Bioinformatician at the Oklahoma Medical Research Foundation — statistical genetics, GWAS and fine-mapping, reproducible HPC pipelines, and tools that make analysis easier to trust.
I love connecting with different people! Feel free to reach out and say hi!
- Statistical genetics — GWAS, fine-mapping (SuSiE, FINEMAP, COJO), LD, imputation, local ancestry
- Pipelines on HPC — Snakemake + SLURM workflows that scale from one locus to the whole genome
- Sequence analysis — alignment statistics, Sanger QC, VCF harmonization
- Research tooling with AI — provenance tracking and remembering what worked, so analyses can be reproduced and reused
🔭 LYNXgwasLocal GWAS visualization and fine-mapping platform: loci, rsIDs, LD, a full fine-mapping suite and an interactive Manhattan / LD / gene-track viewer — all in your browser. 
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🕸️ SciWeaveEverything your analysis produces, woven into one provenance network with the data, pipelines, parameters and scripts behind it. 
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🧠 brainnyRemembers how you work with AI — captures the techniques, precautions and solutions you invent in passing so you can reuse them. 
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💞 myGeeKyFind GitHub people who share your research — and will actually follow you back. Your CV, repos, ORCID & Google Scholar papers → people and projects worth your time. 
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🌀 crazyAIThe impossible, disguised as possible and true — an AI builds on one deliberately mutated rule with full mathematical rigour, a fresh session checks it, and a judge measures the result. 
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📚 SciLibraManage and organize your scientific PDF articles on mobile and desktop — a pocket library for researchers, students and academics. 
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Sequence analysis · R package
R package for sequence alignment, descriptive analysis and visualization of the results. 
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Sanger QC · Identification
Sanger chromatogram QC, forward/reverse consensus assembly and NCBI identification. 
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Haplotypes · Trait association
Haplotype analysis linking LD-based SNP haplotypes to variation in traits. 
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