Genomics Drives Precision Medicine and Diagnostics
Received Date: Oct 01, 2025 / Published Date: Oct 29, 2025
Abstract
This review explores the transformative impact of genomic sequencing technologies across diverse clinical and research domains. Whole genome sequencing, long-read sequencing, and single-cell transcriptomics are advancing our understanding of rare diseases, cancer, and cellular heterogeneity. Large-scale projects highlight genomic medicine’s potential, despite challenges in data interpretation. Epigenomic sequencing, precision oncology, non-invasive prenatal testing, pharmacogenomics, and microbial sequencing all represent critical applications. These innovations are revolutionizing diagnostics, personalizing therapies, and enhancing public health surveillance, underscoring genomics’ central role in modern healthcare and biomedical research.
Keywords: Whole Genome Sequencing; Precision Oncology; Long-Read Sequencing; Single-Cell Transcriptomics; Pharmacogenomics; Non-Invasive Prenatal Sequencing; Microbial Genomics; Rare Diseases; Epigenomics; Clinical Diagnostics
Citation: O’Connor L (2025) Genomics Drives Precision Medicine and Diagnostics. jabt 16: 807. Doi: 10.4172/2155-9872.1000807
Copyright: © 2025 Liam O’Connor This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
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