| Literature DB >> 11237021 |
V G Cheung1, N Nowak, W Jang, I R Kirsch, S Zhao, X N Chen, T S Furey, U J Kim, W L Kuo, M Olivier, J Conroy, A Kasprzyk, H Massa, R Yonescu, S Sait, C Thoreen, A Snijders, E Lemyre, J A Bailey, A Bruzel, W D Burrill, S M Clegg, S Collins, P Dhami, C Friedman, C S Han, S Herrick, J Lee, A H Ligon, S Lowry, M Morley, S Narasimhan, K Osoegawa, Z Peng, I Plajzer-Frick, B J Quade, D Scott, K Sirotkin, A A Thorpe, J W Gray, J Hudson, D Pinkel, T Ried, L Rowen, G L Shen-Ong, R L Strausberg, E Birney, D F Callen, J F Cheng, D R Cox, N A Doggett, N P Carter, E E Eichler, D Haussler, J R Korenberg, C C Morton, D Albertson, G Schuler, P J de Jong, B J Trask.
Abstract
We have placed 7,600 cytogenetically defined landmarks on the draft sequence of the human genome to help with the characterization of genes altered by gross chromosomal aberrations that cause human disease. The landmarks are large-insert clones mapped to chromosome bands by fluorescence in situ hybridization. Each clone contains a sequence tag that is positioned on the genomic sequence. This genome-wide set of sequence-anchored clones allows structural and functional analyses of the genome. This resource represents the first comprehensive integration of cytogenetic, radiation hybrid, linkage and sequence maps of the human genome; provides an independent validation of the sequence map and framework for contig order and orientation; surveys the genome for large-scale duplications, which are likely to require special attention during sequence assembly; and allows a stringent assessment of sequence differences between the dark and light bands of chromosomes. It also provides insight into large-scale chromatin structure and the evolution of chromosomes and gene families and will accelerate our understanding of the molecular bases of human disease and cancer.Entities:
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Year: 2001 PMID： 11237021 PMCID： PMC7845515 DOI： 10.1038/35057192
Source DB: PubMed Journal: Nature ISSN： 0028-0836 Impact factor: 49.962