The Genetic and Molecular Epidemiology Laboratory (GMEL) provides a broad range of genomics and proteomics solutions from high-throughput DNA/RNA extraction to sample quantitation and quality assessment, microarray-based experiments (genotyping, gene expression, methylation), next-generation sequencing (exome, RNA, custom target, low-pass whole-genome), multiplexed protein biomarker assays, and many other services. Our laboratory specializes in large-scale population genetic studies, and as such, is capable of handling project sizes ranging from single samples to > 10,000 samples. Additionally, we provide support for experimental design considerations, bioinformatics and statistical analyses, and interpretation/ reporting of results.
Located in the core of downtown Hamilton at the David Braley Cardiovascular and Stroke Research Institute, the GMEL directed by Dr. Guillaume Paré is fully equipped to perform cutting-edge genomics experiments. The GMEL possesses a broad variety of instrumentation (QIAsymphony, BioAnalyzer, Fragment Analyzer, Gene Titan array scanner, Illumina iScan, 2 Ion Torrent S5XL Sequencers, BioNano Genomics Irys System, Thermofisher ViiA7 RT-PCR System, QuantStudio 3D Digital PCR System, Pyromark Q24 instrument, BioMark HD System, Bio-Plex Luminex Multiplex assays, Olink panel assays) as well as the necessary bioinformatics infrastructure (10 dedicated servers) to process large genomics projects at reasonable turnaround times.
DNA and RNA extraction from a wide variety of materials including: buffy coat, whole blood, dried blood spots, FFPE, saliva, tissue samples and dried blood spots. Quantitation using Nanodrop, Picogreen, or Qubit assay. Fragment analysis using Bioanalyzer or Fragment Analyzer instruments.
Full complement of Thermofisher (formerly Affymetrix) genotyping arrays including: Precision Medicine Research Array and UK Biobank Array
Custom Axiom (formerly Affymetrix) genotyping – 300-200,000 marker density
Genotyping (1-96 SNPs) - Taqman and SNPtype assays using ViiA7 and BioMark instruments.
Full complement of Illumina genotyping arrays including: Global Screening Array, CoreExome, Omni2.5 arrays with semi-custom (add-on) content available for most arrays
Custom Infinium genotyping - 3-90K or 90,001-700K marker density
Array based methylation using Illumina MethylationEPIC Array
Targeted methylation using Qiagen Pyromark Q24
qPCR based methylation profiling
Full complement of array based gene level expression profiling and whole transcriptome analysis including ClariomS and Clariom D microarrays by Thermofisher (Affymetrix).
qPCR based gene expression analysis.
See “Next-Generation Sequencing” section for sequencing based options.
Ion Torrent sequencing using S5XL instruments:
Pre-designed and custom panel development for targeted sequencing using Ampliseq technology
Whole Exome Sequencing using Ion Ampliseq Exome library preparation and Ion Torrent sequencing technology
Low pass Whole Genome Sequencing
Sequencing based gene level expression profiling using Ion Ampliseq Transcriptome and whole transcriptome analysis using Ion Total RNAseq
See “Expression” section for array based options.
Whole Molecule Sequencing, long range genomic mapping, structural variations
GeneChips Thermofisher (formerly Affymetrix) including: Genome-Wide Human SNP Array 6.0 and OncoScan CNV Assay
Digital PCR for rare allele detection, precise copy number variation and low‐level fold change of gene expression
Certified service provider of Olink assay - 92 biomarkers per panel with 12 panels covering all major disease areas including the following: Cardiometabolic, Neurology, Oncology, and Inflammation. Validated for EDTA serum and plasma. Other sample types possible. <1µl of sample per panel required for testing.
Luminex multiplex biomarker testing – 1-96 analytes
We offer flexible bioinformatics support for all genomics services with regards to:
David Braley Cardiac, Vascular and Stroke Research Institute
30 Birge Street, Room 1-10 C4 North 207
Hamilton ON L8L 0A6