New publication!
How can you tell if a variant is pathogenic? We benchmarked several computational tools to predict the pathogenicity of autosomal dominant inherited retinal diseases. We identified the top-performing tools and found some new variants!
https://t.co/d5wEFmo2OX
From our physician-scientist development category:
https://t.co/xdyWDRISZC
Daniel C. Brock @DanielCBrock Cynthia Y. Tang @_CynthiaTang & team @A_P_S_A analyzed 36,298 applicants, reporting dual-degree training shapes residency application strategies, interview rates, specialty choice, and program prestige. Deborah Rupert @DoubleDocDDR, Toni Darville @darville_toni, Caroline Jansen @careyjans, Elias Wisdom @EliWisdom16
#MedicalEducation #ResidencyMatch #PhysicianScientists
We found a surprisingly large technical artifact hiding in a widely-used scRNA-seq technology.
In all Flex v1 datasets we’ve analyzed, we see hundreds of DE genes between probe set barcodes.
More on why this matters and what to do about it below:
https://t.co/BUdKnQ98lN
(1/n)
Check out this publication by our student @DanielCBrock Dual‑Degree Pathways in the Residency Match: A Comparative Analysis of Application Behaviors and Outcomes - PubMed https://t.co/OJQeTJtBci
Inspired by @JswLab, we generated a mini Genome-wide Perturb-seq, using just two 10x lanes (!).
Far too much data for one tweet (or one Figure), but it works beautifully.
The ability to assess the molecular function of every gene in an afternoon is mind-boggling
1/ You're not just sequencing single cells.
You're sequencing the soup they're in.
Ambient RNA is everywhere in single-cell RNA-seq. Here's how to fix it.
DNA methylation goes spatial! Introducing Spatial-DMT: a technology that co-profiles DNA methylation and transcriptome in the same tissue section. A fantastic collaboration with @zhouwanding lab. Kudos to Chin Nien Lee @ChinNLee2021 and Hongxiang Fu! https://t.co/895gPK9lKr
Drop by poster B0008 today to learn about genetic risk factors for retinal detachment! We found that variants in VSX2 were associated with an increased risk of retinal detachment in the UK Biobank.
Shout out to my PIs Ben Frankfort and Ryan Dhindsa!
@ARVOinfo#visionscience
Today at the #JointMeeting2025, Svetlana Mojsov, 2024 #LaskerLaureate, gave an impressive overview of how her research on GLP-1 revolutionized the field of glucose metabolism. Her findings led to development of novel therapeutics for #diabetes and #obesity. @A_P_S_A
🚀 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: https://t.co/VCWFeNDgUD
🔍 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.
Amazing @A_P_S_A South Regional Meeting this year! It was a treat talking to undergrads about the work we do @BCM_MSTP@BCMFromtheLabs and providing mentorship/guidance on their next steps as future physician scientists. And huge shoutout to our amazing chair @DanielCBrock!
Check out our two new papers with new single-cell tech/methods/data!
1. Phospho-seq: Multi-modal profiling of intracellualar proteins
https://t.co/6z5rx0UeNU
2. Systematic Perturb-seq of signaling regulators (2.6M cells, 6 cell lines, 1500 perturbations)
https://t.co/PPc31sW0dO
Thrilled the APSA South Regional Meeting was a success! 🎉
Huge thanks to attendees, organizers, @BCM_MSTP & @TexasChildrens hosting, and @A_P_S_A for making it happen!
Interested in hosting next year’s meeting? DM me—we’ve got resources to share! #APSA#PhysicianScientists