The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X
D. R. Bentley (),
P. Deloukas,
A. Dunham,
L. French,
S. G. Gregory,
S. J. Humphray,
A. J. Mungall,
M. T. Ross,
N. P. Carter,
I. Dunham,
C. E. Scott,
K. J. Ashcroft,
A. L. Atkinson,
K. Aubin,
D. M. Beare,
G. Bethel,
N. Brady,
J. C. Brook,
D. C. Burford,
W. D. Burrill,
C. Burrows,
A. P. Butler,
C. Carder,
J. J. Catanese,
C. M. Clee,
S. M. Clegg,
V. Cobley,
A. J. Coffey,
C. G. Cole,
J. E. Collins,
J. S. Conquer,
R. A. Cooper,
K. M. Culley,
E. Dawson,
F. L. Dearden,
R. M. Durbin,
P. J. de Jong,
P. D. Dhami,
M. E. Earthrowl,
C. A. Edwards,
R. S. Evans,
C. J. Gillson,
J. Ghori,
L. Green,
R. Gwilliam,
K. S. Halls,
S. Hammond,
G. L. Harper,
R. W. Heathcott,
J. L. Holden,
E. Holloway,
B. L. Hopkins,
P. J. Howard,
G. R. Howell,
E. J. Huckle,
J. Hughes,
P. J. Hunt,
S. E. Hunt,
M. Izmajlowicz,
C. A. Jones,
S. S. Joseph,
G. Laird,
C. F. Langford,
M. H. Lehvaslaiho,
M. A. Leversha,
O. T. McCann,
L. M. McDonald,
J. McDowall,
G. L. Maslen,
D. Mistry,
N. K. Moschonas,
V. Neocleous,
D. M. Pearson,
K. J. Phillips,
K. M. Porter,
S. R. Prathalingam,
Y. H. Ramsey,
S. A. Ranby,
C. M. Rice,
J. Rogers,
L. J. Rogers,
T. Sarafidou,
D. J. Scott,
G. J. Sharp,
C. J. Shaw-Smith,
L. J. Smink,
C. Soderlund,
E. C. Sotheran,
H. E. Steingruber,
J. E. Sulston,
A. Taylor,
R. G. Taylor,
A. A. Thorpe,
E. Tinsley,
G. L. Warry,
A. Whittaker,
P. Whittaker,
S. H. Williams,
T. E. Wilmer,
R. Wooster and
C. L. Wright
Additional contact information
D. R. Bentley: The Sanger Centre, Wellcome Trust Genome Campus
P. Deloukas: The Sanger Centre, Wellcome Trust Genome Campus
A. Dunham: The Sanger Centre, Wellcome Trust Genome Campus
L. French: The Sanger Centre, Wellcome Trust Genome Campus
S. G. Gregory: The Sanger Centre, Wellcome Trust Genome Campus
S. J. Humphray: The Sanger Centre, Wellcome Trust Genome Campus
A. J. Mungall: The Sanger Centre, Wellcome Trust Genome Campus
M. T. Ross: The Sanger Centre, Wellcome Trust Genome Campus
N. P. Carter: The Sanger Centre, Wellcome Trust Genome Campus
I. Dunham: The Sanger Centre, Wellcome Trust Genome Campus
C. E. Scott: The Sanger Centre, Wellcome Trust Genome Campus
K. J. Ashcroft: The Sanger Centre, Wellcome Trust Genome Campus
A. L. Atkinson: The Sanger Centre, Wellcome Trust Genome Campus
K. Aubin: The Sanger Centre, Wellcome Trust Genome Campus
D. M. Beare: The Sanger Centre, Wellcome Trust Genome Campus
G. Bethel: The Sanger Centre, Wellcome Trust Genome Campus
N. Brady: The Sanger Centre, Wellcome Trust Genome Campus
J. C. Brook: The Sanger Centre, Wellcome Trust Genome Campus
D. C. Burford: The Sanger Centre, Wellcome Trust Genome Campus
W. D. Burrill: The Sanger Centre, Wellcome Trust Genome Campus
C. Burrows: The Sanger Centre, Wellcome Trust Genome Campus
A. P. Butler: The Sanger Centre, Wellcome Trust Genome Campus
C. Carder: The Sanger Centre, Wellcome Trust Genome Campus
J. J. Catanese: Children's Hospital-BACPAC Resources
C. M. Clee: The Sanger Centre, Wellcome Trust Genome Campus
S. M. Clegg: The Sanger Centre, Wellcome Trust Genome Campus
V. Cobley: The Sanger Centre, Wellcome Trust Genome Campus
A. J. Coffey: The Sanger Centre, Wellcome Trust Genome Campus
C. G. Cole: The Sanger Centre, Wellcome Trust Genome Campus
J. E. Collins: The Sanger Centre, Wellcome Trust Genome Campus
J. S. Conquer: The Sanger Centre, Wellcome Trust Genome Campus
R. A. Cooper: The Sanger Centre, Wellcome Trust Genome Campus
K. M. Culley: The Sanger Centre, Wellcome Trust Genome Campus
E. Dawson: The Sanger Centre, Wellcome Trust Genome Campus
F. L. Dearden: The Sanger Centre, Wellcome Trust Genome Campus
R. M. Durbin: The Sanger Centre, Wellcome Trust Genome Campus
P. J. de Jong: Children's Hospital-BACPAC Resources
P. D. Dhami: The Sanger Centre, Wellcome Trust Genome Campus
M. E. Earthrowl: The Sanger Centre, Wellcome Trust Genome Campus
C. A. Edwards: The Sanger Centre, Wellcome Trust Genome Campus
R. S. Evans: The Sanger Centre, Wellcome Trust Genome Campus
C. J. Gillson: The Sanger Centre, Wellcome Trust Genome Campus
J. Ghori: The Sanger Centre, Wellcome Trust Genome Campus
L. Green: The Sanger Centre, Wellcome Trust Genome Campus
R. Gwilliam: The Sanger Centre, Wellcome Trust Genome Campus
K. S. Halls: The Sanger Centre, Wellcome Trust Genome Campus
S. Hammond: The Sanger Centre, Wellcome Trust Genome Campus
G. L. Harper: The Sanger Centre, Wellcome Trust Genome Campus
R. W. Heathcott: The Sanger Centre, Wellcome Trust Genome Campus
J. L. Holden: The Sanger Centre, Wellcome Trust Genome Campus
E. Holloway: The Sanger Centre, Wellcome Trust Genome Campus
B. L. Hopkins: The Sanger Centre, Wellcome Trust Genome Campus
P. J. Howard: The Sanger Centre, Wellcome Trust Genome Campus
G. R. Howell: The Sanger Centre, Wellcome Trust Genome Campus
E. J. Huckle: The Sanger Centre, Wellcome Trust Genome Campus
J. Hughes: The Sanger Centre, Wellcome Trust Genome Campus
P. J. Hunt: The Sanger Centre, Wellcome Trust Genome Campus
S. E. Hunt: The Sanger Centre, Wellcome Trust Genome Campus
M. Izmajlowicz: The Sanger Centre, Wellcome Trust Genome Campus
C. A. Jones: The Sanger Centre, Wellcome Trust Genome Campus
S. S. Joseph: The Sanger Centre, Wellcome Trust Genome Campus
G. Laird: The Sanger Centre, Wellcome Trust Genome Campus
C. F. Langford: The Sanger Centre, Wellcome Trust Genome Campus
M. H. Lehvaslaiho: The Sanger Centre, Wellcome Trust Genome Campus
M. A. Leversha: The Sanger Centre, Wellcome Trust Genome Campus
O. T. McCann: The Sanger Centre, Wellcome Trust Genome Campus
L. M. McDonald: The Sanger Centre, Wellcome Trust Genome Campus
J. McDowall: The Sanger Centre, Wellcome Trust Genome Campus
G. L. Maslen: The Sanger Centre, Wellcome Trust Genome Campus
D. Mistry: The Sanger Centre, Wellcome Trust Genome Campus
N. K. Moschonas: University of Crete and Institute of Molecular Biology and Biotechnology
V. Neocleous: Neurogenetic Laboratory, The Cyprus Institute of Neurology and Genetics
D. M. Pearson: The Sanger Centre, Wellcome Trust Genome Campus
K. J. Phillips: The Sanger Centre, Wellcome Trust Genome Campus
K. M. Porter: The Sanger Centre, Wellcome Trust Genome Campus
S. R. Prathalingam: The Sanger Centre, Wellcome Trust Genome Campus
Y. H. Ramsey: The Sanger Centre, Wellcome Trust Genome Campus
S. A. Ranby: The Sanger Centre, Wellcome Trust Genome Campus
C. M. Rice: The Sanger Centre, Wellcome Trust Genome Campus
J. Rogers: The Sanger Centre, Wellcome Trust Genome Campus
L. J. Rogers: The Sanger Centre, Wellcome Trust Genome Campus
T. Sarafidou: University of Crete and Institute of Molecular Biology and Biotechnology
D. J. Scott: The Sanger Centre, Wellcome Trust Genome Campus
G. J. Sharp: The Sanger Centre, Wellcome Trust Genome Campus
C. J. Shaw-Smith: The Sanger Centre, Wellcome Trust Genome Campus
L. J. Smink: The Sanger Centre, Wellcome Trust Genome Campus
C. Soderlund: The Sanger Centre, Wellcome Trust Genome Campus
E. C. Sotheran: The Sanger Centre, Wellcome Trust Genome Campus
H. E. Steingruber: The Sanger Centre, Wellcome Trust Genome Campus
J. E. Sulston: The Sanger Centre, Wellcome Trust Genome Campus
A. Taylor: The Sanger Centre, Wellcome Trust Genome Campus
R. G. Taylor: The Sanger Centre, Wellcome Trust Genome Campus
A. A. Thorpe: The Sanger Centre, Wellcome Trust Genome Campus
E. Tinsley: The Sanger Centre, Wellcome Trust Genome Campus
G. L. Warry: The Sanger Centre, Wellcome Trust Genome Campus
A. Whittaker: The Sanger Centre, Wellcome Trust Genome Campus
P. Whittaker: The Sanger Centre, Wellcome Trust Genome Campus
S. H. Williams: The Sanger Centre, Wellcome Trust Genome Campus
T. E. Wilmer: The Sanger Centre, Wellcome Trust Genome Campus
R. Wooster: The Sanger Centre, Wellcome Trust Genome Campus
C. L. Wright: The Sanger Centre, Wellcome Trust Genome Campus
Nature, 2001, vol. 409, issue 6822, 942-943
Abstract:
Abstract We constructed maps for eight chromosomes (1, 6, 9, 10, 13, 20, X and (previously) 22), representing one-third of the genome, by building landmark maps, isolating bacterial clones and assembling contigs. By this approach, we could establish the long-range organization of the maps early in the project, and all contig extension, gap closure and problem-solving was simplified by containment within local regions. The maps currently represent more than 94% of the euchromatic (gene-containing) regions of these chromosomes in 176 contigs, and contain 96% of the chromosome-specific markers in the human gene map. By measuring the remaining gaps, we can assess chromosome length and coverage in sequenced clones.
Date: 2001
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DOI: 10.1038/35057165
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