Genomics
High‑Throughput Sequencing • Single‑Cell & Spatial Omics • Advanced Molecular Analysis
Genomics Core
The UNT Health Genomics Core provides comprehensive genomic services—from experimental design through sequencing and data interpretation. We support projects across genomics, transcriptomics, epigenomics, and multi‑omics workflows using state‑of‑the‑art sequencing technologies and automated laboratory systems. We strive to enable rigorous, reproducible research for the UNT Health community and external collaborators.
Additional Information
- Project Consultation: Discuss goals, library prep options, sequencing strategies, and budgets.
- Submit Requests via Genomics iLab: View equipment, request services, and coordinate sample drop‑off.
- Sample Submission: Provide raw samples or prepared libraries; staff advise on QC requirements.
- Execution: Library prep → QC → Sequencing → Primary data processing.
- Data Delivery: Direct transfer or Cloud storage for compatible runs.
Please acknowledge the UNT Health Genomics Core in posters, manuscripts, and presentations. Example: “We acknowledge the UNT Health Genomics Core for training and assistance on [workflow/instrument].” If core staff make significant intellectual contributions, please consider co‑authorship.