Next Generation Sequencing
Download our Quick Guide to Getting Started with CHGI - NGS.
From transcriptome to whole-genome sequencing, CHGI delivers exceptional data quality, industry-leading throughput, and cost-efficient sequencing at scale.
The Centre for Health Genomics and Informatics (CHGI) is a full service core infrastructure facility offering next generation sequencing (NGS) 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 we 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 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.
Download our Quick Guide to Getting Started with CHGI - NGS.
Please arrange a meeting to discuss sample requirements, replicates, and sequencing options before beginning new NGS projects.
Services are available for assessing DNA and RNA samples or user-prepared NGS libraries.
We offer sample prep services for genomic, metagenomic, transcriptomic, and small RNA sequencing as well as targeted sequencing via amplicons or hybridization-capture methods.
CHGI uses industry-standard sequencing and analytical platforms in a dedicated sequencing laboratory to deliver high-quality data.
Resources for data analysis and storage
Compute resources in our private server room and other locations.
Multi-petabyte data storage on disk and tape.
Accurate, comprehensive, and efficient secondary analysis of next generation sequencing data.
Bioinformatics staff who can provide additional fee-for-service assistance.
Find information on data storage and bioinformatics services here.