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Floris Barthel Profile
Floris Barthel

@florisbarthel

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Assistant professor @TGen | Postdoc @jacksonlab @MDAndersonNews | Evolutionary cancer genomics | Glioma | Telomere dysfunction | Tweets are my own

Phoenix, AZ
Joined November 2009
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@florisbarthel
Floris Barthel
27 days
I had the opportunity to write an editorial for a piece in Neuro-Oncology (@NeuroOnc ) executing a genomic analysis on perhaps the largest cohort of extracranial metastases of adult gliomas to date.
academic.oup.com
Floris P Barthel; Uncommon Territory: The Clinical and Molecular Profile of Metastatic Gliomas, Neuro-Oncology, , noaf244, https://doi.org/10.1093/neuonc/n
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@florisbarthel
Floris Barthel
29 days
Why does the telomere interact with these distant repeats? We speculate that this is key for maintaining nuclear organization and may involve nuclear orphan receptors. Many questions remain. Read the paper to dive into the data 👇 #TelomereC #Genomics #Chromatin #Epigenetics
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@florisbarthel
Floris Barthel
29 days
We validated these contacts with classic 3C/PCR and confirmed the 3D proximity using Southern Blotting and stunning 3D FISH data, proving these are real, higher-order chromatin structures.
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@florisbarthel
Floris Barthel
29 days
Specifically, we found strong enrichment at three classes of repetitive elements: Interstitial Telomeric Sequences (ITS), Telomere-Associated Repeat 1 (TAR1), and D20S16 elements.
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@florisbarthel
Floris Barthel
29 days
The telomeric interactome spans the entire genome! While contacts are enriched near telomeres (<100 Kb), over 80% of all interactions occurred >5 Mb away from chromosome ends. This isn't just about the subtelomere.
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@florisbarthel
Floris Barthel
29 days
Our initial goal was to map telomeric regulation of key genes, like TERT. The reality? Gene-level interactions were massively outnumbered by contacts with repetitive elements! 🤯
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@florisbarthel
Floris Barthel
29 days
To map the telomeric interactome, we developed Telomere-C (Telomere Conformation Capture). This novel, ligation-free method uses a biotinylated PNA probe to capture telomeric DNA, allowing us to measure nuclear contacts efficiently using short-read sequencing.
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@florisbarthel
Floris Barthel
29 days
Excited to share our preprint (3rd of 2025) on the 3D telomeric interactome, a project that started with a K99 in 2018. Thanks to @YA_Chen_PhD, first postdoc in our lab and first author who worked tirelessly to realize this dream.
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biorxiv.org
Telomeres are essential for genome integrity, but the accurate, high-resolution mapping of their three-dimensional (3D) chromatin interactions, a process thought to mediate gene regulation and...
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@florisbarthel
Floris Barthel
1 month
Happy to get this one out at last. Might have to do a little thread on this later.
@biorxiv_genomic
bioRxiv Genomics
1 month
Mapping the Telomeric 3D Interactome with Telomere-C Reveals Repetitive Element Hubs Associated with Telomere Maintenance https://t.co/g0SD9YwSRn #biorxiv_genomic
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@florisbarthel
Floris Barthel
4 months
Massive credit to the brilliant PhD student @SharvariMankame, for leading this work. You can dive deeper into the science with our full thread on the other platform. #Glioblastoma #cfDNA #TGen #Research
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@florisbarthel
Floris Barthel
4 months
Excited to share our new preprint: "Cell-Free DNA Sequencing Uncovers the Longitudinal Consequences of Temozolomide Treatment and Host Co-Culture in Glioblastoma"! https://t.co/eyzixOEHoS
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biorxiv.org
Glioblastoma (GBM) is a highly aggressive brain tumor with limited options for longitudinal monitoring. We evaluated the potential of cell-free DNA (cfDNA) as a real-time biomarker of tumor burden...
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@florisbarthel
Floris Barthel
6 months
Two weeks ago we shared our lab's first manuscript on bioRxiv: https://t.co/53RIq5Fcm0 We performed diploid genome assembly to fully resolve the telomeres, centromeres and numerous other repeats of the BJ and IMR-90 fibroblast cell lines. Please get in touch with feedback!
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biorxiv.org
Human cell lines are fundamental tools in biomedical research and are widely used in disease modeling, drug development, and many other domains. Here, we present chromosome-level, phased diploid...
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@mpmeers
Michael Meers
10 months
I roughly calculated the state-level economic impact of withholding NIH grants in terms of jobs lost per day. For Missouri it's 79--553 jobs a week that this drags on. Data: https://t.co/PJyjsAcwWK How to contact your representatives with this information:
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usa.gov
Use USAGov’s Contact Your Elected Officials tool to get contact information for your members of Congress, the president, and state and local officials.
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@marianattestad
Maria Nattestad
1 year
Investigating structural variants? I just released a tutorial video showing how I do this quickly and intuitively using my tools Ribbon and SplitThreader: https://t.co/AlF0gR17kA
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@biorxiv_genomic
bioRxiv Genomics
1 year
A comprehensive survey of RNA modifications in a human transcriptome https://t.co/GepqiRyqUv #biorxiv_genomic
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@pashadag
PM @[email protected] @pashadag.bsky.social
1 year
In https://t.co/TpdlGQ2Nwv, @rayarayan, Yoann Dufresne and I comment on the decoupling of ‘population’ pangenome graphs from ‘application-specific’ pangenome graphs. (1/3)
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@DGautheret
Daniel Gautheret
1 year
Let me introduce Transipedia, our project for cancer RNA-seq exploration just published in Genome Biology, with @ChloeBessiere, @CamilleMrcht, @RayanChikhi, @hl_xue, M. Salson and Thérèse Commes’ lab in Montpellier. 1/9 👇 https://t.co/A8SmVgp8hG
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link.springer.com
Indexing techniques relying on k-mers have proven effective in searching for RNA sequences across thousands of RNA-seq libraries, but without enabling direct RNA quantification. We show here that...
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@nomad421
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1 year
Prestige signals and pedigree are anathema to the scientific endeavor and quite harmful to the community of scientists actively working to advance human knowledge.
@PracheeAC
Prachee Avasthi
1 year
Good job all the institutions claiming affiliation with the Nobel laureates. May all see you as part of the “because of” rather than “in spite of” narrative* *prestige signals are BS no matter who is using who
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