Centre for Applied Genomics
The Centre for Applied Genomics is a genome centre in the Research Institute of The Hospital for Sick Children, and is affiliated with the University of Toronto. TCAG also operates as a Science and Technology Innovation Centre of Genome Canada,[1] with an emphasis on next-generation sequencing (NGS) and bioinformatics support. Research at TCAG focuses on the genetic and genomic basis of human variability, health and disease, including research on the genetics of autism spectrum disorder and structural variation of the human genome. The centre is located in the Peter Gilgan Centre for Research and Learning in downtown Toronto, Canada.
| Company type | Genome Centre |
|---|---|
| Founded | 1998 |
| Headquarters | , Canada |
Area served | Biomedical research |
Key people | Stephen W. Scherer, scientific director |
| Services | Experimentation, project consultation, data analysis, bioinformatics |
Number of employees | 70 |
| Parent | The Hospital for Sick Children |
| Website | http://www.tcag.ca/ |
History edit
The need for a centralized core facility for human genome research at SickKids Hospital prompted the establishment of The Centre for Applied Genomics (TCAG) in 1998.[citation needed] The founding director and associate director were Drs. Lap-Chee Tsui and Stephen W. Scherer, respectively. Scherer is now the scientific director.
Funding from the Canada Foundation for Innovation (CFI) enabled TCAG to form by consolidating existing core facilities including the Medical Research Council of Canada Genome Resource Facility, the (CGDN) large insert clone core, the CGDN DNA Sequencing Core and the SickKids Biotechnology Service DNA Sequencing and Synthesis labs. A genome-wide microsatellite genotyping laboratory at the Ottawa Health Research Institute, led by Dennis Bulman, was added. Subsequently, operational funding from the CIHR Genomics Special Projects panel provided for additional staff.
In 2001, a proposal entitled "Genome Resource Core Platform" was submitted to the then newly formed Genome Canada. This provided operational support, enhancing existing facilities and adding a mouse genotyping core at the University of Toronto led by Lucy Osborne.[citation needed] In 2002, SickKids built a new Affymetrix microarray facility. This core has quickly grown to become the largest such service centre in Canada and is in the top ten in North America.[2]
In 2004, TCAG entered a second phase of development driven by a $12 million CFI/ funded project entitled "Integrative Genomics for Health Research",[3] allowing for consolidation of the mouse genotyping core with the SickKids facilities. This award also supported the establishment of an "Ontario Population Genomics Repository" (OPGP) to be used as controls in studies of common diseases. To efficiently complete this project, TCAG partnered with John McLaughlin's group at Mount Sinai Hospital (Toronto).
In May, 2004, an application to the newly announced CFI Research Hospital Fund resulted in a $10.9 million award to build out lab space and consolidate all operations on the 14th and 15th floors of the Toronto Medical Discovery Tower (TMDT) in the MaRS Discovery District. TCAG was the first occupant of TMDT (in August, 2005), quickly followed by other SickKids scientists. Investments in computer infrastructure from the 2003 CFI/ competition resulted in the establishment of new phases of the (HPF) that is currently used by TCAG and many other users, to allow analysis of large genomic datasets arising from new microarray and sequencing technologies. Further enhancements to the TCAG infrastructure were supported by a $10.7 million renewal grant from CFI's Leading Edge Fund competition, entitled "Integrative Genomics for Health Research – Phase II", awarded in June 2009.[4] More recently, a CFI grant entitled "The Centre for Applied Genomics: Paediatric Genomes to Outcomes" provided further infrastructure support.[5] In October 2013, TCAG moved to the Peter Gilgan Centre for Research and Learning, a new building housing the SickKids Research Institute.[6]
TCAG operates in large part on Science and Technology Innovation Centre (STIC) funds from Genome Canada, administered by the Ontario Genomics Institute.
Research edit
Current research at TCAG centres around large-scale projects performed by facility personnel, including support of Genome Canada projects, and a significant focus on the genetics of autism spectrum disorders and structural variation of the human genome. Service work is also performed for over 600 other academic, private sector and government labs each year, drawn from 30 different countries and spanning a wide variety of research disciplines.[7]
Past research at TCAG is reflected by numerous peer-reviewed scientific publications. In 2008, TCAG Scientific Directors, Associate Scientists and staff co-authored 58 peer-reviewed manuscripts dependent in some way (either entirely, or in part) on the platform infrastructure, as documented in PubMed.[8] Since 2002, over 270 such papers have been published.[9] Support of other researchers worldwide is found in many similar publications, with at least 145 papers in scholarly journals, book chapters, or graduate thesis dissertations acknowledging support or use of database resources during 2008 alone.[10]
Historical papers include:
- Discovery of genes involved in predisposition to medulloblastoma (Michael Taylor and James Rutka with TCAG support)[11]
- Gene identification in Shwachman-Diamond syndrome (with Johanna Rommens and others)[12]
- Gene identification in Lafora Epilepsy (with Berge Minassian)[13] and its canine counterpart[14]
- A disease-relevant MECP2 isoform involved in Rett syndrome[15]
- Involvement of the SUMO4 gene in type I diabetes[16]
- Severe expressive-language delay related to duplication of the Williams–Beuren locus[17]
TCAG was also integral to publications describing the decoding of human chromosome 7,[18] the discovery of large-scale copy number variation in the human genome,[19][20] and the analysis of the first diploid human genome sequence (with the J. Craig Venter Institute).[21]
Genome Canada projects edit
As a Science and Technology Innovation Centre of Genome Canada, TCAG currently supports numerous large-scale projects, including research on autism spectrum disorders, structural variation of the human genome, integrative biology, conditional mouse mutagenesis, interactions of signaling molecules, type I diabetes, cancer stem cells, Cystic Fibrosis, biodiversity, structural biology, and stem cells, from Genome Canada's Competition III, New Technology Development and Applied Genomics Research in Bioproducts or Crops (ABC) competitions.[22][23][24] The centre is now working with applicants in the Large-Scale Applied Research Project[25] and Advancing Technology Innovation Through Discovery[26] competitions.
Databases edit
TCAG also hosts and curates websites and databases developed from supported projects, namely The Chromosome 7 Database, The Database of Genomic Variants,[27] the Segmental Duplication Database, the Autism Chromosome Rearrangement Database, and others.[28] These databases contain publicly available information.
Core facilities edit
TCAG employs a variety of genomic technologies to support different types of experimentation. These are organized into separate Core Facilities, with dedicated managers.
Informatics and biostatistics edit
The Bioinformatics team assists with data handling and analysis, and develops new algorithms and analytical methods, with a focus on the analysis of high-throughput ("next-generation") sequencing data. The Statistical Analysis group provides project consultation and power analysis, statistical analysis (genetic, microarray, and pathway data, epidemiology, population genetics), and copy number variation analysis, as well as developing new statistical methods.
DNA sequencing and synthesis edit
The facility uses conventional capillary Sanger sequencing on Applied Biosystems 3730xl instruments, governed by a Laboratory Information Management System (LIMS). Additionally, next-generation sequencing (NGS) using Illumina HiSeq 2500 and HiScan SQ instruments, Life Technologies Ion Proton and Applied Biosystems SOLiD instruments, and a 454/Roche GS-FLX Titanium instrument is performed. A key component of this facility is the use of high-performance computing and bioinformatics support for NGS analysis.
The Oligonucleotide Synthesis component of this facility makes conventional, long (up to 120 bases) and modified oligonucleotides, and purifies these by desalting, cartridge or high-performance liquid chromatography (HPLC).
Microarray and genetic analysis edit
The Microarray and Gene Expression Core Facility has a dedicated manager, and operates technologies from Affymetrix, Agilent and Illumina. Additionally, there is a wide variety of analytical software packages available for on-site data analysis.
Cytogenomics and genome resources edit
The Cytogenomics and Genome Resources Core Facility has a single manager between these two functions. Cytogenomics includes karyotyping and spectral (SKY) karyotyping (for mouse, human, and other species), fluorescent in situ hybridization (FISH) mapping, transgenic insertion site mapping (G-to-FISH mapping) and clone labeling for FISH experiments. The Genome Resources components includes a clone repository (Mammalian Gene Collection (MGC) cDNA (mouse and human), genomic clones including human bacterial artificial chromosomes (BACs)) and provides project consultation and design assistance (annotation, database queries, probe selection). It also provides cDNA library screening and quantitative PCR.
Genetic analysis edit
The Genetic Analysis area includes capillary-based genotyping (Applied Biosystems TaqMan and SNaPshot, microsatellites), custom genotyping (e.g. heteroduplex analysis), mouse genotyping (for cross progeny and genetic linkage analysis), and methylation analysis (for epigenetics research).
Biobanking edit
The Biobanking Core Facility has its own dedicated manager. It performs white cell immortalization (from blood) and banking, fibroblast culture and banking, culture and banking of other cell types including non-human cells, genomic DNA preparation from blood, saliva, tissues or cells, and whole-genome amplification (WGA).
Funding sources edit
TCAG is funded by several agencies, including the Canada Foundation for Innovation (CFI), Genome Canada through the Ontario Genomics Institute, the Ontario Ministry of Research and Innovation. Additionally, philanthropic donations are administered by The Hospital for Sick Children Foundation, and specific research projects are funded by a wide variety of agencies and charitable foundations.
Organization and management edit
Scientific director edit
The scientific director of TCAG is Stephen W. Scherer, senior staff scientist in The Hospital for Sick Children's Research Institute, director of the McLaughlin Centre,[29] and a professor at the University of Toronto.[30]
Scientific management committee edit
TCAG is governed by a scientific management committee, who meet regularly to discuss high-level strategic planning. The scientific management committee consists of:
- Gary Bader
- Michael Brudno
- Christian Marshall
- Andrew Paterson
- Adam Shlien
- Lisa Strug
- Martin Somerville
- Michael Wilson
- Ryan Yuen
Bader and Brudno are located at the University of Toronto, and the others at The Hospital for Sick Children. The committee also includes three ex officio members: the assistant director, facility manager, and a representative from the Ontario Genomics Institute.
Associate investigators edit
Since 2006, TCAG has appointed associate investigators. These associates consult on their specific areas of expertise, and assist in identification and implementation of new technologies. At present, there are nineteen associate investigators: Drs. Moumita Barua (U of Toronto), Jonathan Beauchamp (U of Toronto), Sarah Bowdin (Ted Rogers Centre for Heart Research), Jennifer Brooks (U of Toronto), Brendan Frey (U of Toronto), Ann George (SickKids), Zhenya Ivakine (SickKids), Pingzhao Hu (U of Manitoba), Melanie Mahtani (Prime Genomics), Daniele Merico (Deep Genomics), Esteban Parra (UTM), Mary Shago (SickKids), Mark Silverberg (MSH), James Stavropoulos (SickKids), Michael Taylor (SickKids), Mohammad Uddin (Mohammad Bin Rashid University), John Vincent (CAMH), Suzi Walker (Genomics England), and Marc Woodbury-Smith (Newcastle University).
Scientific advisory board edit
High-level scientific oversight of TCAG's scientific mandate and operations is provided through an external scientific advisory board (SAB). The SAB members are:
- Edward M. Rubin (Chair), Metabiota
- Mark Blaxter, Tree of Life Programme, Wellcome Sanger Institute
- Elaine Mardis, Institute for Genomic Medicine, Nationwide Children's Hospital
- Gabor Marth, University of Utah
- Roderick McInnes, Lady Davis Research Institute, Jewish General Hospital
- Richard Myers, HudsonAlpha Institute for Biotechnology
The Ontario Genomics Institute (OGI) and Genome Canada also provide ex officio members.
References edit
- ^ . Archived from the original on 2008-10-19. Retrieved 2008-06-20.
- ^ Data provided by Affymetrix, Inc.
- ^ Integrative Genomics for Health Research news item (Ontario Innovation Trust website) [1] 2011-07-06 at the Wayback Machine
- ^ SickKids press release, June 18, 2009
- ^ SickKids kicks off 2013 with two Leading Edge Fund grants, January 13, 2013
- ^ The Centre for Applied Genomics has moved - news item, TCAG website, October 229, 2013
- ^ Data from progress reports submitted to the Ontario Genomics Institute
- ^ PubMed search for publications authored by these individuals during calendar year 2008, excluding Brudno, who was added in 2009 [2][citation needed]
- ^ PubMed search for publications authored by these individuals, 2002 through present, excluding Drs. Brudno and Beyene who were added more recently [3][citation needed]
- ^ Google Scholar full-text search results: publications referring to The Centre for Applied Genomics or the Database of Genomic Variants, either in the Acknowledgments section or body text, and published either electronically or in print. Strategies used were: "TCAG" (ignoring hits from other TCAG acronyms and various DNA sequences), "The Centre for Applied Genomics", American spelling, "The Center for Applied Genomics" (ignoring hits from facilities with similar names), "DGV", "Database of Genomic Variants", "Data Base of Genomic Variants" (including hits from the hyphenated form, "Data-base"), "Toronto Database" (ignoring non-relevant hits from non-DGV databases).
- ^ Taylor MD, Liu L, Raffel C, et al. (July 2002). "Mutations in SUFU predispose to medulloblastoma". Nature Genetics. 31 (3): 306–10. doi:10.1038/ng916. PMID 12068298. S2CID 6882566.
- ^ Boocock GR, Morrison JA, Popovic M, et al. (January 2003). "Mutations in SBDS are associated with Shwachman-Diamond syndrome". Nature Genetics. 33 (1): 97–101. doi:10.1038/ng1062. PMID 12496757. S2CID 5091627.
- ^ Chan EM, Young EJ, Ianzano L, et al. (October 2003). "Mutations in NHLRC1 cause progressive myoclonus epilepsy". Nature Genetics. 35 (2): 125–7. doi:10.1038/ng1238. PMID 12958597. S2CID 32590557.
- ^ Lohi H, Young EJ, Fitzmaurice SN, et al. (January 2005). "Expanded repeat in canine epilepsy". Science. 307 (5706): 81. doi:10.1126/science.1102832. PMID 15637270. S2CID 39280939.
- ^ Mnatzakanian GN, Lohi H, Munteanu I, et al. (April 2004). "A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome". Nature Genetics. 36 (4): 339–41. doi:10.1038/ng1327. PMID 15034579.
- ^ Qu H, Bharaj B, Liu XQ, et al. (February 2005). "Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes". Nature Genetics. 37 (2): 111–2, author reply 112–3. doi:10.1038/ng0205-111. PMID 15678135.
- ^ Somerville MJ, Mervis CB, Young EJ, et al. (October 2005). "Severe expressive-language delay related to duplication of the Williams-Beuren locus". The New England Journal of Medicine. 353 (16): 1694–701. doi:10.1056/NEJMoa051962. PMC 2893213. PMID 16236740.
- ^ Scherer SW, Cheung J, MacDonald JR, et al. (May 2003). "Human chromosome 7: DNA sequence and biology". Science. 300 (5620): 767–72. Bibcode:2003Sci...300..767S. doi:10.1126/science.1083423. PMC 2882961. PMID 12690205.
- ^ Iafrate AJ, Feuk L, Rivera MN, et al. (September 2004). "Detection of large-scale variation in the human genome". Nature Genetics. 36 (9): 949–51. doi:10.1038/ng1416. PMID 15286789.
- ^ Redon R, Ishikawa S, Fitch KR, et al. (November 2006). "Global variation in copy number in the human genome". Nature. 444 (7118): 444–54. Bibcode:2006Natur.444..444R. doi:10.1038/nature05329. PMC 2669898. PMID 17122850.
- ^ Levy S, Sutton G, Ng PC, et al. (September 2007). "The diploid genome sequence of an individual human". PLOS Biology. 5 (10): e254. doi:10.1371/journal.pbio.0050254. PMC 1964779. PMID 17803354.
- ^ . Archived from the original on 2008-10-19. Retrieved 2008-06-20.
- ^ Summary of New Technology Development projects on the Genome Canada website.[4] 2009-05-23 at the Wayback Machine
- ^ Competition in Applied Genomics Research in Bioproducts or Crops (ABC) – Genome Canada website. [5] 2008-10-19 at the Wayback Machine
- ^ Large-Scale Applied Research Project Competition, Genome Canada website. [6] 2010-11-24 at the Wayback Machine
- ^ Advancing Technology Innovation Through Discovery Competition, Genome Canada website.[7] 2010-11-13 at the Wayback Machine
- ^ Database of Genomic Variants
- ^ . Archived from the original on 2008-05-08. Retrieved 2008-06-20.
- ^ . Archived from the original on 2009-02-05. Retrieved 2010-03-08.
- ^ Steve Scherer biographical web page
External links edit
- TCAG website at www.tcag.ca
- Database of Genomic Variants