-origin imprinting, random monoallelic activity, and X-inactivation. We highlight a promising application of methylation conditioning by predicting the effects of a structural rearrangement in one rare disease patient case study. In silico motif insertion analysis confirms that MethylSeqNet learns methylation-dependent regulatory grammar, establishing a paradigm for integrating epigenetic information into genomic deep learning with immediate applications in rare disease interpretation.

Indexed as

conditioningCpG methylationepigeneticsgenomic deep learninglong-read sequencingsequence-to-activity

Identifiers

PMID42282607
PMCPMC13252088

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.