Genomic sequence sampling: a strategy for high resolution sequence–based physical mapping of complex genomes
- 1 May 1994
- journal article
- Published by Springer Nature in Nature Genetics
- Vol. 7 (1) , 40-47
- https://doi.org/10.1038/ng0594-40
Abstract
We present a simple and efficient method for constructing high resolution physical maps of large regions of genomic DNA based upon sampled sequencing. The physical map is constructed by ordering high density cosmid contigs and determining a sequence fragment from each end of every clone. The resulting map, which contains 30-50% of the complete DNA sequence, allows the identification of many genes and makes possible PCR amplification of virtually any part of the genome. We apply this strategy to the automated analysis of the genome of the primitive eukaryote Giardia lamblia and evaluate its applicability to the physical mapping and DNA sequencing of the human genome.Keywords
This publication has 54 references indexed in Scilit:
- A Sequence-Tagged Site Map of Human Chromosome 11Genomics, 1993
- DNA Sequence and Analysis of 136 Kilobases of the Escherichia coli Genome: Organizational Symmetry around the Origin of ReplicationGenomics, 1993
- DNA Sequence Determination by Hybridization: a Strategy for Efficient Large-Scale SequencingScience, 1993
- A cosmid contig and high resolution restriction map of the 2 megabase region containing the Huntington's disease geneNature Genetics, 1993
- Evaluation of a cosmid contig physical map of human chromosome 16Genomics, 1992
- Systematic generation of sequence-tagged sites for physical mapping of human chromosomes: Application to the mapping of human chromosome 7 using yeast artificial chromosomesGenomics, 1991
- Basic Local Alignment Search ToolJournal of Molecular Biology, 1990
- Basic local alignment search toolJournal of Molecular Biology, 1990
- Segmented α-helical coiled-coil structure of the protein giardin from the Giardia cytoskeletonJournal of Molecular Biology, 1988
- Separation of yeast chromosome-sized DNAs by pulsed field gradient gel electrophoresisCell, 1984