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Science 16 February 2001: Vol. 291. no. 5507, pp. 1304 - 1351 DOI: 10.1126/science.1058040
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Review
The Sequence of the Human Genome
J. Craig Venter,1*
Mark D. Adams,1
Eugene W. Myers,1
Peter W. Li,1
Richard J. Mural,1
Granger G. Sutton,1
Hamilton O. Smith,1
Mark Yandell,1
Cheryl A. Evans,1
Robert A. Holt,1
Jeannine D. Gocayne,1
Peter Amanatides,1
Richard M. Ballew,1
Daniel H. Huson,1
Jennifer Russo Wortman,1
Qing Zhang,1
Chinnappa D. Kodira,1
Xiangqun H. Zheng,1
Lin Chen,1
Marian Skupski,1
Gangadharan Subramanian,1
Paul D. Thomas,1
Jinghui Zhang,1
George L. Gabor Miklos,2
Catherine Nelson,3
Samuel Broder,1
Andrew G. Clark,4
Joe Nadeau,5
Victor A. McKusick,6
Norton Zinder,7
Arnold J. Levine,7
Richard J. Roberts,8
Mel Simon,9
Carolyn Slayman,10
Michael Hunkapiller,11
Randall Bolanos,1
Arthur Delcher,1
Ian Dew,1
Daniel Fasulo,1
Michael Flanigan,1
Liliana Florea,1
Aaron Halpern,1
Sridhar Hannenhalli,1
Saul Kravitz,1
Samuel Levy,1
Clark Mobarry,1
Knut Reinert,1
Karin Remington,1
Jane Abu-Threideh,1
Ellen Beasley,1
Kendra Biddick,1
Vivien Bonazzi,1
Rhonda Brandon,1
Michele Cargill,1
Ishwar Chandramouliswaran,1
Rosane Charlab,1
Kabir Chaturvedi,1
Zuoming Deng,1
Valentina Di Francesco,1
Patrick Dunn,1
Karen Eilbeck,1
Carlos Evangelista,1
Andrei E. Gabrielian,1
Weiniu Gan,1
Wangmao Ge,1
Fangcheng Gong,1
Zhiping Gu,1
Ping Guan,1
Thomas J. Heiman,1
Maureen E. Higgins,1
Rui-Ru Ji,1
Zhaoxi Ke,1
Karen A. Ketchum,1
Zhongwu Lai,1
Yiding Lei,1
Zhenya Li,1
Jiayin Li,1
Yong Liang,1
Xiaoying Lin,1
Fu Lu,1
Gennady V. Merkulov,1
Natalia Milshina,1
Helen M. Moore,1
Ashwinikumar K Naik,1
Vaibhav A. Narayan,1
Beena Neelam,1
Deborah Nusskern,1
Douglas B. Rusch,1
Steven Salzberg,12
Wei Shao,1
Bixiong Shue,1
Jingtao Sun,1
Zhen Yuan Wang,1
Aihui Wang,1
Xin Wang,1
Jian Wang,1
Ming-Hui Wei,1
Ron Wides,13
Chunlin Xiao,1
Chunhua Yan,1
Alison Yao,1
Jane Ye,1
Ming Zhan,1
Weiqing Zhang,1
Hongyu Zhang,1
Qi Zhao,1
Liansheng Zheng,1
Fei Zhong,1
Wenyan Zhong,1
Shiaoping C. Zhu,1
Shaying Zhao,12
Dennis Gilbert,1
Suzanna Baumhueter,1
Gene Spier,1
Christine Carter,1
Anibal Cravchik,1
Trevor Woodage,1
Feroze Ali,1
Huijin An,1
Aderonke Awe,1
Danita Baldwin,1
Holly Baden,1
Mary Barnstead,1
Ian Barrow,1
Karen Beeson,1
Dana Busam,1
Amy Carver,1
Angela Center,1
Ming Lai Cheng,1
Liz Curry,1
Steve Danaher,1
Lionel Davenport,1
Raymond Desilets,1
Susanne Dietz,1
Kristina Dodson,1
Lisa Doup,1
Steven Ferriera,1
Neha Garg,1
Andres Gluecksmann,1
Brit Hart,1
Jason Haynes,1
Charles Haynes,1
Cheryl Heiner,1
Suzanne Hladun,1
Damon Hostin,1
Jarrett Houck,1
Timothy Howland,1
Chinyere Ibegwam,1
Jeffery Johnson,1
Francis Kalush,1
Lesley Kline,1
Shashi Koduru,1
Amy Love,1
Felecia Mann,1
David May,1
Steven McCawley,1
Tina McIntosh,1
Ivy McMullen,1
Mee Moy,1
Linda Moy,1
Brian Murphy,1
Keith Nelson,1
Cynthia Pfannkoch,1
Eric Pratts,1
Vinita Puri,1
Hina Qureshi,1
Matthew Reardon,1
Robert Rodriguez,1
Yu-Hui Rogers,1
Deanna Romblad,1
Bob Ruhfel,1
Richard Scott,1
Cynthia Sitter,1
Michelle Smallwood,1
Erin Stewart,1
Renee Strong,1
Ellen Suh,1
Reginald Thomas,1
Ni Ni Tint,1
Sukyee Tse,1
Claire Vech,1
Gary Wang,1
Jeremy Wetter,1
Sherita Williams,1
Monica Williams,1
Sandra Windsor,1
Emily Winn-Deen,1
Keriellen Wolfe,1
Jayshree Zaveri,1
Karena Zaveri,1
Josep F. Abril,14
Roderic Guigó,14
Michael J. Campbell,1
Kimmen V. Sjolander,1
Brian Karlak,1
Anish Kejariwal,1
Huaiyu Mi,1
Betty Lazareva,1
Thomas Hatton,1
Apurva Narechania,1
Karen Diemer,1
Anushya Muruganujan,1
Nan Guo,1
Shinji Sato,1
Vineet Bafna,1
Sorin Istrail,1
Ross Lippert,1
Russell Schwartz,1
Brian Walenz,1
Shibu Yooseph,1
David Allen,1
Anand Basu,1
James Baxendale,1
Louis Blick,1
Marcelo Caminha,1
John Carnes-Stine,1
Parris Caulk,1
Yen-Hui Chiang,1
My Coyne,1
Carl Dahlke,1
Anne Deslattes Mays,1
Maria Dombroski,1
Michael Donnelly,1
Dale Ely,1
Shiva Esparham,1
Carl Fosler,1
Harold Gire,1
Stephen Glanowski,1
Kenneth Glasser,1
Anna Glodek,1
Mark Gorokhov,1
Ken Graham,1
Barry Gropman,1
Michael Harris,1
Jeremy Heil,1
Scott Henderson,1
Jeffrey Hoover,1
Donald Jennings,1
Catherine Jordan,1
James Jordan,1
John Kasha,1
Leonid Kagan,1
Cheryl Kraft,1
Alexander Levitsky,1
Mark Lewis,1
Xiangjun Liu,1
John Lopez,1
Daniel Ma,1
William Majoros,1
Joe McDaniel,1
Sean Murphy,1
Matthew Newman,1
Trung Nguyen,1
Ngoc Nguyen,1
Marc Nodell,1
Sue Pan,1
Jim Peck,1
Marshall Peterson,1
William Rowe,1
Robert Sanders,1
John Scott,1
Michael Simpson,1
Thomas Smith,1
Arlan Sprague,1
Timothy Stockwell,1
Russell Turner,1
Eli Venter,1
Mei Wang,1
Meiyuan Wen,1
David Wu,1
Mitchell Wu,1
Ashley Xia,1
Ali Zandieh,1
Xiaohong Zhu1
A 2.91-billion base pair (bp) consensus sequence of the euchromatic
portion of the human genome was generated by the whole-genome shotgun
sequencing method. The 14.8-billion bp DNA sequence was generated over
9 months from 27,271,853 high-quality sequence reads (5.11-fold
coverage of the genome) from both ends of plasmid clones made from the
DNA of five individuals. Two assembly strategies--a whole-genome
assembly and a regional chromosome assembly--were used, each combining
sequence data from Celera and the publicly funded genome effort. The
public data were shredded into 550-bp segments to create a 2.9-fold
coverage of those genome regions that had been sequenced, without
including biases inherent in the cloning and assembly procedure used by
the publicly funded group. This brought the effective coverage in the
assemblies to eightfold, reducing the number and size of gaps in the
final assembly over what would be obtained with 5.11-fold coverage. The
two assembly strategies yielded very similar results that largely agree
with independent mapping data. The assemblies effectively cover the euchromatic regions of the human chromosomes. More than 90% of the
genome is in scaffold assemblies of 100,000 bp or more, and 25% of the
genome is in scaffolds of 10 million bp or larger. Analysis of the
genome sequence revealed 26,588 protein-encoding transcripts for which
there was strong corroborating evidence and an additional ~12,000
computationally derived genes with mouse matches or other weak
supporting evidence. Although gene-dense clusters are obvious, almost
half the genes are dispersed in low G+C sequence separated by large
tracts of apparently noncoding sequence. Only 1.1% of the genome is
spanned by exons, whereas 24% is in introns, with 75% of the genome
being intergenic DNA. Duplications of segmental blocks, ranging in size
up to chromosomal lengths, are abundant throughout the genome and
reveal a complex evolutionary history. Comparative genomic analysis
indicates vertebrate expansions of genes associated with neuronal
function, with tissue-specific developmental regulation, and with the
hemostasis and immune systems. DNA sequence comparisons between the
consensus sequence and publicly funded genome data provided locations
of 2.1 million single-nucleotide polymorphisms (SNPs). A random pair of
human haploid genomes differed at a rate of 1 bp per 1250 on average,
but there was marked heterogeneity in the level of polymorphism across
the genome. Less than 1% of all SNPs resulted in variation in
proteins, but the task of determining which SNPs have functional
consequences remains an open challenge.
1 Celera Genomics, 45 West Gude Drive,
Rockville, MD 20850, USA.
2 GenetixXpress, 78 Pacific Road, Palm Beach, Sydney 2108, Australia.
3 Berkeley Drosophila Genome Project,
University of California, Berkeley, CA 94720, USA.
4 Department of Biology, Penn State University, 208 Mueller Lab, University Park, PA 16802, USA.
5 Department of Genetics, Case Western Reserve
University School of Medicine, BRB-630, 10900 Euclid Avenue, Cleveland,
OH 44106, USA.
6 Johns Hopkins University School of
Medicine, Johns Hopkins Hospital, 600 North Wolfe Street, Blalock 1007, Baltimore, MD 21287-4922, USA.
7 Rockefeller
University, 1230 York Avenue, New York, NY 10021-6399, USA.
8 New England BioLabs, 32 Tozer Road, Beverly, MA
01915, USA.
9 Division of Biology, 147-75, California Institute of Technology, 1200 East California Boulevard,
Pasadena, CA 91125, USA.
10 Yale University School
of Medicine, 333 Cedar Street, P.O. Box 208000, New Haven, CT
06520-8000, USA.
11 Applied Biosystems, 850 Lincoln Centre Drive, Foster City, CA 94404, USA.
12 The Institute for Genomic Research, 9712 Medical
Center Drive, Rockville, MD 20850, USA.
13 Faculty
of Life Sciences, Bar-Ilan University, Ramat-Gan, 52900 Israel.
14 Grup de Recerca en Informàtica
Mèdica, Institut Municipal d'Investigació Mèdica,
Universitat Pompeu Fabra, 08003-Barcelona, Catalonia, Spain.
*
To whom correspondence should be addressed. E-mail:
humangenome{at}celera.com
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- DDBJ dealing with mass data produced by the second generation sequencer.
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Nucleic Acids Res.
37, D16-D18
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- Population Genetic Inference From Resequencing Data.
- R. Jiang, S. Tavare, and P. Marjoram (2009)
Genetics
181, 187-197
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- Synergy of Two Reference Genomes for the Grass Family.
- J. Messing (2009)
Plant Physiology
149, 117-124
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- SysPIMP: the web-based systematical platform for identifying human disease-related mutated sequences from mass spectrometry.
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Nucleic Acids Res.
37, D913-D920
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- The HuRef Browser: a web resource for individual human genomics.
- N. Axelrod, Y. Lin, P. C. Ng, T. B. Stockwell, J. Crabtree, J. Huang, E. Kirkness, R. L. Strausberg, M. E. Frazier, J. C. Venter, et al. (2009)
Nucleic Acids Res.
37, D1018-D1024
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- Bacteriophage Mu integration in yeast and mammalian genomes.
- A. O. Paatero, H. Turakainen, L. J. Happonen, C. Olsson, T. Palomaki, M. I. Pajunen, X. Meng, T. Otonkoski, T. Tuuri, C. Berry, et al. (2008)
Nucleic Acids Res.
36, e148
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- Seven Lipoprotein Lipase Gene Polymorphisms, Lipid Fractions, and Coronary Disease: A HuGE Association Review and Meta-Analysis.
- G. S. Sagoo, I. Tatt, G. Salanti, A. S. Butterworth, N. Sarwar, M. van Maarle, J. W. Jukema, B. Wiman, J. J. P. Kastelein, A. M. Bennet, et al. (2008)
Am. J. Epidemiol.
168, 1233-1246
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- A novel mechanistic spectrum underlies glaucoma-associated chromosome 6p25 copy number variation.
- B. Chanda, M. Asai-Coakwell, M. Ye, A. J. Mungall, M. Barrow, W. B. Dobyns, H. Behesti, J. C. Sowden, N. P. Carter, M. A. Walter, et al. (2008)
Hum. Mol. Genet.
17, 3446-3458
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- The Importance of Gene--Environment Interaction: Implications for Social Scientists.
- K. E. North and L. J. Martin (2008)
Sociological Methods Research
37, 164-200
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- Systems Epidemiology in Cancer.
- E. Lund and V. Dumeaux (2008)
Cancer Epidemiol. Biomarkers Prev.
17, 2954-2957
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- DNA Hypomethylation Arises Later in Prostate Cancer Progression than CpG Island Hypermethylation and Contributes to Metastatic Tumor Heterogeneity.
- S. Yegnasubramanian, M. C. Haffner, Y. Zhang, B. Gurel, T. C. Cornish, Z. Wu, R. A. Irizarry, J. Morgan, J. Hicks, T. L. DeWeese, et al. (2008)
Cancer Res.
68, 8954-8967
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- MELOE-1 is a new antigen overexpressed in melanomas and involved in adoptive T cell transfer efficiency.
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J. Exp. Med.
205, 2673-2682
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- Three tiers of genome evolution in reptiles.
- C. L. Organ, R. G. Moreno, and S. V. Edwards (2008)
Integr. Comp. Biol.
48, 494-504
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- Targeting the Human Cancer Pathway Protein Interaction Network by Structural Genomics.
- Y. J. Huang, D. Hang, L. J. Lu, L. Tong, M. B. Gerstein, and G. T. Montelione (2008)
Mol. Cell. Proteomics
7, 2048-2060
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- Curcumin Inhibits Lung Cancer Cell Invasion and Metastasis through the Tumor Suppressor HLJ1.
- H.-W. Chen, J.-Y. Lee, J.-Y. Huang, C.-C. Wang, W.-J. Chen, S.-F. Su, C.-W. Huang, C.-C. Ho, J. J.W. Chen, M.-F. Tsai, et al. (2008)
Cancer Res.
68, 7428-7438
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- The EuroPhysiome, STEP and a roadmap for the virtual physiological human.
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Phil Trans R Soc A
366, 2979-2999
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- Immunological Dominance of Trypanosoma cruzi Tandem Repeat Proteins.
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Infect. Immun.
76, 3967-3974
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- Advances in Chemical Carcinogenesis: A Historical Review and Prospective.
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Cancer Res.
68, 6863-6872
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- Development of a Homogeneous High-Throughput Live-Cell G-Protein-Coupled Receptor Binding Assay.
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J Biomol Screen
13, 748-754
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- A Homogeneous Enzyme Fragment Complementation-Based {beta}-Arrestin Translocation Assay for High-Throughput Screening of G-Protein-Coupled Receptors.
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J Biomol Screen
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