Wellcome Sanger Institute
The Wellcome Sanger Institute, previously known as The Sanger Centre and Wellcome Trust Sanger Institute, is a non-profit British genomics and genetics research institute, primarily funded by the Wellcome Trust.
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It is located on the Wellcome Genome Campus by the village of Hinxton, outside Cambridge. It shares this location with the European Bioinformatics Institute. It was established in 1992 and 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 five main areas of research: Cancer, Ageing and Somatic Mutation; Cellular Genetics; Human Genetics; Parasite and Microbes; and the Tree of Life.
Facilities and resourcesEdit
In 1993 the then 17 Sanger Centre staff moved into temporary laboratory space at Hinxton Hall in Cambridgeshire. This 55-acre (220,000 m2) site was to become the Wellcome 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. In discussing the name of the centre, Sanger (still alive when the centre was opened) told John Sulston, the founding director, that the centre "had better be good." Sulston commented, "I rather wished I hadn’t asked."
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.
This section needs to be updated.April 2015)(
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
- Mouse Genetics Project, including a database of standardised phenotypic analysis for many hundreds of mutant mice.
- Vega, a vertebrate genome annotation resource
Several databases were initiated at the Sanger Institute but are now hosted elsewhere:
- MEROPS, a peptidase database
- Pfam, a protein family database
- Rfam, an RNA family database
- TreeFam, a database of phylogenetic trees for animal genes
- WormBase, a database on the biology and sequence of the model organism C. elegans and other related Nematodes.
- WormBase ParaSite, a database for the genomics for parasitic helminths (both Nematodes and Platyhelminthes).
Scientific research at the Sanger Institute is organised into five Scientific Programmes, each defining a major area of research with a particular biological, disease or analytic focus. The current Programmes at the Sanger Institute are Cancer, Ageing and Somatic Mutation, Cellular Genetics, Human Genetics, Parasites and Microbes and Tree of Life. Studies from all programmes provide insights into human, pathogen, cellular evolution, the phenotypic and hence biological consequences of genome variation and the processes which cause mutations.
Cancer, Ageing and Somatic Mutation ProgrammeEdit
Provides leadership in data aggregation and informatics innovation, develops high-throughput cellular models of cancer for genome-wide functional screens and drug testing, and explores somatic mutation's role in clonal evolution, ageing and development. This Programme includes the Cancer Genome Project.
Cellular Genetics ProgrammeEdit
Explores human gene function by studying the impact of genome variation on cell biology. Large-scale systematic screens are used to discover the impact of naturally occurring and engineered genome mutations in human induced pluripotent cells (hIPSCs), their differentiated derivatives and other cell types. It is one of the founder programmes driving the creation and organisation of the international Human Cell Atlas initiative.
Human Genetics ProgrammeEdit
The 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.
The Programme applies genomics to population-scale studies to identify the causal variants and pathways involved in human disease and their effects on cell biology. It also models developmental disorders to explore which physical aspects might be reversible.
Pathogens and Microbes ProgrammeEdit
Investigates the common underpinning mechanisms of evolution, infection and resistance to therapy into bolster understanding of bacteria, viruses and parasites, with a particular interest in malaria. It also explores the effects of genome variation on the biology of host-pathogen interactions, in particular host response to infection and the role of microiotia in health and disease. All the genomes after sequencing are made available at the web-based onsite-maintained database, GeneDB.
Tree of Life ProgrammeEdit
The Tree of Life Programme was created in 2019 to investigate the diversity of complex organisms found in the UK through sequencing and cellular technologies. It also compares and contrasts species' genome sequences to unlock insights into evolution and conservation. This Programme will play a leading role in the Darwin Tree of Life Project, a UK-wide initiative to sequence the genomes of all 66,000 complex species (eukaryotes) in the British Isles.
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:
- 1000 Genomes Project
- GENCODE and ENCODE (ENCyclopedia Of DNA Elements)
- International Cancer Genome Consortium
- International HapMap Project
- International Knockout Mouse Consortium
- International Mouse Phenotyping Consortium
- SNP (Single nucleotide polymorphism) Consortium
- The Copy Number Variation Project
- The genome sequencing of S. pombe, C. elegans, mouse and the Malaria parasite.
- The Human Genome Project
- The UK 10,000 Genomes Project (UK10K)
- 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.
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.
The Institute operates two PhD training programmes: a four-year course for basic science graduates, and a three-year course for clinicians. The four-year course requires 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 and one informatics-based rotation project. Institute houses approximately 50 pre-doctoral students, all of whom are registered at the University of Cambridge.
According to Companies House the five officers of the parent company Genome Research Limited are Henry Parkinson, Kay Elizabeth Davies, Rolf Dieter Heuer, James Cuthbert Smith, David Lindsay Willetts. According to the Sanger website Henry Parkinson is head of legal.
As of 2019[update] a faculty of 32 scientists lead hypothesis-driven research, seeking answers to biomedical questions. Among others, these include Dominic Kwiatkowski, Nicole Soranzo, Michael Stratton and Sarah Teichmann. The institute also has a number of Associate Faculty members, International Fellows and Honorary Faculty. These include Adrian Bird, Ewan Birney, Chris Ponting, Fiona Powrie, Stephen O'Rahilly and Wolf Reik, among others.
Scientific Advisory BoardEdit
The Sanger Board of Management are guided by the scientific advisory board whose members include Professor David Altshuler, Professor Anton Berns, Professor David J. Lipman, Professor Kevin Marsh and Professor Sir Paul Nurse.
Previous faculty members at the Sanger include:
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 US, 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.
In August 2018 it was reported that an investigation was under way into allegations of bullying of staff and gender discrimination made against senior management of the Wellcome Trust Sanger Institute, including the director. The independent investigation, carried out by the barrister Thomas Kibling from Matrix Chambers, concluded in October 2018 and cleared Stratton of any wrongdoing, while listing areas for improvement in the workings of the Sanger Institute.
Human Genome ProjectEdit
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.
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