Genomics and Data Science & Computing Core

Genomics Core – Advanced Research Infrastructure

The UNT Health Genomics Core provides comprehensive support for high-throughput sequencing and computational genomics, enabling rigorous and reproducible research across diverse biological systems.

 

Research Applications

  • Short-read sequencing for genome and transcriptome analysis
  • Long-read sequencing for structural variation and complex assemblies
  • Spatial transcriptomics for tissue-level gene expression mapping
  • Single-cell sequencing for cellular heterogeneity studies

Instrumentation

  • Illumina NextSeq 2000 – High-throughput short-read sequencing
  • PacBio Vega – Long-read sequencing for high-fidelity assemblies
  • 10x Genomics Chromium X – Single-cell and multi-omics workflows
  • Visium CytAssist – Spatial transcriptomics platform
  • Agilent TapeStation 4200 – Nucleic acid quality assessment
  • Bio-Rad qPCR system and Digital PCR platform – Quantitative analysis

Our facility is committed to supporting investigators through all stages of the workflow — from sample preparation to sequencing and data interpretation — ensuring high-quality results for publications and grant-funded projects.

 

Location

Genomics Core, RES-126

UNT Health

3500 Camp Bowie Blvd

Fort Worth, TX 76107

 

Contacts

Name Role Phone Email Location
TBD
Genomics Core Manager
 

 
Researchcorelabs@unthealth.edu
 
RES-126
 
Janak Sunuwar, PhD
Data Science and Computing Core Manager
 
402-810-4232
 
Janak.Sunuwar@unthealth.edu
 
EAD 124
 

Service list


Search available services: View: by category alphabetically
Epigenetic services (5)
MiSeq Sequencing (8)
NextSeq Sequencing (1)
TapeStation 4200 (1)
Biological Material Testing (8)
Extractions (2)
PCR-Based Assay: Digital PCR / Quantitative PCR / Realtime PCR (3)