- January 30, 2012
Identifying structural variation - January 25, 2012
Autism Speaks - RFA release
- November 29, 2011
9th Annual Affymetrix User Group Meeting -
December 8, 2011
Introducing the NEW Database of Genomic Variants!
The Centre for Applied Genomics provides project support to hundreds of investigators involved in local, nation-wide and international research initiatives. This support includes laboratory experimentation, statistical analysis, and comprehensive bioinformatics support, including large-scale genome comparisons, algorithm and tools development, and database curation, annotation and hosting. For a list of databases hosted by TCAG, please see the TCAG Databases page. Computational support is provided by the Centre for Computational Biology. Major funding for The Centre for Applied Genomics is provided by the Government of Canada through Genome Canada and the Ontario Genomics Institute (OGI-033).
TCAG Bioinformatics Tools
- Genescript Annotation Pipeline
- Generalized Biological Database Platform Based on XRT
- eFISH - an in-silico FISH simulation tool
Supported Genome Canada Large-Scale Projects
For a description of Genome Canada and its activities, please see the Genome Canada and Ontario Genomics Institute websites.
- Structural and Functional Annotation of the Human Genome for Disease Study
- Autism Genome Project
- The Contribution of Genetic Modulators of Disease Severity in Cystic Fibrosis to other Diseases with Similarities of Clinical Phenotype
- Integrative Biology
- The Dynactome: Mapping Spatio-Temporal Dynamic Systems in Humans
- Identification of Genetic Pathways that Regulate the Survival and Development of Cancer and Cancer Stem Cells
- Genome-Environment Interactions in Type 1 Diabetes
- Canadian Barcode of Life Network
- Strengthening the Role of Genomics and Global Health
- North American Conditional Mouse Mutagenesis Project: High Throughput Mammalian Functional Analysis for the Discovery of Novel Determinants of Human Disease
- Enabling Technologies for Embryonic Stem Cell Functional Genomics
Specific Diseases and Disorders
TCAG supports research into a wide variety of genetic diseases and disorders. Information, study consent forms and other materials can be found here. Study participants are contacted directly by study investigators, who will help to explain which of these forms are relevant to each individual participant.
Genetics and Genomics of Autism
- Autism Genome Project
- On Line Resource for parents with a child recently diagnosed with Autism Spectrum Disorder
- 2011 Autism Parent Conference
- International Autism Genome Project
- McMaster - Toronto Autism Project
- background information - a genetic study of Autism
- patient flyer
- consent form
- parental consent for child
- consent form for unaffected individuals
- consent form, Moebius and Autism
- parental consent for child, Moebius and Autism
- screening questionnaire, 7q31 locus
- Canadian Autism Intervention Research Network
Williams-Beuren Syndrome Genetics and Genomics
Russell-Silver Syndrome
Sample Collection & Shipment
Selected Other Supported Initiatives
The Centre for Applied Genomics (TCAG; www.tcag.ca) is a Canadian centre dedicated to supporting genomic applications in biomedical and other areas of genomic research. TCAG maintains Core Facilities for (i) DNA Sequencing and Synthesis, (ii) Cytogenomics and Genome Resources, (iii) Microarray Analysis and Gene Expression, (iv) Genetic and Statistical Analysis, and (v) Biobanking and Databases. These activities are supported by an on-site Administrative Group. The Scientific Director of TCAG is Dr. Stephen Scherer, the Assistant Director is Dr. Richard Wintle, and there are seven Scientific Co-Directors who form the Scientific Management Committee, with expertise in various related disciplines (Drs. Beyene, Bulman, Danska, Osborne, Paterson, Ray and Rommens). TCAG serves as the Genome Canada Science and Technology platform for Ontario, supporting ten large-scale Genome Canada projects, dozens of other large-scale projects and over 500 additional laboratories each year. Facility users represent 28 different countries. Currently, there are approximately 70 staff operating on a multi-million dollar annual budget, including significant grant support from Genome Canada, the Canada Foundation for Innovation (CFI), the Ontario Ministry of Research and Innovation, The Hospital for Sick Children Foundation, and the Wellcome Trust. TCAG services are open to all users in the academic, public, government/NGO or private sectors, on a fee-for-service, cost-recovery basis.
TCAG occupies approximately 12,000 square feet of space in the Toronto Medical Discovery Tower of the MaRS Discovery District, within the Division of Genetics and Genome Biology of The Hospital for Sick Children Research Institute. Samples and processes are tracked within TCAG by the GeoSpiza Finch Suite Laboratory Information Management System (LIMS), which covers the capillary sequencing service, and the Genologics Geneus LIMS, which is being implemented across the other Core Facilities. Each Core Facility is managed by a dedicated Director.
TCAG's Next-Generation Sequencing (NGS) facility operates two Applied Biosystems SOLiD version 3 instruments, one Illumina Genome Analyzer II, and one Roche GS-FLX "Titanium" instrument. This suite of technologies allows for whole-genome de novo or re-sequencing using either single fragments or paired-end approaches, ChIP-sequencing, digital gene expression profiling, and many other applications. An integrated Bioinformatics support team and high-performance computing facility (see below) support this and the other Core Facilities.
For genotyping and conventional capillary sequencing, the centre uses three ABI 3730xl DNA sequencers, one ABI 3100 sequencer, an ABI 7900HT quantitative thermocycler for qPCR analysis and Taqman genotyping, two Illumina BeadStations with an autoloader and associated liquid handling robotics. Custom SNP genotyping by PCR-RFLP or single-base extension is also performed. The Illumina systems are used for genome-wide and targeted genotyping, as well as gene expression, microRNA and methylation analyses. The capillary sequencing facility performs mutation screening, clone verification, and BAC end-sequencing. All of these applications are assisted by automated liquid handling using two Beckman BioMek NX and one BioMek FX robots.
Other microarray technologies include four Affymetrix systems and one Agilent system. The Affymetrix systems are used for both gene expression and genome-wide SNP analysis; one is also upgraded with four-colour MegAllele custom genotyping capability and all are equipped with autoloaders. The Agilent system is used for oligonucleotide array-CGH and other applications, including processing of custom arrays from Agilent or other providers. This microarray facility is by far the most productive in Canada, processing over 5,000 arrays in 2008.
The Cytogenomics Core includes imaging microscopes for applications including Spectral Karyotyping (SKY), mFISH (MetaSystems), metaphase FISH, sequential G-to-FISH mapping (for mapping transgene insertion sites), breakpoint and inversion testing (by interphase FISH) and karyotyping of human, mouse and other species. The facility also performs significant karyotyping and analysis of oncology and stem cell lines.
All of these facilities are supported by the Biobanking and tissue culture facility, which processes blood and fibroblast cultures for DNA, transforms white blood cells to create permanent lymphoblastoid cell lines, and banks white cell pellets. This facility also includes the Ontario Population Genomics Platform (OPGP) collection of over 1,700 cell lines and DNA from healthy controls, as a resource for the scientific community. The Genome Resources facility also supports the other facilities, including genomic clone and cDNA library resources and repositories of human genomic DNA samples. Finally, a DNA synthesis service provides conventional, long and modified oligonucleotides. For users requiring large numbers of oligonucleotides, TCAG also provides a portal for the purchase of oligos from IDT, one of the world's leading suppliers.
The Statistical Analysis Core provides experimental design and power calculations, and a wide variety of analytical approaches, including analysis of genotype, microarray, genomic copy number, epidemiological, and pathway data. TCAG maintains multiple suites of analysis software packages including those from InforSense, SpotFire, Stratagene/Iobion Informatics, Partek, Golden Helix, Ingenuity Pathways Analysis, and a variety of open-source and in-house developed tools. These are also available for clients to use on site for their own data analysis. The Bioinformatics team is active in developing new analytical algorithms and assisting in genome mapping and assembly, annotation, and project design, and is responsible for maintaining TCAG's databases, including the Database of Genomic Variants (http://projects.tcag.ca/variation).
In order to support all data generation, storage, analysis and bioinformatics activities associated with the Centre's activities, TCAG has a variety of computing hardware, including turnkey workstations controlling lab instrumentation, personal and analytical workstations (including several multi-core machines for microarray analysis), web and database servers, and the High-Performance computing Facility (HPF). This cluster consists of symmetric-multi-processing (SMP) computational nodes, and now includes nearly 1,200 predominantly Intel Xeon quad-core processors, three Terabytes of RAM, and over 50 Terabytes of disk space for high throughput computational, bioinformatic and genomic research projects. The computing infrastructure at TCAG is managed by the SickKids Centre for Computational Biology (CCB) and forms a flexible and capable high performance back end to the centre's 'wet-lab' activities. The TCAG group has supported numerous publications in the leading scientific journals such as Science, Nature, Nature Genetics, PNAS and PLoS, among others.



