I am a Postdoc researcher at UChicago in the
Madduri group at ANL, collaborating with the
Odunsi group.
My research explores the human genome in complex disorders and builds tools along the way.
My PhD focused on the role of tissue-specific transcript variants in health and cancer,
leveraging large language models (LLMs) to decode the regulatory logic of tissue specificity.
My work bridges bioinformatics, genomics, and AI to address critical challenges in precision medicine.
Research
TransTEx — tissue-specificity scoring
A statistical method that groups the human transcriptome into distinct expression
classes — tissue-specific, tissue-enhanced, widespread, lowly expressed, and null.
Presented at the Great Lakes Bioinformatics Conference (ISCB), Pittsburgh, PA.
A deep-learning framework that learns the DNA regulatory grammar behind tissue-specific
promoters across species, using interpretable attention to surface the motifs and
transcription-factor families that drive specificity. Published in
NAR Genomics and Bioinformatics.
Extends TransTEx to tumors, contrasting normal and cancer expression groups to nominate
transcript-level biomarkers — oncogenes, tumor suppressors, and cancer-testis antigens —
with applications in solid-tumor clustering and pan-glioma classification.
PGViS: Personal Genome Variant interpretation Score for lung cancer genomes
A framework that quantifies individual non-coding germline regulatory risk in non small cell lung cancer (NSCLC).
Each signal is weighted by cohort prevalence which are aggregated into a single ancestry matched, reference normalized score per patient.
Oct 2026Received BSD Career Advancement for Postdocs (CAP) Travel Award: Conference travel support for Supercomputing 2026 to present a poster on agentic approaches in cancer at the CAFCW Workshop.
Sep 2026Frames of Research: The UChicago Postdoc Research Showcase (National Postdoc Appreciation Week 2026) [Poster or Website]
Sep 2026Received BSD Small values grant: Conference support ASHG 2026 to present a poster on drug targets for splice site affecting mutations.