ArticleMethods in molecular biology (Clifton, N.J.)2025
Deep Genomics: Deep Learning-Based Analysis of Genome-Sequenced Data for Identification of Gene Alterations.
Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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.
Who cites it
2 citing papers in PubMed.
- Integrating mathematical modelling and artificial intelligence to combat emerging viral syndemics: A systematic review.New microbes and new infections · 2026Review
- Harnessing Deep Learning Models for Guide RNA Optimization and Off-Target Prediction in CRISPR Systems.Biotechnology journal · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The convergence of next-generation sequencing and advanced computational methods has reshaped genomic analysis by enabling unprecedented volumes of molecular data to be generated and scrutinized. This chapter surveys the rapidly evolving landscape of deep genomics, highlighting how breakthroughs in deep learning frameworks-such as Convolutional Neural Networks, Recurrent Neural Networks, Transformers, and Graph Neural Networks-allow researchers to detect, characterize, and interpret complex genetic alterations. We begin by illustrating the progression from traditional bioinformatics to contemporary neural architectures capable of identifying fine-grained molecular signals. CNNs excel at discerning localized sequence motifs, RNNs capture dynamic expression patterns in sequential data, Transformers unveil long-range dependencies crucial for pinpointing regulatory variants, and GNNs trace systemic gene-gene and protein-protein interactions, clarifying how single mutations can ripple throughout biological networks.A central theme is the integration of diverse omic layers-encompassing epigenomic, transcriptomic, and proteomic profiles to offer a more comprehensive perspective on genomic regulation. While this approach amplifies the detection power for pathogenic variants and hidden biomarkers, it also poses significant methodological hurdles related to data harmonization and interpretability. Techniques such as saliency mapping, SHAP analysis, and gradient-based CAM illuminate the internal logic of these deep models, strengthening reliability in clinical diagnostics and fueling mechanistic insights in research settings. Beyond methodological innovations, the chapter underscores data privacy, systematic bias mitigation, and explainability protocols as foundational elements for the safe and ethical use of deep genomics tools in clinical and research environments. Regulatory compliance and transparent communication of model outputs are indispensable for cultivating public trust and ensuring equitable access to genomic medicine.Looking ahead, emerging technologies such as secure multi-institutional data analysis protocols, federated learning, and potential quantum computing applications offer promising avenues for scaling analysis to ever-larger datasets without jeopardizing patient privacy. As these advancements merge with more refined models, precision medicine stands to benefit from unprecedented accuracy in variant interpretation, timely disease diagnosis, and effective therapeutic strategies. By integrating cutting-edge computational methods with robust ethical frameworks, deep genomics is poised to transform our understanding of genetic variation and its implications for human health.
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Identifiers
40553343What OpenQuestion holds
Registered trials
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.