Literature DB >> 1577496

The generation of ordered sets of cosmid DNA clones from human chromosome region 11p.

I J Heding1, A C Ivens, J Wilson, M Strivens, S Gregory, J M Hoovers, M Mannens, B Redeker, D Porteous, V van Heyningen.   

Abstract

We describe progress in a continuing project aimed at the generation of an overlapping cosmid DNA clone map of the short arm of human chromosome 11. The automated procedures used to prepare DNA samples and the computerized data collection and recording systems are described. We also demonstrate the use of the clones as reagents for the rapid isolation of genomic DNAs containing smaller probed regions. We have isolated approximately 4700 human cosmid DNA clones from mouse/human hybrid cell lines that contain predominantly human chromosomal region 11p. Of the DNA in the cell lines, 60% is derived from this chromosomal region, and the remaining 40% is derived from regions of chromosomes 3, 19, and 20. A total of 4159 clones have been fingerprinted to identify potential overlaps, and we have developed 535 sets ("contigs"). Using random modeling, it is estimated that 65% of 11p must be contained in the analyzed cosmids. The database of clones has been used to identify single or overlapping clones from noncosmid DNA probes. Examples are presented. It is proposed that cosmid reference filters be distributed to requesting laboratories.

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Year:  1992        PMID: 1577496     DOI: 10.1016/0888-7543(92)90206-8

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  4 in total

1.  A 7.5 Mb sequence-ready PAC contig and gene expression map of human chromosome 11p13-p14.1.

Authors:  B Gawin; A Niederführ; N Schumacher; H Hummerich; P F Little; M Gessler
Journal:  Genome Res       Date:  1999-11       Impact factor: 9.043

2.  Genome mapping by fluorescent fingerprinting.

Authors:  S G Gregory; G R Howell; D R Bentley
Journal:  Genome Res       Date:  1997-12       Impact factor: 9.043

3.  Detection of a cryptic paracentric inversion within band 11p13 in familial aniridia by fluorescence in situ hybridization.

Authors:  Y Fukushima; J Hoovers; M Mannens; K Wakui; H Ohashi; T Ohno; Y Ueoka; N Niikawa
Journal:  Hum Genet       Date:  1993-04       Impact factor: 4.132

4.  Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.

Authors:  J M Hoovers; L M Kalikin; L A Johnson; M Alders; B Redeker; D J Law; J Bliek; M Steenman; M Benedict; J Wiegant; C Lengauer; P Taillon-Miller; D Schlessinger; M C Edwards; S J Elledge; A Ivens; A Westerveld; P Little; M Mannens; A P Feinberg
Journal:  Proc Natl Acad Sci U S A       Date:  1995-12-19       Impact factor: 11.205

  4 in total

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