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Exoquence DNA sequencing
Author(s) -
Chuan Li,
Philip W. Tucker
Publication year - 1993
Publication title -
nucleic acids research
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/21.5.1239
Subject(s) - sequencing by ligation , biology , sequencing by hybridization , dna nanoball sequencing , dna sequencing , oligonucleotide , primer (cosmetics) , dna , massive parallel sequencing , primer dimer , exonuclease iii , multiple displacement amplification , computational biology , restriction enzyme , subcloning , sequence assembly , genetics , genomic library , dna extraction , polymerase chain reaction , base sequence , plasmid , gene , dna sequencer , multiplex polymerase chain reaction , transcriptome , chemistry , gene expression , organic chemistry , escherichia coli
We have developed a strategy for DNA sequencing based on exonuclease III digestion followed by double strand specific endonuclease digestion and direct dideoxynucleotide sequencing reaction. This strategy eliminates the need for subcloning, oligonucleotide primers, and prior knowledge of the DNA to be sequenced. All template and primer duplexes needed for sequencing a complete insert can be prepared in one day from uncharacterized starting DNA. Sequence information can be obtained from different regions of the DNA simultaneously. The method uses double-stranded DNA to generate single-stranded template and primer, and thus produces high quality sequence results. Commercially available dideoxy-sequencing kits are well suited for this method. The strategy should be applicable for both automatic and routine laboratory DNA sequencing.

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