My research spans the intersection of genetics, genomics, bioinformatics, and AI. I combine cutting-edge data science with deep biological insights to drive transformative innovation in precision health. Each project showcases my commitment to open, impactful, reproducible science that empowers clinicians and individuals alike.
My PhD focuses on building intelligent agent systems powered by Large Language Models (LLMs) for personalized genomic interpretation. By fusing multi-omics data, retrieval-augmented generation, and explainable AI, I aim to make variant interpretation scalable, interpretable, and clinically actionable. This work sets a new standard for privacy-preserving, human-in-the-loop genomic reasoning.
I develop pipelines that connect genomics, transcriptomics, and phenotypic data, ensuring robust prediction models. By leveraging ontologies and domain-specific embeddings, my frameworks enable holistic views of complex diseases, supporting early diagnosis and precision interventions.
One of my key goals is to design AI models clinicians trust. Using XAI techniques, causal reasoning, and transparent agent workflows, my research ensures that every insight is traceable and understandable. This bridges the gap between black-box AI and critical clinical decision-making.
I am committed to democratizing access to advanced genomic tools and making personalized health insights available to all. By open-sourcing critical components and advocating for ethical, fair AI practices, my work will pave the way for a collaborative, impactful future in precision medicine.
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| Genetic Polymorphisms Associated with Insulin Resistance Risk in Normal BMI Indians: INTS10, LINC01427-LINC00261, SENP2, SLC22A11 |
| Insulin Resistance Risk in Normal BMI Individuals: RNF138, ABCA1, ESRRG-GPATCH2 Gene Polymorphisms |
| Paradigm Shift in Nutritional Science: Using Machine Learning to Predict Macronutrient Requirements |
| Unveiling Genetic Associations: CLDN16, GRID2, NRG3, and CACNG4 Gene Polymorphisms with Insulin Resistance Risk |