Lynn
1.2K posts

Lynn
@Lynn_evodevo
Postodoc @darwintreelife @sangerinstitute Working with @bat1kgenomes Affiliated @TrinCollCam|Previous postdoc @Chema_MD lab @QMUL|EvoDevo & Genomics Biologist
Cambridge, England Katılım Temmuz 2017
4.3K Takip Edilen403 Takipçiler
Lynn retweetledi

Thrilled to share our new paper in @emboreports, now online! We explored transcriptomic evolution during early embryogenesis of two spiralian annelids, to understand how early cell fate modes shape development before the gastrulation. #EvoDevo #Embryogenesis #RegulatoryEvolution
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Thrilled to attend my first SMBE annual meeting in Beijing at the end of July, I am honoured to present our work on Bat #Phylogenomics, and (unexpectedly) to be the last speaker of our session on the very last day.
Thanks to the organisers and everyone who joined! #Bat1K #Sanger




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I gave a 3-minute flash talk @sangerinstitute #ScienceDay last week, sharing my work with @bat1kgenomes consortium on bat phylogeny.
Grateful to the organisers and community!
So glad the open ending resonated with many in the genomics crowd!
#Phylogenomics #WomenInSTEM 🦇

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Truly honoured to have attended the EMBO #EvoDevoTempo workshop last month in Paris.
It was such a pleasure to present the works with @Chema_MD lab.
Grateful for the inspiring talks and the chance to connect with so many brilliant scientists.
#EvoDevo #AcademicLife #WomenInSTEM


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Lynn retweetledi

🚀 Our perspective is out in @Nature!
We present a roadmap for Multimodal Foundation Models (MFMs) — large AI models pretrained across multi-omics and multi-timepoint data — to serve as the computational backbone for building virtual cells.
Read the full paper in Nature: nature.com/articles/s4158…
🔍 Why MFMs?
Biology is inherently multimodal, and molecular layers are deeply interconnected and context-specific. MFMs aims to integrate these layers to uncover shared biological principles that govern diverse cell states, offering a unified substrate for downstream inference.
🧠 What’s new?
💡 From hypothesis-driven to data-centric workflows: MFMs shift biology’s paradigm. Instead of crafting bespoke models for narrow tasks, we can now pretrain over massive datasets, distill foundational knowledge, and refine insights through lab-in-the-loop experimentation—where models guide experiments, and experiments update models.
🧬 Conditional gene regulation: MFMs go beyond static models. By training across multiple omics layers (e.g., chromatin accessibility, transcriptomics), they can learn context-specific gene functions and regulatory programs—key to understanding development and disease.
🧪 In silico perturbation: Biology’s combinatorial complexity is immense—thousands of genes, millions of interactions. MFMs provide a framework to simulate perturbations before wet-lab execution. Trained on CRISPR perturb-seq data, they can predict molecular responses across cell types, tissues, and time—enabling programmable biology at scale.
⚙️ What makes MFMs possible?
Envisioned techniques include:
- Unified tokenization from nucleotides to pathways
- Hybrid attention across intra- and inter-modal interactions
- Prompt-driven multitasking for temporal prediction, conditional generation, and modality translation
- Human knowledge integration from curated databases and biomedical literature
These design principles translate the architecture of foundation models into the molecular domain.
⚠️ What are the challenges?
MFMs aren’t just about scale—they demand accessibility, reliability, and transparency.
- Low-resource learning techniques (e.g., LoRA, adapters) are vital for democratizing training
- Human-agnostic benchmarks are needed, as conventional labels may punish models that uncover novel biology
- Uncertainty modeling is essential to mitigate hallucinations and increase scientific trust
Interpretability and ethical stewardship must be foundational in this emerging ecosystem.
Kudos to all co-authors for the collective effort and vision: @HOATIANCUI1, @Alejandro__TL, @mariabrbic, @JulioSaezRod, @simocristea, @genophoria, @mo_lotfollahi, @fabian_theis.
Let’s build the future of virtual cells together.




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Happy New Year! 🎉 Excited to start 2025 by sharing our latest study from @Chema_MD lab! 🚨 #EvoDevo #EarlyEmbryogenesis
Cell fate specification modes shape transcriptome evolution in the highly conserved spiral cleavage biorxiv.org/content/10.110…
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In Memoriam: Professor Wen-Ying Yin (1922–2023) | Zootaxa mapress.com/zt/article/vie…
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Lynn retweetledi

BREAKING NEWS
The 2024 #NobelPrize in Physiology or Medicine has been awarded to Victor Ambros and Gary Ruvkun for the discovery of microRNA and its role in post-transcriptional gene regulation.

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Revisiting the four Hexapoda classes: Protura as the sister group to all other hexapods | PNAS pnas.org/doi/10.1073/pn…
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How we learned to build a gliding mammal thenode.biologists.com/how-we-learned… via @the_Node
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@Ella_Maru Yes, my current model is very speculative based on our results; many more explorations are needed in the future.
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@Lynn_Yan_Liang Thanks for the response, Lynn! It's definitely an interesting area to explore. Hopefully, new genetic tools will make it possible in the future.
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The paper from my first PhD project on “The functional evolution of collembolan Ubx on the regulation of abdominal appendage formation” is now online! #EvoDevo #Collembola
Read it here: link.springer.com/article/10.100…
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@Ella_Maru Thanks for your interest! It is a pity we cannot investigate the post translational regulation of Ubx “during late embryogenesis” due to the lack of genetic tools; but I agree it could be worthy to explore whether those regulation would alter Ubx’s function temporally.
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@Lynn_Yan_Liang Congratulations! Have you investigated post-transcriptional regulation of Ubx and Dll during late embryogenesis?
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