Abstract

This systematic review investigates the transformative role of big data technologies in biomedical research, analyzing 40 peer-reviewed articles published between 2010 and 2023. The review specifically explores advancements in next-generation sequencing (NGS), multi-omics approaches, machine learning, and artificial intelligence (AI), all of which have significantly enhanced the understanding of complex biological systems and diseases. NGS has emerged as a key tool in personalized medicine, enabling rapid and cost-effective genome sequencing that has facilitated the identification of genetic mutations and biomarkers associated with various diseases, particularly in oncology. Of the 40 studies reviewed, 12 focused on the integration of multi-omics data—genomics, transcriptomics, proteomics, and metabolomics—to provide a comprehensive view of biological processes. These multi-omics approaches have been instrumental in identifying biomarkers for disease progression and response to treatments, offering new avenues for drug development and precision medicine. Additionally, 15 studies highlighted the growing application of machine learning and AI algorithms in managing and analyzing vast biomedical datasets. These tools are now critical in uncovering hidden patterns within large datasets, predicting disease outcomes, and improving the accuracy of clinical decision-making. However, 10 studies emphasized ongoing challenges related to data storage, privacy concerns, and the lack of standardized data formats, which hinder effective data sharing across institutions. Despite these challenges, the integration of AI, IoT devices, and big data analytics is paving the way for more personalized, real-time healthcare monitoring and treatment solutions. This review concludes that while significant advancements have been made, further efforts are required to address the ethical and technical barriers that limit the full potential of big data technologies in biomedical research.

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