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Genomic sequencing.

Proceedings of the National Academy of Sciences · 1984 · Vol. 81(7) · pp. 1991–1995
George M. ChurchW Gilbert

Abstract

Unique DNA sequences can be determined directly from mouse genomic DNA. A denaturing gel separates by size mixtures of unlabeled DNA fragments from complete restriction and partial chemical cleavages of the entire genome. These lanes of DNA are transferred and UV-crosslinked to nylon membranes. Hybridization with a short 32P-labeled single-stranded probe produces the image of a DNA sequence "ladder" extending from the 3' or 5' end of one restriction site in the genome. Numerous different sequences can be obtained from a single membrane by reprobing. Each band in these sequences represents 3 fg of DNA complementary to the probe. Sequence data from mouse immunoglobulin heavy chain genes from several cell types are presented. The genomic sequencing procedures are applicable to the analysis of genetic polymorphisms, DNA methylation at deoxycytidines, and nucleic acid-protein interactions at single nucleotide resolution.

DNA and Nucleic Acid ChemistryDNA Repair MechanismsRNA modifications and cancerDNA nanoball sequencingSequencing by hybridizationDNABiologyGenomeDNA sequencinggenomic DNAGeneticsSequencing by ligationNucleic acid

MeSH terms

AnimalsBase SequenceDNADNA Restriction EnzymesGenesImmunoglobulin Heavy ChainsMethylationNucleic Acid DenaturationNucleic Acid HybridizationDNA-Directed RNA PolymerasesMice

Funding

  • Biogen
  • National Institutes of Health
Citations
8,225
FWCI
68.32
field-weighted impact
References
35
Percentile
100%
vs. same field & year
Citations per year
References
Detection of specific sequences among DNA fragments separated by gel electrophoresis
Journal of Molecular Biology · 1975 · 32,825 citations
Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose.
Proceedings of the National Academy of Sciences · 1980 · 8,386 citations
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