
We describe here a new strategy of fragment preparation for sequencing procedures using endlabelled DNA fragments as substrates (2,3) which is directly applicable to DNA fragments cloned into the Pst I site of pBR322, or in modified form, to inserts into the BamH I or Sal I site of the same plasmid. Ordered sets of subclones of predetermined overlap are are generated. These can be sequenced directly without further strand- or fragment separation steps.
DNA, Bacterial, Base Sequence, DNA, Viral, DNA, Recombinant, Escherichia coli, Methods, DNA Restriction Enzymes, Cloning, Molecular, Semliki forest virus, Plasmids
DNA, Bacterial, Base Sequence, DNA, Viral, DNA, Recombinant, Escherichia coli, Methods, DNA Restriction Enzymes, Cloning, Molecular, Semliki forest virus, Plasmids
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| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
