Image-based DNA sequencing encoding for detecting low-mosaicism somatic mobile element insertions

Active mobile elements in the human genome can create novel mobile element insertions (MEIs) in somatic tissues. Detection of somatic MEIs, particularly those with low mosaicism, remains a significant challenge due to sequencing artifacts and alignment errors. Existing methods lack sensitivity or require biased manual inspection. Here we present RetroNet, a deep learning algorithm that encodes sequencing reads into images to identify somatic MEIs with as few as two reads. Trained on diverse datasets, RetroNet outperforms previous methods and eliminates the need for manual examinations. RetroNet achieves high precision (0.885) and recall (0.579) on a cancer cell line, detecting insertions in just 1.79% of cells. RetroNet is also effective for degraded DNA, like circulating tumor DNA. This tool is applicable to the rapidly generated short-read sequencing data and has the potential to provide further insights into the functional and pathological implications of somatic retrotranspositions.

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Publication Details

Journal
Nature Communications
Published
2025-10-16
DOI
https://doi.org/10.1038/s41467-025-64237-w
Primary Topic
Chromosomal and Genetic Variations
Type
article
Field-Weighted Citation Impact
0.00

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article

Image-based DNA sequencing encoding for detecting low-mosaicism somatic mobile element insertions

Zhipeng Gao, Xiaowei Zhu, Zequan Chen, Eunjung Alice Lee et al.
Nature Communications
Chromosomal and Genetic Variations
article

Image-based DNA sequencing encoding for detecting low-mosaicism somatic mobile element insertions

Zhipeng Gao, Xiaowei Zhu, Zequan Chen, Eunjung Alice Lee, Miaomiao Tan, Junseok Park, Zhinan Lin, Haonan Zhou, Zhenzhen He
article en

Abstract

Active mobile elements in the human genome can create novel mobile element insertions (MEIs) in somatic tissues. Detection of somatic MEIs, particularly those with low mosaicism, remains a significant challenge due to sequencing artifacts and alignment errors. Existing methods lack sensitivity or require biased manual inspection. Here we present RetroNet, a deep learning algorithm that encodes sequencing reads into images to identify somatic MEIs with as few as two reads. Trained on diverse datasets, RetroNet outperforms previous methods and eliminates the need for manual examinations. RetroNet achieves high precision (0.885) and recall (0.579) on a cancer cell line, detecting insertions in just 1.79% of cells. RetroNet is also effective for degraded DNA, like circulating tumor DNA. This tool is applicable to the rapidly generated short-read sequencing data and has the potential to provide further insights into the functional and pathological implications of somatic retrotranspositions.

Nature CommunicationsVol. 16(1)
Broad Institute (US), Boston Children's Hospital (US), Harvard University (US), City University of Hong Kong (HK), Lemuel Shattuck Hospital (US), Zhejiang Shuren University (CN), Zhejiang University (CN)
National Science Foundation, Yale University, City University of Hong Kong, National Natural Science Foundation of China, Zhejiang University, Zhejiang Shuren University, Innovation and Technology Fund
Openalex Percentile: Top 78%
Chromosomal and Genetic Variations
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