The future of NGS in neonatal disorders looks promising with ongoing advancements in technology and bioinformatics. Potential developments include: - Whole Genome Sequencing: Becoming more accessible and affordable for routine clinical use. - Integration with Other Technologies: Combining NGS with other diagnostic tools for a more comprehensive approach. - Expanded Genetic Databases: Improving the accuracy of variant interpretation through larger and more diverse genetic databases. - Personalized Neonatal Care: Further tailoring treatments and interventions based on individual genetic profiles.
