Tue Sparholt Jørgensen
@tuesparholt.bsky.social
300 followers 89 following 29 posts
Posts Media Videos Starter Packs
Pinned
tuesparholt.bsky.social
Bacterial telomeres are common, just not so much in RefSeq 'complete' genomes. But they can be added by the new tool David Faurdal wrote. I am thrilled to see this out as a preprint here: www.biorxiv.org/content/10.1... @tilmweber.bsky.social @thombooth.bsky.social
Reposted by Tue Sparholt Jørgensen
stephenturner.us
From genotype to phenotype with 1,086 near telomere-to-telomere yeast genomes www.nature.com/articles/s41... 🧬🖥️🧪 github.com/HaploTeam/10...
Reposted by Tue Sparholt Jørgensen
stcmicrobeblog.bsky.social
𝘚𝘵𝘳𝘦𝘱𝘵𝘰𝘮𝘺𝘤𝘦𝘴 (and 𝘒𝘪𝘵𝘢𝘴𝘢𝘵𝘰𝘴𝘱𝘰𝘳𝘢🙂) aficionadas y aficionados take note 👇

...and no, the image doesn't show reconstituted 𝘒𝘪𝘵𝘢𝘴𝘢𝘵𝘰𝘴𝘱𝘰𝘳𝘢 telomeres (telomores) 😉
#MicroSky
image from https://alchetron.com/Kitasatospora
tuesparholt.bsky.social
this project has been such a joy, and collaborating with dalofa.bsky.social, @thombooth.bsky.social and @tilmweber.bsky.social had been fantastic, it has been everything I ever dreamed an academic collaboration could be. Thank you guys!
tuesparholt.bsky.social
...an information which David then used to beautifully show that the protein folds similarly in structure but not in sequence to the known telomere maintenance systems main DNAbinding domain.
tuesparholt.bsky.social
Then @thombooth.bsky.social used the presence/absence of known telomere proteins to identify a potentially new telomere protein which is linked to the Sg2247 class telomere, which previously did not have an identified maintenance system (notice the dot in the red circle)
tuesparholt.bsky.social
David then analyzed the end replication proteins and could identify a known system in 76% of strains. Extremely interestingly, he used that to show that certain telomere sequences are linked to specific telomere maintenance proteins.
tuesparholt.bsky.social
To our knowledge, the >2000 telomeres which were clustered into 137 groups is the first large scale attempt at dissecting the diversity of the telomeres of streptomyces, and allow us to make additional discoveries, like the potentially #plasmid specific AGA telomere.
tuesparholt.bsky.social
We noticed that quite few of the RefSeq genomes had replicon ends which clustered as telomeres, and decided to quantify it: while only 15% of RefSeq 'complete' chromosomes were found to have both telomeres, 78% of Telomore completed chromosomes had both telomeres.
tuesparholt.bsky.social
After figuring out how to attach the missing telomeres, we went on to extract replicon ends from #RefSeq to make a compendium of >2000 streptomycetaceae telomeres, clustered by sequence similarity into 137 groups with 4-300+ members.
tuesparholt.bsky.social
The tool, Telomore, works by mapping first long then short reads to linear replicon ends, then building a consensus sequence from the reads overhanging the end, then attaching the consensus to create a complete sequence with no gaps.
tuesparholt.bsky.social
Bacterial telomeres are common, just not so much in RefSeq 'complete' genomes. But they can be added by the new tool David Faurdal wrote. I am thrilled to see this out as a preprint here: www.biorxiv.org/content/10.1... @tilmweber.bsky.social @thombooth.bsky.social
Reposted by Tue Sparholt Jørgensen
jamesbriscoe.bsky.social
The @crick.ac.uk is recruiting Early Career Group Leaders

- Lab set-up, research costs, salaries for up to 5 researchers
- Support for up to 12 years
- Access to our core facilities
- Competitive salary
- Fantastic colleagues
- All areas of biology

Deadline 27 Nov

www.crick.ac.uk/careers-stud...
Early career group leaders
We appoint researchers from across biology and biomedicine to set up their first groups at the Crick.
www.crick.ac.uk
Reposted by Tue Sparholt Jørgensen
oschwengers.bsky.social
Dear community, Bakta needs your help!

To further improve the functional annotation of "hypothetical" CDS, me and @gbouras13.bsky.social, we are looking for the worst Bakta-annotated bacterial genomes ;-)

(1/2)
Reposted by Tue Sparholt Jørgensen
johninnescentre.bsky.social
VACANCY - Independent research fellowships leading to tenured positions

We’re inviting applications from outstanding researchers who either hold, or wish to apply for, Independent Research Fellowships.

APPLICATION DEADLINE: 10 November 2025

Click here to apply: jic.link/Fellows
Reposted by Tue Sparholt Jørgensen
kleinman.bsky.social
RIP Jane Goodall, by all accounts a wonderful woman who loved this Far Side cartoon
Reposted by Tue Sparholt Jørgensen
zaminiqbal.bsky.social
Delighted to see our paper studying the evolution of plasmids over the last 100 years, now out! Years of work by Adrian Cazares, also Nick Thomson @sangerinstitute.bsky.social - this version much improved over the preprint. Final version should be open access, apols.
Thread 1/n
tuesparholt.bsky.social
This tool looks incredible, I've been missing something exactly like this to analyze assembly graphs, which is necessary to understand more complex genome structures.
Reposted by Tue Sparholt Jørgensen
New blog post – A quick look at Roche's SBX
lh3.github.io/2025/09/11/a...
Reposted by Tue Sparholt Jørgensen
jimshaw.bsky.social
Preprint out for myloasm, our new nanopore / HiFi metagenome assembler!

Nanopore's getting accurate, but

1. Can this lead to better metagenome assemblies?
2. How, algorithmically, to leverage them?

with co-author Max Marin @mgmarin.bsky.social, supervised by Heng Li @lh3lh3.bsky.social

1 / N
biorxiv-bioinfo.bsky.social
High-resolution metagenome assembly for modern long reads with myloasm https://www.biorxiv.org/content/10.1101/2025.09.05.674543v1
tuesparholt.bsky.social
It's wild how different the illumina error % is between the two plots, at 15 nt homopolymer one shows 2% error and the other 20% error (phred 7 vs ca 17). Or am I missing something? bsky.app/profile/albe...
albertvilella.bsky.social
Illumina publishes a new "HP homopolymer Advanced Recipe" for the NextSeq 2000 instrument line.
Reposted by Tue Sparholt Jørgensen
aphillippy.bsky.social
Definitely hard to measure, but here is our best attempt from a new benchmarking paper to be preprinted in the next few weeks. Element appears to be the current king of homopolymers. Illumina does worse than HiFi beyond 20 bp. (This is all measured on human DNA)
tuesparholt.bsky.social
True, I think six PCR cycles inside the instrument? might be different on different instruments. But PCR free libprep is still better for high and low GC regions. I randomly saw this yesterday which seems to indicate the error % for 20+ homopolymers, it might not cover 60nt bsky.app/profile/albe...
albertvilella.bsky.social
Illumina publishes a new "HP homopolymer Advanced Recipe" for the NextSeq 2000 instrument line.
tuesparholt.bsky.social
Thank you for the answer! Did you map the nanopore reads back to the fixed sequence to see if your nanopore data had captured them and they didn't assemble or if they were absent from the data? How long are the telomeres? I wonder why other nanopore read sets could assemble telomeres