Evidence map›Paper›PMID 41189647›Full record

ArticleNAR genomics and bioinformatics2025

Sequence-based chromatin activity modeling and regulatory impact prediction of genetic variants in farmed animals using deep learning.

Dat Thanh Nguyen, Tim Martin Knutsen, Simen R Sandve, Sigbjørn Lien, Lars Grønvold

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

5 authors.

Dat Thanh NguyenCentre for Integrative Genetics, Faculty of Biosciences, Norwegian University of Life Sciences, 1432 Ås, Norway.ORCID https://orcid.org/0000-0003-3852-9578
Tim Martin KnutsenAquaGen AS, P. O. Box 1240, NO-7462 Trondheim, Norway.
Simen R SandveCentre for Integrative Genetics, Faculty of Biosciences, Norwegian University of Life Sciences, 1432 Ås, Norway.
Sigbjørn LienCentre for Integrative Genetics, Faculty of Biosciences, Norwegian University of Life Sciences, 1432 Ås, Norway.
Lars GrønvoldCentre for Integrative Genetics, Faculty of Biosciences, Norwegian University of Life Sciences, 1432 Ås, Norway.ORCID https://orcid.org/0000-0001-5404-4285

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Noncoding genomic variations are crucial for the genetic regulation of traits; however, their functional impact in farmed animals remains underexplored due to limited genomic resources and the absence of tailored computational tools. Here, we present a deep learning-based framework that utilizes functional genomic data to generate genome-wide predictions of the regulatory impact of noncoding variants in cattle, chicken, pig, and Atlantic salmon. By leveraging chromatin profiles such as assay for transposase-accessible chromatin, DNase I hypersensitive site, and chromatin immunoprecipitation sequencing data, we train and optimize separate deep networks for each species, achieving robust sequence modeling accuracy specific to each. Motif analysis confirms that the models capture regulatory grammar, while

Indexed as

Animals, DomesticChromatinDeep LearningGenetic VariationAnimalsCattleChickensChromatin Immunoprecipitation SequencingQuantitative Trait LociSalmo salarSwineChromatin

Identifiers

PMID41189647
PMCPMC12582021

What OpenQuestion holds

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Registered trials

None linked

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.