1000 Genomes Project publishes analysis of completed pilot phase
Produces tool for research into genetic contributors to human disease
Small genetic differences between individuals help explain why some people have a higher risk than others for developing illnesses such as diabetes or cancer. Today in the journal Nature, the 1000 Genomes Project, an international public-private consortium, published the most comprehensive map of these genetic differences, called variations, estimated to contain approximately 95 per cent of the genetic variation of any person on Earth.
Researchers produced the map using next-generation DNA sequencing technologies to systematically characterise human genetic variation in 180 people in three pilot studies. Moreover, the full scale-up from the pilots is already under way, with data already collected from more than 1,000 people.
“The pilot studies of the 1000 Genomes Project laid a critical foundation for studying human genetic variation. These proof-of-principle studies are enabling consortium scientists to create a comprehensive, publically available map of genetic variation that will ultimately collect sequence from 2,500 people from multiple populations worldwide and underpin future genetics research.”
Richard Durbin PhD, of the Wellcome Trust Sanger Institute and co-Chair of the consortium
Genetic variation between people refers to differences in the order of the chemical units – called bases – that make up DNA in the human genome. These differences can be as small as a single base being replaced by a different one – which is called a single nucleotide polymorphism (abbreviated SNP) – or as large as whole sections of a chromosome being duplicated or relocated to another place in the genome. Some of these variations are common in the population and some are rare. By comparing many individuals to one another and by comparing one population to other populations, researchers can create a map of all types of genetic variation.
The 1000 Genomes Project’s aim is to provide a comprehensive public resource that supports researchers aiming to study all types of genetic variation that might cause human disease. The project’s approach goes beyond previous efforts in capturing and integrating data on all types of variation, and by studying samples from numerous human populations with informed consent allowing free data release without restriction on use. Already, these data have been used in studies of the genetic basis for disease.
“By making data from the project freely available to the research community, it is already impacting research for both rare and common diseases. Biotech companies have developed genotyping products to test common variants from the project for a role in disease. Every published study using next-generation sequencing to find rare disease mutations, and those in cancer, used project data to filter out variants that might obscure their results.”
David Altshuler MD, PhD, Deputy Director of the Broad Institute of Harvard and MIT, and a co-chair of the project
The project has studied populations with European, West African and East Asian ancestry. Using the newest technologies for sequencing DNA, the project’s nine centres sequenced the whole genome of 179 people and the protein-coding genes of 697 people. Each region was sequenced several times, so that more than 4.5 terabases (4.5 million million base letters) of DNA sequence were collected. A consortium involving academic centres on multiple continents and technology companies that developed and sell the sequencing equipment carried out the work.
To process these data required many technical and computational innovations, including standardised ways to organise, store, analyse and share DNA sequencing data. Launched in 2008, the 1000 Genomes Project started with three pilot projects to develop, evaluate and compare strategies for producing a catalogue of genetic variations. Funded through numerous mechanisms by foundations and national governments, the 1000 Genome Project will cost some $120 million over five years, ending in 2012.
When the work began, sequencing was very expensive, so the project began with two approaches aimed at increasing efficiency: One strategy, called ‘low-pass’, combines partial data from many people; the second, only focused on the part of the genome that encodes protein-coding genes. By comparing these strategies to ‘gold standard’ data produced at great completeness and accuracy, the project was able to show that both the alternative approaches work well and have complementary strengths. Researchers will use both strategies in the full-scale project because, although sequencing costs have decreased, it is still relatively expensive.
“We have shown for the first time that a new approach to sequencing – low coverage of many samples – works efficiently and well. This proof-of-principle is now being applied not only in the 1000 Genomes Project, but in disease research, as well.”
Gil McVean PhD, Professor of Statistical Genetics at the University of Oxford
The resulting map of human genetic variation includes about 15 million SNPs, 1 million short insertion/deletion changes, and more than 20,000 structural variations. Many of the genetic variants had previously been identified, but more than half were new. The project’s database contains more than 95 per cent of the currently measurable variants found in any individual, and continuing work will eventually identify more than 99 per cent of human variants.
“What really excites me about this project is the focus on identifying variants in the protein-coding genes that have functional consequences. These will be extremely useful for studies of disease and evolution.”
Richard Gibbs PhD, Director of the Human Genome Sequencing Center at the Baylor College of Medicine (one of the project’s sequencing centres)
The improved map produced some surprises. For example, the researchers discovered that on average, each person carries between 250 and 300 genetic changes that would cause a gene to stop working normally, and that each person also carried between 50 and 100 genetic variations that had previously been associated with an inherited disease. No human carries a perfect set of genes. Fortunately, because each person carries at least two copies of every gene, individuals likely remain healthy, even while carrying these defective genes, if the second copy works normally.
In addition to looking at variants that are shared between many people, the researchers also investigated in detail the genomes of six people: two mother-father-daughter nuclear families. By finding new variants present in the daughter but not the parents, the team was able to observe the precise rate of mutations in humans, showing that each person has approximately 60 new mutations that are not in either parent.
With the completion of the pilot phase, the 1000 Genomes Project has moved into full-scale studies in which 2,500 samples from 27 populations will be studied over the next two years. Data from the pilot studies and the full-scale project are freely available on the project website: www.1000genomes.org.
Researchers studying specific illnesses, such as heart disease or cancer, use maps of genetic variation to help them identify genetic changes that may contribute to the illnesses. Over the last five years, the first generation of such studies (called genome-wide association studies or GWAS) have been based on an earlier map of genetic variation called the HapMap. Built using older technology, HapMap lacks the completeness and detail of the 1000 Genomes Project.
“The 1000 Genomes Project map fills in the gaps between the HapMap landmarks, helping researchers identify all candidate genes in a region associated with a disease. Once a disease-associated region of the genome is identified, experimental studies must be done to identify which variants, genes, and regulatory elements cause the increased disease risk. With the new map, researchers can just look up all the candidate genes and almost all of the variants in the database, saving them many steps in finding the causes.”
Lisa Brooks PhD, Program Director for genetic variation at the National Human Genome Research Institute, a part of the National Institutes of Health
A full list of funding agencies is available at the Nature website.
Organizations that committed major support to the project include: 454 Life Sciences, a Roche company, Branford, Conn.; Life Technologies Corporation, Carlsbad, Calif.; BGI-Shenzhen, Shenzhen, China; Illumina Inc., San Diego; the Max Planck Institute for Molecular Genetics, Berlin, Germany; the Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK; and the National Human Genome Research Institute, which supports the work being done by Baylor College of Medicine, Houston, Texas; the Broad Institute, Cambridge, Mass.; and Washington University, St. Louis, Missouri. Researchers at many other institutions are also participating in the project including groups in Barbados, Canada, China, Colombia, Finland, the Gambia, India, Malawi, Pakistan, Peru, Puerto Rico, Spain, the UK, the US, and Vietnam.
Additional information about the project, including a list of all participants and organizations, can be found at http://www.1000genomes.org/
The National Human Genome Research Institute is one of 27 institutes and centers at National Institutes of Health, an agency of the Department of Health and Human Services. NHGRI’s Division of Extramural Research supports grants for research and for training and career development.
The European Molecular Biology Laboratory is a basic research institute funded by public research monies from 20 member countries and supports research by approximately 85 independent groups covering the spectrum of molecular biology.
European Bioinformatics Institute (EBI) is part of the European Molecular Biology Laboratory (EMBL) and is located on the Wellcome Trust Genome Campus in Hinxton near Cambridge (UK).
The Eli and Edythe L. Broad Institute of MIT and Harvard, founded in 2003 by MIT, Harvard and its affiliated hospitals, and Los Angeles philanthropists Eli and Edythe L. Broad, includes faculty, professional staff and students from throughout the MIT and Harvard biomedical research communities and beyond, with collaborations spanning over a hundred private and public institutions in more than 40 countries worldwide.
The Wellcome Trust Sanger Institute, which receives the majority of its funding from the Wellcome Trust, was founded in 1992. The Institute is responsible for the completion of the sequence of approximately one-third of the human genome as well as genomes of model organisms and more than 90 pathogen genomes. In October 2006, new funding was awarded by the Wellcome Trust to exploit the wealth of genome data now available to answer important questions about health and disease.
The Wellcome Trust is a global charitable foundation dedicated to achieving extraordinary improvements in human and animal health. We support the brightest minds in biomedical research and the medical humanities. Our breadth of support includes public engagement, education and the application of research to improve health. We are independent of both political and commercial interests.
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