Vanderbilt freshmen and sophomores: please email Dr. Kroncke below.
No other positions are currently open. Prospective collaborators are welcome to get in touch.
Variant-level disease probability with explicit uncertainty; extending to individual clinical risk.
Deep mutational scanning, calibrated automated patch clamp, quantitative proteomics.
Patient-derived and CRISPR-edited lines to test polygenic background and drug response.
LLM extraction from the literature with source-level traceability and ClinGen-style consensus.