Gregor Diensthuber
@gdiensthuber.bsky.social
120 followers 220 following 25 posts
PhD student @NovoaLab @CRGenomica |Wet-Lab 🔁 Dry-Lab | RNA modifications | Method Development 🧬⚒
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Reposted by Gregor Diensthuber
ferriol.bsky.social
Very excited to share our new paper on the influence of biological sex and smoking in the clonal landscape of normal human bladder, just published in Nature.
A big thank you and congrats to all the authors, specially to @raquelbmi.bsky.social for all the shared efforts in this journey!

⬇️More info⬇️
Reposted by Gregor Diensthuber
novoalab.bsky.social
Novoa Lab joined the PRBB Open Day 2025🔬🧬🌊 @prbb.org to share our passion for RNA research with the public. Thanks to everyone who came to explore science with us and thanks organisers for making this event possible! #PRBBOpenDay #OpenScience
Reposted by Gregor Diensthuber
tanentzapflab.bsky.social
The goal of a PhD is not to learn some facts or read a few papers or learn a bunch of techniques. The goal of a PhD is to learn independence, problem solving, how to finish things you start, resilience, & gain the ability to adapt & think creatively. Learning these things is hard.
Reposted by Gregor Diensthuber
paveltomancak.bsky.social
Looks like private funders, HHMI,CZI etc., are not going to “save” US research. Europe is setting up mechanisms to attract US researchers & it may work. But, common, target junior talent, don’t shower money on superstars who will be flying professors & return to US when the science winter passes.
Reposted by Gregor Diensthuber
raflynn5.bsky.social
RNA N-glycosylation enables immune evasion and homeostatic efferocytosis by chemically caging acp3U. Excited to report this work lead by Vinnie @vinnieviruses.bsky.social and in collaboration with @vijayrathinam.bsky.social in @nature.com www.nature.com/articles/s41...
Reposted by Gregor Diensthuber
jsantoyo.bsky.social
Systematic benchmarking of basecalling models for RNA modification detection with highly-multiplexed nanopore sequencing. #DirectRNAsequencing #DRS #RNAmodifications #Nanopore #Genomics #Bioinformatics #ModelBenchmarking #Basecalling @biorxivpreprint.bsky.social
www.biorxiv.org/content/10.1...
gdiensthuber.bsky.social
Moreover, for m1Y and Y, I am not aware of a non-enzymatic reaction that could convert one into the other during any downstream processing (leading to contamination). Unlike for m1A which can be converted to m6A at high temperatures, something that could happen easily at a heat inactivation step.
gdiensthuber.bsky.social
Hi James,
thanks for the nice words! I am speculating here but I think it is the latter. The training data should be synthetic sequences containing each of the modifications, and therefore quite clean.
gdiensthuber.bsky.social
Huge thanks to all the incredible people @novoalab.bsky.social that helped make this work possible! #rnasky #nanopore
gdiensthuber.bsky.social
Finally, we established that a combination of alignment and current features still presents a robust way of detecting RNA modifications with RNA004, as demonstrated on E.coli strains knockout for certain mod writers. (11/12)
gdiensthuber.bsky.social
While IVTs helped remove sequence-specific FPs two classes of FPs remained: I) cross-reactive mods found on the same base, and II) mods at adjacent positions (+/- 1nt) from identified FP sites, which cannot be accounted for with existing methods. (10/12)
gdiensthuber.bsky.social
Considering the substantial amount of FPs observed at unannotated sites we reasoned that the use of IVT controls might be necessary to help remove sequence specific FPs. (9/12)
gdiensthuber.bsky.social
From there we moved to rRNAs for benchmarking since accurate mod. maps exist for well-studied species. We could recapitulate most Ψ and m5C sites while also observing substantial FP, especially at base methylations and unannotated sites. (8/12)
gdiensthuber.bsky.social
Moving to per-site predictions (removing per read estimates that fall below the default cutoff), we observe that most models slightly underpredict the per-site stoichiometries with the pseU model performing the most accurate (particularly in the 0-25% modified range). (7/12)
gdiensthuber.bsky.social
Digging a bit deeper, we can identify particular sets of sequences (5mer) that produce lower probability estimates than the remaining ones, suggesting a strong impact of the sequence context on predictions. (6/12)
gdiensthuber.bsky.social
Key observations (per-read): 1) in general, models perform well. 2) Ψ and m1Ψ are indistinguishable. 3) m5C and hm5C cross-react in particular sequence contexts as indicated by the bimodal distribution of hm5C called with the m5C model. (5/12)
gdiensthuber.bsky.social
But first, a quick word on mod-aware basecallers and the information they provide. The models make predictions on a per-read and position basis (per-read) which can then be collapsed into per-site predictions, using downstream tools which consider a certain filter-threshold (per-site).
gdiensthuber.bsky.social
Next we went ahead and sequenced synthetic oligos containing all possible 5mers (n=1024) to assess model performance, cross-reactivities and potential sequence biases. (3/12)
gdiensthuber.bsky.social
First things first, we updated SeqTagger to support 96 barcodes with the newest sequencing chemistry (RNA004). If you are interested in multiplexing your own DRS runs the new model is openly available here -> github.com/novoalab/Seq.... Feedback is very welcome! (2/12)
Reposted by Gregor Diensthuber
novoalab.bsky.social
Another epic Novoa Lab retreat in the books!
A big thank you to everyone who made it such a success — from the science-packed discussions and hands-on workshops to the brainstorming, games, sunny pool sessions, and delicious BBQs. And special thanks to the organizers!⚘️
@evamarianovoa.bsky.social
gdiensthuber.bsky.social
Hätte mir vom Standard ein höheres Niveau erwartet, aber Klicks sind Klicks nehme ich an.
Reposted by Gregor Diensthuber
crg.eu
Endinsa’t en una vivència sensorial única que connecta ciència i art immersiu. “SEEING: Un ull i una caixa” arriba del 5 al 14 de juny al Centre Cívic Convent de Sant Agustí (Carrer del Comerç 36, Barcelona). www.crg.eu/en/event/see...