Literature DB >> 10591208

The DNA sequence of human chromosome 22.

I Dunham1, N Shimizu, B A Roe, S Chissoe, A R Hunt, J E Collins, R Bruskiewich, D M Beare, M Clamp, L J Smink, R Ainscough, J P Almeida, A Babbage, C Bagguley, J Bailey, K Barlow, K N Bates, O Beasley, C P Bird, S Blakey, A M Bridgeman, D Buck, J Burgess, W D Burrill, K P O'Brien.   

Abstract

Knowledge of the complete genomic DNA sequence of an organism allows a systematic approach to defining its genetic components. The genomic sequence provides access to the complete structures of all genes, including those without known function, their control elements, and, by inference, the proteins they encode, as well as all other biologically important sequences. Furthermore, the sequence is a rich and permanent source of information for the design of further biological studies of the organism and for the study of evolution through cross-species sequence comparison. The power of this approach has been amply demonstrated by the determination of the sequences of a number of microbial and model organisms. The next step is to obtain the complete sequence of the entire human genome. Here we report the sequence of the euchromatic part of human chromosome 22. The sequence obtained consists of 12 contiguous segments spanning 33.4 megabases, contains at least 545 genes and 134 pseudogenes, and provides the first view of the complex chromosomal landscapes that will be found in the rest of the genome.

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Year:  1999        PMID: 10591208     DOI: 10.1038/990031

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  247 in total

1.  A SNP resource for human chromosome 22: extracting dense clusters of SNPs from the genomic sequence.

Authors:  E Dawson; Y Chen; S Hunt; L J Smink; A Hunt; K Rice; S Livingston; S Bumpstead; R Bruskiewich; P Sham; R Ganske; M Adams; K Kawasaki; N Shimizu; S Minoshima; B Roe; D Bentley; I Dunham
Journal:  Genome Res       Date:  2001-01       Impact factor: 9.043

2.  The Molecular Biology Database Collection: an updated compilation of biological database resources.

Authors:  A D Baxevanis
Journal:  Nucleic Acids Res       Date:  2001-01-01       Impact factor: 16.971

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4.  Genome-scale compositional comparisons in eukaryotes.

Authors:  A J Gentles; S Karlin
Journal:  Genome Res       Date:  2001-04       Impact factor: 9.043

5.  Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing.

Authors:  J C Simpson; R Wellenreuther; A Poustka; R Pepperkok; S Wiemann
Journal:  EMBO Rep       Date:  2000-09       Impact factor: 8.807

6.  Complex mtDNA constitutes an approximate 620-kb insertion on Arabidopsis thaliana chromosome 2: implication of potential sequencing errors caused by large-unit repeats.

Authors:  R M Stupar; J W Lilly; C D Town; Z Cheng; S Kaul; C R Buell; J Jiang
Journal:  Proc Natl Acad Sci U S A       Date:  2001-04-17       Impact factor: 11.205

7.  Evolution of the rodent eosinophil-associated RNase gene family by rapid gene sorting and positive selection.

Authors:  J Zhang; K D Dyer; H F Rosenberg
Journal:  Proc Natl Acad Sci U S A       Date:  2000-04-25       Impact factor: 11.205

8.  A fast and scalable radiation hybrid map construction and integration strategy.

Authors:  R Agarwala; D L Applegate; D Maglott; G D Schuler; A A Schäffer
Journal:  Genome Res       Date:  2000-03       Impact factor: 9.043

9.  The gene for May-Hegglin anomaly localizes to a <1-Mb region on chromosome 22q12.3-13.1.

Authors:  J A Martignetti; K E Heath; J Harris; N Bizzaro; A Savoia; C L Balduini; R J Desnick
Journal:  Am J Hum Genet       Date:  2000-03-17       Impact factor: 11.025

10.  Waiting for the working draft from the human genome project. A huge achievement, but not of immediate medical use.

Authors:  L R Cardon; H Watkins
Journal:  BMJ       Date:  2000-05-06
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