Next Generation Sequencing
Download our Quick Guide to Getting Started with CHGI - NGS.
Centre for Health Genomics and Informatics
From transcriptome sequencing to whole-genome sequencing and everything in between, the NovaSeq 6000 is a highly robust system capable of producing high-quality data at competitive $/Gb prices.
The Centre for Health Genomics and Informatics (CHGI) is a full service core infrastructure facility offering Sanger and Next-Generation DNA sequencing services and bioinformatics support to researchers across the University of Calgary and other research institutions.
Researchers need only submit isolated genomic DNA or total RNA and the Centre will perform all the following steps, from NGS library preparation through to generation of lists of variants or expressed genes. A wide variety of NGS applications, from single cell sequencing to metagenomics, are supported.
We aim to build the technological, bioinformatics and human resource capacities required to support the research and health care needs of our university and province, in alignment with Precision Medicine and Precision Health strategies.
Learn more about how CHGI delivers trusted, high-impact sequencing services with expert support, advanced technology, and a proven track record in Canadian genomics research. Explore our highlights below.
Consulting and Project Planning
Please arrange a meeting to discuss sample requirements, replicates, and sequencing options before beginning new NGS projects.
Analytical Services
Services are available for assessing DNA and RNA samples or user-prepared NGS libraries.
Library Preparation Services
We offer sample prep services for genomic, metagenomic, transcriptomic, and small RNA sequencing as well as targeted sequencing via amplicons or hybridization-capture methods.
Next-Generation Sequencing Services
Next-gen sequencers for short- and long-read sequencing.
Sanger Sequencing and Fragment Analysis
Automated capillary electrophoresis services for Sanger DNA sequencing and size separation of fluorescently-labelled fragments
Sanger DNA Sequencing
Economy and Full Service options for up to 700 bp in length.
Genetic Fragment Analysis
Automated multicolour fluorescent analysis of PCR-based DNA fragments.
dnaLIMS
Our dna Laboratory Information Management System (dnaLIMS) is hosted on a secure server and can only be accessed by managed computers or VPN access if working remotely. We still extend our services to external customers. Please contact us for assistance
Bioinformatics and IT
Resources for data analysis and storage
High-Performance Computing
Compute resources in our private server room and other locations.
Data Storage
Multi-petabyte data storage on disk and tape.
Galaxy Server
Secure access to data and pre-configured workflows.
Bioinformaticians
Bioinformatics staff who can provide additional fee-for-service assistance.
Find information on data storage and bioinformatics services here.