Jonas Fuchs

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Jonas Fuchs

Jonas Fuchs

@_JonasFuchs

Fascinated about virus evolution. Working on SARS-CoV-2. PostDoc at the Institute of Virology @Uniklinik_Fr

Freiburg Germany Katılım Kasım 2021
92 Takip Edilen79 Takipçiler
Jonas Fuchs
Jonas Fuchs@_JonasFuchs·
New preprint is out! Go check it out: varVAMP: automated pan-specific primer design for tiled full genome sequencing and qPCR of highly diverse viral pathogens Thanks to all the super cool people involved in this project :). biorxiv.org/content/10.110…
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Jonas Fuchs
Jonas Fuchs@_JonasFuchs·
We just released a major update for varVAMP allowing the design of PCR primers on highly variable alignments. Now it finds more primers, allows to predict off-targets with a BLAST db and more. Go check it out. Credits go to Wolfgang Maier @galaxyproject github.com/jonas-fuchs/va…
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Simona Cristea
Simona Cristea@simocristea·
MEGA-CRISPR (multiplexed effector guide arrays) is an alternative to CRISPR editing that edits RNA instead of DNA. It swaps the DNA-cutting enzyme Cas9 for an RNA-cutting alternative called Cas13d. As mRNA doesn’t last very long in a cell, any potential mistakes disappear fast. MEGA-CRISPR can shut down the production of multiple proteins, turning off up to 10 genes at once. To showcase the power of this system, a new paper addressed a really important clinical problem: T cell exhaustion in immunotherapy treatment for cancer patients. What this means is that, when either natural or engineered T cells (such as in CAR-T therapy) are chronically activated too many times by a tumor for example, they lose their effectiveness and ultimately stop reacting. The paper tunes exhaustion markers using an antibiotic switch of varying dose, creating a system that can essentially react dynamically and turn genes on/off as a function of a varying input. This system is an important advance because (1) editing mRNA is more versatile & less consequential than editing DNA (2) it can edit very many genes at a time (up to 10) (3) it can tune these many genes on/off using an external input Exciting times ahead for cell therapies in oncology! nature.com/articles/d4158…
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Martin Hölzer
Martin Hölzer@martinhoelzer·
We find DNA/RNA contamination in seq data, seq collections, & asssemblies. Either from biological sources, spike-ins, unwanted targets. We provide an easy-to-use @nextflowio pipeline for reference- and mapping-based decontamination, latest release: github.com/rki-mf1/clean/…
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Johannes Köster (@johanneskoester.bsky.social)
I am happy to finally announce the release of #Snakemake 8.0! In about half a year, we have modernized large parts of the code base. Most importantly, Snakemake 8.0 introduces a versatile plugin system, redesigned support for external storage, and modernized documentation. (1/n)
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Jonas Fuchs
Jonas Fuchs@_JonasFuchs·
Just updated virHEAT (github.com/jonas-fuchs/vi…) to version 0.6 (conda and pip). Let's you visualize microbial evolution at the snp level as a heatmap. Now you can restrict the plot to specific genomic regions with --zoom. SARS-COV-2 example: #SARSCoV2 #Bioinformatics
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Hugh Kearns
Hugh Kearns@ithinkwellHugh·
Really scary!!
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Jonas Fuchs
Jonas Fuchs@_JonasFuchs·
@Flahless1 We have done designs for quite a few viruses but not for noroviruses so far. If you want I can give it a go or walk you through it! Just drop me a mail.
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Jonas Fuchs
Jonas Fuchs@_JonasFuchs·
Just updated varVAMP to version 0.9.4. Designed for pan-specific primer design for full viral genome sequencing: github.com/jonas-fuchs/va…. Now used to design a novel pan-lineage primer scheme for SARS-CoV-2. Thx to @martinhoelzer for providing the alignment. In silico, not tested!
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Jonas Fuchs
Jonas Fuchs@_JonasFuchs·
@cinnetcrash1 The only thing varVAMP needs is an alignment. So an alignment of a variable bacterial gene is just fine. I have tested it up to 200 kb, but then it runs a bit due to the complexity of the graph that is used to find the best scheme. So go for it! If you need help let me kow!
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Gültekin Ünal
Gültekin Ünal@cinnetcrash1·
@_JonasFuchs This is looking cool. I wonder if this tool is only for viral pathogens? Can we use this for bacteria for specific genes as well?
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Ryan Hisner
Ryan Hisner@LongDesertTrain·
Really happy to see our paper on SARS-CoV-2 evolution in the Omicron era out in @Nature Microbiology today. I'd normally write a thread outlining our paper, but I've not felt well for a while & can't focus well enough to do much of anything. Will try to write one later.
Eric Topol@EricTopol

How #SARSCoV2 is continuing to evolve in the Omicron era, by many of the guiding lights who have so diligently tracked this virus throughout the pandemic nature.com/articles/s4156… @NatureMicrobiol by @CorneliusRoemer @PeacockFlu @DannySheward @LongDesertTrain @siamosolocani

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Jonas Fuchs
Jonas Fuchs@_JonasFuchs·
Happy to have finalized this small project. github.com/jonas-fuchs/BA… Create interactive coverage plots from your mapped viral read and usefull tracks such as genbank files.
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