CV
Curriculum Vitae
A summary of my experience and training. The full CV is available as a PDF.
Experience
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Dec 2025 – Present
Associate Manager, Genomics & Health Data Mining
Statistical genetics and machine learning for target discovery: association testing, fine-mapping and colocalization across large exome and proteomics cohorts, phenome-wide analyses for efficacy and safety, and portfolio-level views of the human genetic evidence behind targets across therapeutic areas.
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Summer 2025
PhD Intern, Neuroscience & Ophthalmology TA Genetics
Worked on linking GWAS loci to drug-response mechanisms in the Tahoe-100M single-cell perturbation atlas, asking how germline variants shape cellular responses to pharmacological intervention.
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2020 – 2025
Graduate Researcher, Computational Biophysics & Neurobiology
University of South Florida · Ullah Lab
Built biophysical models of presynaptic Ca²⁺ signaling and single-cell multi-omics pipelines to map cell-type-specific mechanisms of synaptic dysfunction in Alzheimer's disease. Led the lab's genomics subgroup and mentored three trainees.
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Summer 2022
Research Intern, Human Multi-omics
Developed interpretable deep-learning pipelines (scArches / expiMAP) for reference mapping of single-cell data, informing target prioritization for Alzheimer's and Parkinson's disease programs.
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2021 – 2022
Bioinformatics Research Student
University of South Florida · Uversky Lab
Studied intrinsic protein disorder in Ebola and Marburg virus proteins and its implications for virulence.
Education
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2019 – 2025
PhD, Applied Physics
University of South Florida
Computational Biophysics & Neurobiology
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2019 – 2023
MSc, Applied Physics
University of South Florida
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2012 – 2017
BSc, Applied Physics (Electronics)
University of Lagos
First Class Honours · Best Graduating Student
Honors
- Trainee Professional Development Award, Society for Neuroscience, 2024
- Best Graduating Student, BSc Applied Physics, University of Lagos, 2017
Toolkit
- Languages
- Python, R, Bash, SQL, MATLAB, Fortran
- Statistical genetics
- Common and rare-variant association (GWAS, exome burden), LD, fine-mapping, colocalization, PheWAS
- Genomics
- scanpy, scvi-tools, scArches, scVelo, hdWGCNA, SCENIC+, ArchR, squidpy, GSVA
- Machine learning
- PyTorch, TensorFlow/Keras, scikit-learn, statsmodels
- Modeling
- ODE/stochastic biophysical models, network biology, statistical modeling
- Compute
- HPC, CUDA, mpi4py, AWS SageMaker, GCP, Terra, Docker, Git