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The Oncological Data Science (T32 ODSi) Training Program is a two-year predoctoral program that develops skills in biomolecular-anchored cancer data science by integrating bioinformatics, molecular population health, and cancer data science within a strong Huntsman Cancer Institute educational and research environment.
 

The T32 ODSi program requires a mentoring team that includes a computational/data mentor and a mentor from either cancer biology or cancer population sciences (domain expert). See Figure below for the ODSi mentorship model. The list of current T32 ODSi mentors is here.

Program Goal

Prepare young scientists to become data ambassadors and data innovators in the use of cancer data science techniques and methodologies to advance the understanding, prevention, diagnosis, and treatment of cancer.

For more information, contact Aik Choon Tan at Aikchoon.Tan@hci.utah.edu.

Eligibility

  • Full-time 2nd or 3rd year U of U PhD-seeking student who has initiated a research
    program in the laboratory of an ODSi faculty member
  • US citizen or permanent resident, and meet all other NIH eligibility criteria
  • Agree to attend and participate in all program components for the entirety of the program
ODSi T32 Trainee Diagram

Accepts

Predoctoral Only

Important Dates

Applications Open: February 13, 2026
Applications due: August 31, 2026
Funding begins: October 1, 2026

Apply for the Program

Contact Us

Principal Investigators

Yves Lussier Headshot

Yves Lussier, MD, FACMI, FAMIA

Program Coordinator:

Kelly Chanthapanya

Kelly Chanthapanya

Program Coordinator, CRTEC

Trainees

Cohort 2 (2026)

Tessa Bass posing for a photo

Tessa Bass

Tessa’s project aims to develop an integrated computational framework to characterize a novel phenotype known as androgen receptor–indifferent (ARi) prostate cancer. By integrating bulk DNA and RNA sequencing, spatial transcriptomics, digital pathology, multiplexed immunofluorescence, and clinical data, she seeks to create a framework capable of identifying ARi regions within prostate cancer tissue and generating phenotype-specific molecular and spatial characterizations. This work will also investigate the transcriptional programs underlying ARi development and establish clinically relevant correlates associated with the phenotype. Ultimately, she hopes to translate these findings into clinically actionable biomarkers that can guide treatment strategies for patients with ARi prostate cancer.

Tessa's Mentors: 

Samuel Coleman posing for a picture

Samuel Coleman

Samuel Coleman develops computational and statistical methods for analyzing single-cell genomic data, with a particular focus on CRISPR-based perturbation experiments and single-cell DNA sequencing technologies. His research aims to improve the resolution and scalability of approaches for characterizing cellular heterogeneity, lineage relationships, and genome editing outcomes at the single-cell level. By integrating novel computational methodologies with high-throughput sequencing data, he seeks to better understand mechanisms underlying cancer progression, therapeutic response, and immune regulation. His long-term interests lie in advancing single-cell technologies and applying them to oncology, immunotherapy, and precision medicine.

Samuel's Mentors: 

Cohort 1 (2025)

Sophie Huebler

Sophie Huebler

Sophie’s research focuses on accelerating the discovery of microbiome-based therapies for patients undergoing allogeneic stem cell transplants, who are at high risk of developing Graft-versus-Host Disease (GVHD). To overcome inconsistent findings from small studies and inadequate statistical methods, Sophie is building a large harmonized multi-study database and applying a novel Bayesian meta-analysis framework. This approach will enable robust identification of microbial signatures that drive GVHD, guiding targeted therapies to improve patient survival.

Sophie’s Mentors: 

Elena Nazarenko

Elena Nazarenko

Elena's project aims to develop new strategies for identifying effective therapies for rare cancers such as acral melanoma, where treatment options remain limited. Using a Bayesian variable selection framework, she will analyze high-dimensional multi-omics data to propose rational combination therapies and construct graphical models to infer cell–cell interactions within the tumor microenvironment. To maximize impact, she will also design interactive visualization tools to share our findings openly with researchers and clinicians.

Elena’s Mentors: 

Carrie Vanty

Carrie Vanty

Carrie’s project involves mathematical modeling and data analysis to study the Hedgehog pathway, a gene regulatory network that is essential for vertebrate development.  Mutations within the pathway are associated with various cancers, such as medulloblastoma, the most common pediatric brain cancer. In collaboration with Dr. Adler and Dr. Myers, Carrie aims to use data-driven modeling to uncover influential genes involved in medulloblastoma and investigate their role in the Hedgehog pathway.

Carrie’s Mentors: