International Human Genome Sequencing Consortium Announces "Working Draft" of Human Genome

June 2000

The Human Genome Project (HGP) public consortium today announced that it has assembled a working draft of the sequence of the human genome - the genetic blueprint for a human being.

This major milestone involved two tasks: placing large fragments of DNA in the proper order to cover all of the human chromosomes, and determining the DNA sequence of these fragments.

The assembly reported today consists of overlapping fragments covering 97 percent of the human genome, of which sequence has already been assembled for approximately 85 percent of the genome. The sequence has been threaded together into a string of As, Ts, Cs, and Gs arrayed along the length of the human chromosomes.

Production of genome sequence has skyrocketed over the past year, with more than 60 percent of the sequence having been produced in the past six months alone. During this time, the consortium has been producing 1000 bases a second of raw sequence -- 7 days a week, 24 hours a day.

The average quality of the "working draft" sequence far exceeds the consortium's original expectations for this intermediate product. (Note to journalists: HGP fact sheet in press kit contains definitions of working draft, etc.)

Consortium centers have produced far more sequence data than expected (over 22.1 billion bases of raw sequence data, comprising overlapping fragments totaling 3.9 billion bases and providing 7-fold sequence coverage of the human genome).

As a result, the working draft is substantially closer to the ultimate "finished" form than the consortium expected at this stage. Approximately 50 percent of the genome sequence is in near-finished form or better, and 24 percent of it is in completely "finished" form. Across the genome, the average DNA segment resides in a continuous gapless sequence "contig" of 200,000 bases. The average accuracy of all of the DNA sequence in this assembly is 99.9 percent.

The sequence information from the public project has been continuously, immediately and freely released to the world, with no restrictions on its use or redistribution. The information is scanned daily by scientists in academia and industry, as well as by commercial database companies providing information services to biotechnologists.

Already, many tens of thousands of genes have been identified from the genome sequence. Analysis of the current sequence shows 38,000 predicted genes confirmed by experimental evidence. There are many thousands of additional gene predictions to be tested experimentally. Dozens of disease genes have been pinpointed by access to the working draft.

Consortium goals

The consortium's goal for the spring of 2000 was to produce a working draft version of the human sequence, an assembly containing overlapping fragments that cover approximately 90 percent of the genome and that are sequenced in working draft form, i.e., with some gaps and ambiguities. The consortium's ultimate goal is to produce a completely finished sequence, i.e., one with no gaps and 99.99 percent accuracy. The target date for this ultimate goal had been 2003, but today's results mean that the final, stand-the-test-of-time sequence will likely be produced considerably ahead of that schedule.

Complementary approaches

In a related announcement, Celera Genomics announced today that it has completed its own first assembly of the human genome DNA sequence.

The public and private projects use similar automation and sequencing technology, but different approaches to sequencing the human genome. The public project uses a "hierarchical shotgun" approach in which individual large DNA fragments of known position are subjected to shotgun sequencing (i.e., shredded into small fragments that are sequenced, and then reassembled on the basis of sequence overlaps).

The Celera project uses a "whole genome shotgun" approach, in which the entire genome is shredded into small fragments that are sequenced and put back together on the basis of sequence overlaps.

The hierarchical shotgun method has the advantage that the global location of each individual sequence is known with certainty, but it requires constructing a map of large fragments covering the genome. The whole shotgun method does not require this step, but presents other challenges in the assembly phase.

Both approaches align the sequence along the human chromosomes by using landmarks contained in the physical map produced by the HGP.

"The two approaches are quite complementary. The public project and Celera plan to discuss the relative scientific merits of the methods employed by the two projects. In the end, the best approach may well be to use a combination of the methods for sequencing future genomes," said Francis Collins, M.D., Ph.D., director of the National Human Genome Research Institute (NHGRI) of the National Institutes of Health (NIH). In fact, current plans by the public project to sequence the genome of the laboratory mouse involve this hybrid strategy.

Next phase

The HGP will now focus on converting the working draft and near-finished sequences to a finished form. This will be done by filling the gaps in the working draft sequence and by increasing the overall sequence accuracy to 99.99 percent. Although the "working draft" version is useful for most biomedical research, a highly accurate sequence that is as close to perfect as possible is critical for obtaining all the information there is to get from human sequence data. This has already been achieved for chromosomes 21 and 22, as well as for 24 percent of the entire genome.

Human DNA variation

The greater-than-expected sequence production has also yielded a bumper crop of human genetic variations -- called single nucleotide polymorphisms or SNPs. The HGP had set a goal of discovering 100,000 SNPs by 2003. Already, with today's assembled sequences and other data accumulated by The SNP Consortium, scientists have now found more than 300,000 SNPs and will likely have 1 million SNPs by year-end. These SNPs provide a powerful tool for studies of human disease and human history.

Background

Sequencing, which is determining the exact order of DNA's four chemical bases, commonly abbreviated A, T, C and G, has been expedited in the HGP by technological advances in deciphering DNA and the collaborative nature of the effort, which includes about 1,000 scientists worldwide working together effectively.

The Human Genome Sequencing Project aims to determine the sequence of the euchromatic portion of the human genome. The euchromatic portion excludes certain regions consisting of long stretches of highly repetitive DNA that encode little genetic information, and that are not recovered in the vector systems used by the genome project. Such regions account for about 10 percent of the genome, and are said to be heterochromatic. (For example, the center of chromosomes, called centromeres, consists of heterochromatic DNA.)

The International Human Genome Sequencing Consortium includes scientists at 16 institutions in France, Germany, Japan, China, Great Britain and the United States. The five largest centers are located at: Baylor College of Medicine, Houston, Texas; Joint Genome Institute in Walnut Creek, CA; Sanger Centre near Cambridge, England; Washington University School of Medicine, St. Louis; and Whitehead Institute, Cambridge, Massachusetts. Together, these five centers have generated about 82 percent of the sequence. The following list provides more detail about the 16 centers and their individual contributions to the HGP.

The project has been tightly coordinated so that no region of the genome is left unattended to, and duplication is minimized. Participants in the international consortium have all adhered to the project's quality standards and to the daily data release policy. The project is funded by grants from government agencies and public charities in the various countries. These include the NHGRI, he Wellcome Trust in England, and the U.S. Department of Energy (DOE).

The total cost for the working draft is approximately $300 million worldwide, with roughly half ($150 million) being funded by the U.S. NIH. The cost of sequencing the human genome is sometimes reported as $3 billion. However, this figure refers to the original estimate of total funding for the HGP over a 15-year period (1990-2005) for a wide range of scientific activities related to genomics. These include studies of human diseases, experimental organisms (such as bacteria, yeast, worms, flies and mice), development of new technologies for biological and medical research, computational methods to analyze genomes, and ethical, legal and social issues related to genetics.

The sixteen institutions that form the International Human Genome Sequencing Consortium include:

Baylor College of Medicine, Houston, Texas, USA
Beijing Human Genome Center, Institute of Genetics, Chinese Academy of Sciences, Beijing, China
Gesellschaft fur Biotechnologische Forschung mbH, Braunschweig, Germany
Genoscope, Evry, France
Genome Therapeutics Corporation, Waltham, MA, USA
Institute for Molecular Biotechnology, Jena, Germany
Joint Genome Institute, U.S. Department of Energy, Walnut Creek, CA, USA
Keio University, Tokyo, Japan
Max Planck Institute for Molecular Genetics, Berlin, Germany
RIKEN Genomic Sciences Center, Saitama, Japan
The Sanger Centre, Hinxton, U.K.
Stanford DNA Sequencing and Technology Development Center, Palo Alto, CA, USA
University of Washington Genome Center, Seattle, WA, USA
University of Washington Multimegabase Sequencing Center, Seattle, WA, USA
Whitehead Institute for Biomedical Research, MIT, Cambridge, MA, USA
Washington University Genome Sequencing Center, St. Louis, MO, USA

In addition, two institutions played a key role in providing computational support and analysis for the HGP over the course of the past eighteen months. These include:

The National Center for Biotechnology Information at NIH
The European Bioinformatics Institute in Cambridge, UK

Scientists at the University of California, Santa Cruz, and Neomorphic, Inc. also assisted the assembly of the genome sequence across chromosomes,

Genome Sequencing Center Media Contacts

Baylor College of Medicine
Dorey A. Zodrow	Lynn Foltin
713-798-7965	713-798-4712
Pager: (800) 609-9162	Pager: (713) 905-4239
E-mail: dzodrow@bcm.tmc.edu	E-mail: jfoltin@bcm.tmc.edu
The Sanger Centre
Don Powell	Noorece Ahmed
Phone: 44-1223-494956	Phone: 44-171-611-8540
E-mail: don@sanger.ac.uk	E-mail: n.ahmed@wellcome.ac.uk
U.S. Department of Energy Joint Genome Institute
Jeff Sherwood	Steve Wampler
Phone: (202) 586-5823	Phone: (925) 423-3107
E-mail: jeff.sherwood@hq.doe.gov	E-mail: ampler1@llnl.gov
Ron Kolb	Sarah Wenning
Phone: (510) 486-7586	Phone: (925) 296-5608
E-mail: RRKolb@lbl.gov	E-mail: Wenning1@llnl.gov
Washington University School of Medicine in St. Louis
Joni Westerhouse	Nicole Vines
Phone: (314) 286-0120	Phone: (314) 286-0105
Pager: (314) 407-3566	Pager: (314) 670-5815
E-mail: joniw@medicine.wustl.edu	E-mail: vinesn@medicine.wustl.edu
Whitehead Institute for Biomedical Research
Seema Kumar	Eve Nichols
Phone: (617) 258-6153	Phone: (617) 258-7160
E-mail: kumar@wi.mit.edu	E-mail: nichols@wi.mit.edu

Contact:
Cathy Yarbrough
NHGRI

April Thompson
NHGRI

Last updated: September 03, 2013