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Adib Hossain

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Review Open access Aug 2026

Integrating Artificial Intelligence with Global Genomic Resources: A Narrative Review of Implications for Precision Medicine

Purpose This review aimed to explore how artificial intelligence can be integrated with global genomic resources and to examine its implications for advancing precision medicine, with particular attention to population diversity, predictive modeling, and clinical translation. Methods A narrative review design was adopted, drawing on literature from major databases and supplementary search sources including PubMed, Scopus, Web of Science, IEEE Xplore, Embase, and Google Scholar. Studies were selected based on relevance to artificial intelligence applications in genomic data analysis and precision medicine. Key information from included studies was extracted using a structured narrative extraction framework and synthesized thematically to identify key patterns and emerging insights. Results A total of 54 studies were included in this review. The synthesis identified five recurring application areas: genomic data integration, variant and disease association detection, disease susceptibility and risk prediction, treatment response prediction, and clinical decision support. Findings indicate that artificial intelligence can support the integration and analysis of multi-omics data, support the identification of genetic variants and disease associations, and improve predictive modeling for precision medicine. Incorporating diverse population data was also reported to improve model generalizability and reduce bias. However, challenges related to data standardization, interoperability, ethical governance, overfitting in small or biased cohorts, limited prospective clinical validation, reproducibility, and clinical implementation remain significant barriers. Conclusion The integration of artificial intelligence with global genomic resources holds substantial promise for advancing precision medicine by enabling more accurate, inclusive, and individualized precision medicine. However, this promise should be interpreted cautiously because many AI genomic models remain dependent on retrospective datasets, limited external validation, and variable reproducibility.

Towsif Alam, Koushik Saha, M. K. K. Rony et al. · 0 citations
Review Open access Jul 2026

Big Data in Cancer Genomics: Computational Foundations and Emerging Pathways for Precision Oncology

This review aims to explore the computational foundations of big data in cancer genomics and examine emerging pathways that support precision oncology and personalized cancer care. A narrative review approach was adopted to synthesize evidence from PubMed, Scopus, Web of Science, and IEEE Xplore. The literature search was conducted between January 10 and February 25, 2026, and 68 relevant studies were included in the final synthesis. Relevant studies were selected on the basis of their focus on computational methods, data integration strategies, and artificial intelligence (AI) applications in cancer genomics. Extracted data were organized into thematic categories and analyzed using an iterative synthesis framework. The findings indicate that high‐throughput sequencing and multi‐omics technologies have significantly expanded the volume and complexity of cancer‐related data. Advanced infrastructures, including cloud platforms, improve storage and access but raise privacy and interoperability concerns. Machine learning and AI support tumor classification, biomarker discovery, and treatment prediction. Integrative multi‐omics enhances biological insight and predictive accuracy. However, challenges such as data heterogeneity, limited model generalizability, and gaps in clinical integration remain. Big data in cancer genomics offer substantial potential to advance precision oncology by enabling more accurate and personalized treatment strategies. However, overcoming technical, ethical, and infrastructural barriers is essential to ensure effective translation into clinical practice and equitable healthcare outcomes.

Nur Vanu, Nur Mohammad, Fahad Ahmed et al. · 0 citations