ps it's for my info slide
#RdRp_Summit
😉
You can move, but you can’t hide: identification of mobile genetic elements with geNomad
https://www.biorxiv.org/content/10.1101/2023.03.05.531206v1
Killer software for phage, prophage, and plasmid discovery, available at:
https://portal.nersc.gov/genomad/
Our (me, Louise Judd and @DrKatHolt) new paper was recently published in @PLOSCompBiol:
https://doi.org/10.1371/journal.pcbi.1010905
I'm particularly fond of this one, as it takes my PhD thesis and distils it down to practical advice.
There's also an accompanying tutorial with sample data where you can try the assembly method for yourself:
https://github.com/rrwick/Perfect-bacterial-genome-tutorial/wiki
A perfect bacterial genome assembly is one where the assembled sequence is an exact match for the organism’s genome—each replicon sequence is complete and contains no errors. While this has been difficult to achieve in the past, improvements in long-read sequencing, assemblers, and polishers have brought perfect assemblies within reach. Here, we describe our recommended approach for assembling a bacterial genome to perfection using a combination of Oxford Nanopore Technologies long reads and Illumina short reads: Trycycler long-read assembly, Medaka long-read polishing, Polypolish short-read polishing, followed by other short-read polishing tools and manual curation. We also discuss potential pitfalls one might encounter when assembling challenging genomes, and we provide an online tutorial with sample data (github.com/rrwick/perfect-bacterial-genome-tutorial).
Intriguing manuscript looking into the range of viruses that form a phage nucleus during infection. Amazing bioinformatics and experimental work, and beautiful figures!
Identifying the core genome of the nucleus-forming bacteriophage family and characterization of Erwinia phage RAY
https://www.biorxiv.org/content/10.1101/2023.02.24.529968v1?rss=1