AI and automation are transforming evidence-based medicine by enabling efficient, precise, and scalable insights from vast biomedical data. At Nucleati, we leverage advanced AI technologies to extract critical information from scientific literature, clinical datasets, and genomic resources, accelerating the identification and interpretation of genetic variants. Our automated workflows streamline evidence curation and ensure that healthcare professionals can access reliable, up-to-date knowledge for improved diagnostics and personalized treatment. With AI-driven innovation, we empower clinicians and researchers to make data-backed decisions, bridging the gap between discovery and actionable care.
Adenine AI is a comprehensive portal providing access to curated data generated through Nucleati's advanced AI and automation pipelines. Designed for a wide variety of users, including medical practitioners leveraging genetics for patient care, genetic counselors, medical geneticists, researchers, and others, it offers meticulously collected, normalized, and organized data. Adenine AI empowers users to explore the genetic basis of disease, classify variants, uncover gene-disease relationships, and advance personalized medicine with evidence-driven insights.
VarSy is a powerful tool that delivers fast and accurate synonyms for genetic variants, utilizing up-to-date transcripts and the CHM13 reference assembly. By harmonizing variant nomenclature across the latest genomic resources, VarSy ensures precise and reliable data integration for research and clinical applications. This indispensable tool enables researchers, clinicians, and geneticists to efficiently identify and aggregate variant information, supporting advanced AI-driven solutions in variant-centered genetics. With VarSy, users can seamlessly navigate the complexities of genomic data and drive innovation in personalized medicine.
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