ArticleInternational journal of molecular sciences2025
Prediction of Enhancer RNAs in Chicken Genome.
Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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Who cites it
1 citing paper in PubMed.
- Advances in Poultry RNA-Omics Research: Technologies, RNA Information Layers, and Applications in Complex Traits.Animals : an open access journal from MDPI · 2026Review
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Authors and funding
6 authors.
Funding
Abstract
Enhancer RNAs (eRNAs) play an important role in transcriptional regulation and serve as key intermediates linking genomic enhancers to their target genes. Although ongoing efforts aim to annotate enhancers in the chicken genome, the current understanding of avian enhancers remains less developed compared to that of mammals. We utilized CAGE-seq data from chicken tissues obtained through the "Genetic Technologies in Poultry" project to predict enhancers in the chicken genome. Preliminary predictions focused on non-coding regions exhibiting bidirectional transcription, which were subsequently validated using explicit Markov models and refined with hidden Markov models. To assess sequence family homogeneity, we developed a method based on Euclidean distances between explicit Markov model matrices. Our analysis revealed that the proportion of enhancer-associated DNA in chicken is approximately similar to that observed in mammals, encompassing 9.29% of the entire chicken genome, roughly similar to the estimate made by the ChickenGTEx project. A relatively small number of them (12,242 enhancers) were significantly expressed among all tissues. Notably, more than half of the enhancer DNA overlapped intronic regions. Additionally, based on the bimodal distribution of enhancer lengths combined with the homogeneity of their Markov models, we identified a class of long enhancer elements which we hypothesize to be absent in mammals.
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Registered trials
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