International audienceThe generation of a large collection of defined transposon insertion mutants is of general interest to the Caenorhabditis elegans research community and has been supported by the European Union. We describe here a semi-automated high-throughput method for mutant production and screening, using the heterologous transposon Mos1. The procedure allows routine culture of several thousand independent nematode strains in parallel for multiple generations before stereotyped molecular analyses. Using this method, we have already generated >17 500 individual strains carrying Mos1 insertions. It could be easily adapted to forward and reverse genetic screens and may influence researchers faced with making a choice of model organis...
The nematode Caenorhabditis elegans has been used to study genetics and development since the mid-19...
Caenorhabditis elegans has a complete annotated genome sequence that is augmented by increasing quan...
Whole-genome sequencing (WGS) is becoming a fast and cost-effective method to pinpoint molecular les...
International audienceThe generation of a large collection of defined transposon insertion mutants i...
Methods that use homologous recombination to engineer the genome of C. elegans commonly use strains ...
International audienceMethods that use homologous recombination to engineer the genome of C. elegans...
<div><p>Methods that use homologous recombination to engineer the genome of <em>C. elegans</em> comm...
Methods that use homologous recombination to engineer the genome of C. elegans commonly use strains ...
We have generated a recombinant Mos1 transposon that can insert up to 45-kb transgenes into the Caen...
Reverse genetic or gene-driven knockout approaches have contributed significantly to the success of ...
Background: The original sequencing and annotation of the Caenorhabditis elegans genome along with r...
We have generated a recombinant Mos1 transposon that can insert up to 45 kb transgenes into the C. e...
semi-automated high-throughput approach to the generation of transposon insertion mutants i
Many investigators have being using CRISPR-Cas9 as a method of genome engineering because it is easy...
Eukaryotic genomes are replete with transposable elements. The nematode C. elegans will be the first...
The nematode Caenorhabditis elegans has been used to study genetics and development since the mid-19...
Caenorhabditis elegans has a complete annotated genome sequence that is augmented by increasing quan...
Whole-genome sequencing (WGS) is becoming a fast and cost-effective method to pinpoint molecular les...
International audienceThe generation of a large collection of defined transposon insertion mutants i...
Methods that use homologous recombination to engineer the genome of C. elegans commonly use strains ...
International audienceMethods that use homologous recombination to engineer the genome of C. elegans...
<div><p>Methods that use homologous recombination to engineer the genome of <em>C. elegans</em> comm...
Methods that use homologous recombination to engineer the genome of C. elegans commonly use strains ...
We have generated a recombinant Mos1 transposon that can insert up to 45-kb transgenes into the Caen...
Reverse genetic or gene-driven knockout approaches have contributed significantly to the success of ...
Background: The original sequencing and annotation of the Caenorhabditis elegans genome along with r...
We have generated a recombinant Mos1 transposon that can insert up to 45 kb transgenes into the C. e...
semi-automated high-throughput approach to the generation of transposon insertion mutants i
Many investigators have being using CRISPR-Cas9 as a method of genome engineering because it is easy...
Eukaryotic genomes are replete with transposable elements. The nematode C. elegans will be the first...
The nematode Caenorhabditis elegans has been used to study genetics and development since the mid-19...
Caenorhabditis elegans has a complete annotated genome sequence that is augmented by increasing quan...
Whole-genome sequencing (WGS) is becoming a fast and cost-effective method to pinpoint molecular les...