|Wellcome Trust Sanger Institute|
|Location||Hinxton, Cambridgeshire, United Kingdom|
|Address||Wellcome Trust Genome Campus|
It is located on the Wellcome Trust Genome Campus by the village of Hinxton, outside Cambridge. It shares this location with the European Bioinformatics Institute. It was established in 1992 as The Sanger Centre, named after double Nobel Laureate, Frederick Sanger. It was conceived as a large scale DNA sequencing centre to participate in the Human Genome Project, and went on to make the largest single contribution to the gold standard sequence of the human genome. From its inception the Institute established and has maintained a policy of data sharing, and does much of its research in collaboration.
Since 2000, the Institute expanded its mission to understand "the role of genetics in health and disease". The Institute now employs around 900 people and engages in four main areas of research: Human genetics, pathogen genetics, mouse and zebrafish genetics and bioinformatics.
The Wellcome Trust Sanger Institute was established in 1992, funded by the Wellcome Trust and the UK's Medical Research Council. One of the primary goals of the Institute on its creation, was to "play a role in mapping, sequencing and decoding the human genome and the genomes of other organisms". The Sanger Institute now hosts several research programmes aiming to elucidate the associations between genes and biological traits - most often disease susceptibilities. The Sanger Institute has, since inception, maintained a policy that "aims to provide rapid access to data sets of use to the research community".
In 1993 the then 17 Sanger Institute staff moved into temporary laboratory space at Hinxton Hall in Cambridgeshire. This 55-acre (220,000 m2) site was to become the Wellcome Trust Genome Campus, which has a growing population of around 1300 staff, approximately 900 of whom work at the Sanger Institute. The Genome Campus also includes the Wellcome Trust Conference Centre  and the European Bioinformatics Institute. A major extension of the campus was officially opened in 2005; the buildings accommodate new laboratories, a data centre and staff amenities.
Human Genome Project
The Sanger Institute was opened in 1993, three years after the inception of the Human Genome Project, and went on to make the largest single contribution to the gold standard sequence of the human genome, published in 2004. The Institute was engaged in collaborations to sequence 8 of the 23 human pairs of chromosomes (1, 6, 9, 10, 13, 20, 22, and X). Since the publishing of the human genome, research carried out at the Institute has developed beyond sequencing of organisms into various biomedical research areas, including studies into diseases such as cancer, malaria and diabetes.
John E. Sulston was the founding Director of the Sanger Institute. Sulston was instrumental in the choice of the Hinxton site for the Institute and remained there as Director until the announcement of the completion of the draft human genome in 2000. Sulston graduated from the University of Cambridge in 1963 and completed his PhD on the chemical synthesis of DNA in 1966. He shared the 2002 Nobel Prize in Physiology or Medicine with Robert Horvitz and Sydney Brenner, two years after standing down as Director of the Institute.
In 2000, Allan Bradley left his appointment as Professor at the Baylor College of Medicine, in the USA, to take up the position as Director of the Sanger Institute. Bradley wanted to build on the achievements made by the Sanger Institute in the Human Genome Project by "concentrating on gene function, cancer genomics, and the genomes of model organisms such as the mouse and the zebrafish". Bradley received his BA, MA and PhD in Genetics from the University of Cambridge.
In 2010, Bradley stepped down from his leadership role to form a startup company, but remains on the faculty of the Institute as Director Emeritus. Mike Stratton, who is a leader of the Cancer Genome Project and the International Cancer Genome Consortium, was appointed Director of the Sanger Institute in May of that year. 
Since 2000, the Sanger Institute has built on its sequencing skills to develop new programmes in postgenomic biology - understanding the messages in genes. The Institute engages in four main areas of research:
The hall Institute's research in human genetics focuses on the characterisation of human genetic variation in health and disease. Aside from the Institute's contribution to the Human Genome Project, researchers at the Sanger Institute have made contributions in various research areas relating to disease, population comparative and evolutionary genetics. In January 2008, the launch of the 1000 Genomes Project, a collaboration with scientists around the globe, signalled an effort to sequence the genomes of 1000 individuals in order to create the "most detailed map of human genetic variation to support disease studies". The data from the pilot projects was made freely available in public databases in June 2010. In 2010, the Sanger Institute announced its participation in the UK10K project, which will sequence the genomes of 10,000 individuals to identify rare genetic variants and their effects on human health. The Sanger Institute is also part of the International Cancer Genome Consortium, an international effort to describe different cancer tumour types. It is also part of the GENCODE and ENCODE research programmes to create an encyclopaedia of DNA elements.
Mouse and zebrafish genetics programme at the Sanger Institute uses genome sequence of these model organisms to understand basic biological mechanisms, and gene function in human health and disease. Projects include the study of development, cancer, hearing and behaviour.
The Institute carries out research in pathogen genetics to bolster understanding of the effects of genome variation on the biology of host-pathogen interactions. Research is underway at the Sanger Institute into the genomes of pathogens including many bacteria, viruses and parasites. The Pathogen Sequencing Advisory Group (PSAG) considers proposals or suggestions for sequencing of any genome of particular importance. All the genomes after sequencing are made available at the web-based onsite-maintained database, GeneDB.
The Sanger Institute's bioinformatics teams have developed IT systems for sequencing and postgenomic research. The Institute houses genome resources, RNA, protein and other family resources and functional annotation databases and resources. Researchers worldwide are able to use these resources to make inferences of genomic knowledge through computational analysis and integration of data.
The Sanger Institute's Sequencing staff handle millions of DNA samples each week. The Institute "capitalises on leading-edge technologies to answer questions unanswerable only a few years ago". The advances in technology allow the Sanger Institute to carry out sequencing of the genomes of individual humans, vertebrate species and pathogens, at an ever increasing pace and reducing cost. The Institute has more than 100 ongoing pathogen sequencing projects. The output of the Sanger Institute is around 10 billion bases of raw sequence data per day.
The Sanger Institute is home to a Faculty of nearly 40 experts whose areas of interest represent the Sanger Institute's genetics research programmes. These research leaders engage in hypothesis-driven science in a variety of scientific fields. They are:
|Adams, David||Experimental Cancer Genetics|
|Anderson, Carl||Statistical Genetics|
|Barrett, Jeffrey||Statistical and computational genetics of human disease|
|Barroso, Inês||Metabolic Disease Group|
|Berriman, Matt||Parasite Genomics|
|Billker, Oliver||Malaria Programme|
|Bradley, Allan||Mouse Genomics|
|Campbell, Peter||Cancer Genome Project|
|Deloukas, Panos||Genetics of complex traits in humans|
|Dougan, Gordon||Microbial Pathogenesis|
|Durbin, Richard||Genome Informatics|
|Gaffney, Daniel||Population and evolutionary genomics of gene regulation|
|Hubbard, Tim||Vertebrate Genome Analysis|
|Hurles, Matthew||Genome Dynamics and Evolution|
|Kellam, Paul||Virus Genomics|
|Kwiatkowski, Dominic||Malaria Programme|
|Lawley, Trevor||Bacterial Pathogenesis|
|Liu, Pentao||Mouse Cancer Genetics|
|Logan, Darren||Genetics of Instinctive Behaviour|
|McDermott, Ultan||Cancer Genome Project|
|Mustonen, Ville||Population Genomics of Molecular Phenotypes|
|Palotie, Aarno||Genetics of Common Neurological Diseases|
|Parkhill, Julian||Pathogen Sequencing|
|Rayner, Julian||Malaria Programme|
|Sandhu, Manj||Genetic Epidemiology|
|Skarnes, Bill||Gene Trap Mutagenesis|
|Soranzo, Nicole||Genomics of quantitative trait variation in humans|
|Stemple, Derek||Vertebrate Development and Genetics|
|Stratton, Mike||Cancer Genome Project|
|Tyler-Smith, Chris||Human Evolution|
|Wright, Gavin||Cell Surface Signalling Laboratory|
|Yadav, Vijay||Systems biology of Bone|
|Zeggini, Eleftheria||Applied Statistical Genetics|
Much of the Sanger Institute's research is carried out in partnership with the wider scientific community; over 90 percent of the Institute's research papers involve collaborations with other organisations. Significant collaborations include:
- The Human Genome Project
- SNP (Single nucleotide polymorphism) Consortium
- International HapMap Project
- The genome sequencing of S. pombe, C. elegans, mouse and the Malaria parasite.
- The Wellcome Trust Case Control Consortium 
- The Copy Number Variation Project 
- International Knockout Mouse Consortium
- 1000 Genomes Project
- International Cancer Genome Consortium
- GENCODE and ENCODE (ENCyclopedia Of DNA Elements)
- The UK 10,000 Genomes Project (UK10K) 
- International Mouse Phenotyping Consortium
- Wellcome Trust - Department of Biotechnology, India Alliance
The Sanger Institute has a programme of public engagement activity. The programme aims to make complex biomedical research accessible to a range of audiences including school students and their teachers, and local community members.
The Communication and Public Engagement programme aims to "encourage informed discussion about issues relevant to Sanger Institute research" and "foster a community of researchers who can engage effectively with different audiences". The Institute hosts visits for more than 1,500 students, teachers and community groups per year. Visitors may meet scientific staff, tour the Institute and its facilities, and participate in ethical debates and activities. The programme also offers professional development sessions for teachers of GCSE and post 16 science through the national network of Science Learning Centres, and by hosting visits for groups interested in updating their knowledge in contemporary genetics. Videoconferencing into the Sanger Institute is also offered for Science Learning Centres, Science Centres and schools.
The programme maintains a dedicated public website, yourgenome.org, that is intended to help people understand genetics and genomics science and its implications for society. The website includes teaching resources for secondary school science teachers that have been developed with Institute researchers.
Scientific and public engagement staff also collaborate on and contribute to national projects such as the UK's InsideDNA  traveling exhibition and the Who am I? gallery at The Science Museum. They also participate in public events such as the Cambridge Science Festival.
Bioinformatic databases resources are one of the outcomes of research programmes that the Sanger Institute is involved in. Those hosted by the Sanger Institute include:
- COSMIC, a catalogue of somatic mutations in cancer
- DECIPHER, a database of chromosomal imbalance and phenotype in humans, using Ensembl resources
- Ensembl, a genome browser co-hosted by the European Bioinformatics Institute.
- GeneDB, a pathogen sequence database
- MEROPS, a peptidase database
- Pfam, a protein family database
- Rfam, an RNA family database
- TreeFam, a database of phylogenetic trees for animal genes
- Vega, a vertebrate genome annotation resource
- WormBase, a database on the biology and sequence of the model organism C. elegans and other related Nematodes.
The Institute operates two PhD training programmes: a four year course for basic science graduates, and a thee year course for clinicians. The four year course permits students to rotate around three different laboratories in order to broaden their scientific horizons before choosing a PhD project. Each student is required to choose at least one experimental one informatics-based rotation project. Institute houses approximately 50 pre-doctoral students, all of whom are registered at the University of Cambridge.
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- Wellcome Trust Conference Centre
- "Wellcome Trust Genome Campus Extension Opened: Visit by Her Royal Highness, The Princess Royal". Wellcome Trust Sanger Institute. Retrieved 2009-01-07.
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- Pennisi E (2003). "Reaching Their Goal Early, Sequencing Labs Celebrate". Science 300 (5618): 409. doi:10.1126/science.300.5618.409. PMID 12702850.
- "International Human Genome Sequencing Consortium Announces "Working Draft" of Human Genome". National Human Genome Research Institute. Retrieved 2008-12-09.
- Sulston J, Ferry G (2002). The Common Thread: A story of Science, Politics, Ethics, and the Human Genome. The Joseph Henry Press. p. 18.
- "The Nobel Prize in Physiology or Medicine 2002". Nobel Prize. Retrieved 2009-01-07.
- "Sanger Institute looks to the future". Genome Biology. Retrieved 2008-12-09.
- "Professor Allan Bradley". Wellcome Trust Sanger Institute. Retrieved 2008-12-09.
- "Professor Mike Stratton appointed new Director". Wellcome Trust Sanger Institute. Retrieved 2010-15-20.
- "1000 Genomes: A Deep Catalog of Human Genetic Variation". 1000 Genomes Project. Retrieved 2008-12-22.
- "1000 Genomes Project releases data from pilot projects on path to providing database for 2,500 human genomes". Wellcome Trust Sanger Institute. Retrieved 2010-06-28.
- "Wellcome Trust launches study of 10,000 human genomes in UK". Wellcome Trust Sanger Institute. Retrieved 2010-06-28.
- "International Cancer Genome Consortium Homepage". International Cancer Genome Consortium. Retrieved 2009-01-23.
- "Wellcome Trust Sanger Institute - ENCODE and GENCODE". Retrieved 2010-06-28.
- "Wellcome Trust Sanger Institute - Sequencing". Wellcome Trust Sanger Institute. Retrieved 2010-06-28.
- "Wellcome Trust Sanger Institute - Pathogen genomics". Wellcome Trust Sanger Institute. Retrieved 2010-06-28.
- Jones, I. "Feature: Highly cited". Wellcome Trust. Retrieved 2009-01-22.
- "Wellcome Trust Sanger Institute - Academic Facult". Wellcome Trust Sanger Institute. Retrieved 2010-06-28.
- Figure based on data for 2008 retrieved from SCOPUS website
- Wellcome Trust Case Control Consortium
- Copy Number Variation Project
- UK10K (the UK 10,000 Genomes Project)
- "Team 104: Communication and Public Engagement Programme". Wellcome Trust Sanger Institute. Retrieved 2009-01-12.
- Who am I? gallery
- COSMIC, a catalogue of somatic mutations in cancer
- GeneDB, a pathogen sequence database
- "Wellcome Trust Sanger Institute PhD Programmes". Wellcome Trust Sanger Institute. Retrieved 2009-11-13.
- The Sanger Institute
- Wellcome Trust Sanger Institute on Twitter
- Your Genome (Sanger Institute run Public Engagement website)
- Hinxton: Courses and Conferences
- Sir John Sulston awarded a share in the 2002 Nobel Prize for Physiology or Medicine
- The Wellcome Trust Case Control Consortium
- Dodson G (2005). "Fred Sanger: sequencing pioneer". The Biochemist 27: 31-35.
- Sanger F, Lagnado J (2005). "Fred Sanger: The Interview". The Biochemist 27: 37-39.
- Sanger, F. (1988). "Sequences, Sequences, and Sequences". Annual Review of Biochemistry 57: 1–29. doi:10.1146/annurev.bi.57.070188.000245. PMID 2460023.
- About Fred Sanger, biography from the Sanger Institute