Transposon mutagenesis coupled to next-generation sequencing (TnSeq) is a powerful approach for discovering the functions of bacterial genes. However, the development of a suitable TnSeq strategy for a given bacterium can be costly and time-consuming. To meet this challenge, we describe a parts-based strategy for constructing libraries of hundreds of transposon delivery vectors, which we term “magic pools”. Within a magic pool, each transposon vector has a different combination of promoters and antibiotic resistance markers as well as a random DNA barcode sequence, which allows the tracking of each vector during mutagenesis experiments. To identify an efficient vector for a given bacterium, we mutagenize it with a magic pool and sequence th...
Transposons are invaluable biological tools for the genetic manipulation of microorganisms. ISY100 f...
Transposons are invaluable biological tools for the genetic manipulation of microorganisms. ISY100 f...
This work was supported by a Longer and Larger (LoLa) grant from the Biotechnology and Biological Sc...
Transposon mutagenesis coupled to next-generation sequencing (TnSeq) is a powerful approach for disc...
Transposon mutagenesis coupled to next-generation sequencing (TnSeq) is a powerful approach for disc...
Summary: Randomly barcoded transposon mutant libraries are powerful tools for studying gene function...
UnlabelledTransposon mutagenesis with next-generation sequencing (TnSeq) is a powerful approach to a...
UnlabelledTransposon mutagenesis with next-generation sequencing (TnSeq) is a powerful approach to a...
Random transposon mutagenesis allows for relatively rapid, genome-wide surveys to detect genes invol...
<p>A. A Mtb mutant library is created by phage-delivery of transposons, disrupting each genome with ...
Comprehensive mutant libraries can be readily constructed by transposon mutagenesis. To systematical...
Random transposon mutagenesis allows for relatively rapid, genome-wide surveys to detect genes invol...
Comprehensive mutant libraries can be readily constructed by transposon mutagenesis. To systematical...
Transposons are invaluable biological tools for the genetic manipulation of microorganisms. ISY100 f...
Re-programming microorganisms to modify their existing functions and/or to bestow bacteria with enti...
Transposons are invaluable biological tools for the genetic manipulation of microorganisms. ISY100 f...
Transposons are invaluable biological tools for the genetic manipulation of microorganisms. ISY100 f...
This work was supported by a Longer and Larger (LoLa) grant from the Biotechnology and Biological Sc...
Transposon mutagenesis coupled to next-generation sequencing (TnSeq) is a powerful approach for disc...
Transposon mutagenesis coupled to next-generation sequencing (TnSeq) is a powerful approach for disc...
Summary: Randomly barcoded transposon mutant libraries are powerful tools for studying gene function...
UnlabelledTransposon mutagenesis with next-generation sequencing (TnSeq) is a powerful approach to a...
UnlabelledTransposon mutagenesis with next-generation sequencing (TnSeq) is a powerful approach to a...
Random transposon mutagenesis allows for relatively rapid, genome-wide surveys to detect genes invol...
<p>A. A Mtb mutant library is created by phage-delivery of transposons, disrupting each genome with ...
Comprehensive mutant libraries can be readily constructed by transposon mutagenesis. To systematical...
Random transposon mutagenesis allows for relatively rapid, genome-wide surveys to detect genes invol...
Comprehensive mutant libraries can be readily constructed by transposon mutagenesis. To systematical...
Transposons are invaluable biological tools for the genetic manipulation of microorganisms. ISY100 f...
Re-programming microorganisms to modify their existing functions and/or to bestow bacteria with enti...
Transposons are invaluable biological tools for the genetic manipulation of microorganisms. ISY100 f...
Transposons are invaluable biological tools for the genetic manipulation of microorganisms. ISY100 f...
This work was supported by a Longer and Larger (LoLa) grant from the Biotechnology and Biological Sc...