The command-line tool MGEfinder identifies large insertions and genotypes them with respect to a reference genome.
It is designed to work with haploid genomes, and has been tested extensively on bacteria.
It can identify mobile genetic elements and their sites of insertion using an ab initio approach.
Follow the links below to learn more.
We have added a new feature in MGEfinder v1.0.5 that allows you to run an MGEfinder workflow without isolate assemblies. This means that you no longer need to assemble each isolate if you already know what elements you are looking for. You just need a working directory that includes this file:
myWorkdir/00.database/database.fna
Instead of the myWorkdir/00.assembly
directory. The 00.database/database.fna
file is a FASTA file of the elements that you are searching for. For example, if you just want to look at IS6110 insertions in M. tuberculosis, you can place a copy of that IS element in the 00.database/database.fna
file. You can then run the workflow with the command
mgefinder workflow database myWorkdir
While the original de novo workflow that requires assemblies can be run with:
mgefinder workflow denovo myWorkdir
Let me know if you have questions, and I hope you find it useful!
This is a flag you can add to the mgefinder workflow
commands to potentially increase sensitivity. These settings have not been validated, but they should make it easier to identify certain integrative mobile element insertions, in particular insertions that create a direct repeat between 20 bp and 50 bp in length. This should help to increase sensitivity to detect insertions of elements that insert via a tRNA-targeting tyrosine integrase, for example.
You can use it with
mgefinder workflow database --sensitive myWorkdir
or
mgefinder workflow denovo --sensitive myWorkdir
Let me know if you have any questions by submitting an issues.
While MGEfinder can detect a wide variety of site-specific integrative mobile elements, it is best suited for transposable elements. For example, certain types of tRNA-targeting mobile elements will be missed by MGEfinder by default because of their unique integration mechanism, whereby they replace the target sequence with a new sequence to repair the tRNA. But MGEfinder can still find these integrative elements if you adjust the parameters properly. If you use the --sensitive
flag when running mgefinder workflow denovo
or mgefinder workflow database
, you should be able to better detect these elements. If you would like more advice on how to do this, please open an issue with your request.
Durrant, M. G., Li, M. M., Siranosian, B. A., Montgomery, S. B. & Bhatt, A. S. A Bioinformatic Analysis of Integrative Mobile Genetic Elements Highlights Their Role in Bacterial Adaptation. Cell Host & Microbe 0, (2019)
Please also consider viewing my video presentation of this paper, provided through JRNLclub.
Please submit any questions or comments to our issues handler.