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Meta/+Viromics.
Dead Sea, Archaeal viruses, Linux and all things fringe in microbiology!
Gophna lab
Dear #RNA_Virologists! I'm looking for community input on virus reporting standards - Please RT and check out the attached questionnaire and help me get educated! https://t.co/rAcSuiOysI
ps it's for my info slide
#RdRp_Summit
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RNA Virologists Survey - Good E-laboratory standards

Looking for feedback - the more informed we are about what the community wants, the better we can devise standards for minimal reporting, classification, and overall research standards.

Google Docs
Anyone have any recommendations for a webpage format/template for bioinformatics tutorials? Thinking about formalizing some I have on GitHub.
A super cool preprint is trending now (at least on twitter). The github repo link is 404 and AFAIK all new genome accessions/sequences are listed as 'pending'.
Not trying to shame the authors, but get the community's opinion on this:
Do you think it's OK to post and promote a preprint when the code/data/accessions are not publicly accessible?
Yes
0%
No
100%
Poll ended at .
You can move, but you can't hide: identification of mobile genetic elements with geNomad http://biorxiv.org/cgi/content/short/2023.03.05.531206v1?rss=1

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

Assembling the perfect bacterial genome using Oxford Nanopore and Illumina sequencing

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).

Unlike dsDNA phages that encode multiple proteins for active destruction of the target bacteria cell, the comparatively tiny 3-4 kb genomes of (ssRNA) Fiersviridae phages use a single, non-catalytic protein for cell lysis (also known as single gene lysis or Sgl systems).

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

#phage #viruses

Unpopular/way-too-niche opinion:
texlive packages are unnecessarily fragmented, and there is no reason each and every single one of those should have it's own documentation package.
Yes they may be tiny but doing a system update shouldn't mean 1/4 of the packages are texlive (which I only need as texlive is a dependency of some R packages I don't use) protip - if you're brave and on tumbleweed use regex to lock/taboo all texlive-*-doc
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--> http://rdrp.io/registration <--
In-person places are limited. Once filled, we can only accept virtual registrants so act fast!
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