We describe here a transposon-based DNA sequencing strategy that allows the introduction of sequencing priming sites throughout a target sequence by bacterial mating. A miniplasmid was designed to select against transposon insertions into the vector. Sites of transposon insertion are mapped by the polymerase chain reaction with bacterial overnight cultures providing the templates. A small set of plasmids with transposons spaced several hundred base pairs apart can then be sequenced. Sequencing primers corresponding to the transposon ends allow sequencing in both directions. Thus, the entire sequence of both strands can be easily determined
We describe a method of screening for transposon insertions in or near Drosophila loci that correspo...
We describe a simple PCR-based method for the isolation of genomic DNA that lies adjacent to a known...
DNA cloning is often used to select and amplify one DNA species from a mixture. However, the cloning...
Plasposons are modified mini-Tn5 transposons for random mutagenesis of Gram-negative bacteria. Their...
This chapter introduces a set of transposon-based methods that were developed to sample trinucleotid...
Abstract only availableTn5 transposon mutagenesis occurs by a mechanism in which a segment of DNA (t...
Bacterial transposons propagate through either non-replicative (cut-and-paste) or replicative (copy-...
Transposon insertion site sequencing (TIS) is a powerful method for associating genotype to phenotyp...
Abstract only availableTn5 transposon mutagenesis occurs by a mechanism in which a segment of DNA (t...
A rapid and simple method to amplify genomic DNA sequences flanking mini-Tn5 transposon insertion wa...
A procedure is presented, that has allowed the rapid assignment of transposon Tn1 and Tn7 insertion ...
<p>A. A Mtb mutant library is created by phage-delivery of transposons, disrupting each genome with ...
A method for obtaining well-defined deletions in an octopine Ti plasmid was developed. It was based ...
Cut-and-paste DNA transposons of the mariner/Tc1 family are useful tools for genome engineering and ...
The plasmid DNA is cleaved with an enzyme and joined in vitro to foreign DNA; the resulting recombin...
We describe a method of screening for transposon insertions in or near Drosophila loci that correspo...
We describe a simple PCR-based method for the isolation of genomic DNA that lies adjacent to a known...
DNA cloning is often used to select and amplify one DNA species from a mixture. However, the cloning...
Plasposons are modified mini-Tn5 transposons for random mutagenesis of Gram-negative bacteria. Their...
This chapter introduces a set of transposon-based methods that were developed to sample trinucleotid...
Abstract only availableTn5 transposon mutagenesis occurs by a mechanism in which a segment of DNA (t...
Bacterial transposons propagate through either non-replicative (cut-and-paste) or replicative (copy-...
Transposon insertion site sequencing (TIS) is a powerful method for associating genotype to phenotyp...
Abstract only availableTn5 transposon mutagenesis occurs by a mechanism in which a segment of DNA (t...
A rapid and simple method to amplify genomic DNA sequences flanking mini-Tn5 transposon insertion wa...
A procedure is presented, that has allowed the rapid assignment of transposon Tn1 and Tn7 insertion ...
<p>A. A Mtb mutant library is created by phage-delivery of transposons, disrupting each genome with ...
A method for obtaining well-defined deletions in an octopine Ti plasmid was developed. It was based ...
Cut-and-paste DNA transposons of the mariner/Tc1 family are useful tools for genome engineering and ...
The plasmid DNA is cleaved with an enzyme and joined in vitro to foreign DNA; the resulting recombin...
We describe a method of screening for transposon insertions in or near Drosophila loci that correspo...
We describe a simple PCR-based method for the isolation of genomic DNA that lies adjacent to a known...
DNA cloning is often used to select and amplify one DNA species from a mixture. However, the cloning...