Brunet Lab
@BrunetLab
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Aging lab @Stanford - Epigenomics and metabolism in #aging; Brain aging and rejuvenation; Neural stem cells; C. elegans; African #killifish
Stanford, CA
Joined March 2010
My group at Calico is looking for a summer intern. We develop machine learning methods to understand gene regulation—how sequence determines expression, how variants alter function, and what human genetics can tell us about aging.
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New work describes our efforts to achieve CRISPR editing of the mitochondrial genome. https://t.co/L98rtFj5Yq The CRISPR toolbox has revolutionized the study of nuclear DNA, but the mitochondrial genome (mtDNA) has remained out of reach, mainly because there are no known ways
biorxiv.org
Mitochondria, which evolved from symbiotic bacteria, possess their own genomes (mtDNA) and support independent transcription and translation within the organelle. Given the essential role of mtDNA in...
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Can we predict the spatial effects of single-cell perturbations? Excited to share our preprint introducing SpatialProp, which computationally propagates single-cell transcriptomic perturbations across tissues, along with key frameworks for evaluating spatial perturbation models.
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Congrats to @juliaschaepe and @marklundem on the recent publication of their work linking the binding behaviors of TFs in vitro and in vivo! Out in Cell now:
cell.com
In vitro-derived insights into features that drive transcription factor binding to DNA, including motif-adjacent sequence, enable prediction of chromatin states and transcription factor occupancy in...
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⏰ Deadline Nov 20 (11:59pm MST)! Submit short talk abstracts & scholarship applications for the Keystone Symposium on Aging and share the stage with top researchers in aging, immunity & inflammaging. 📝 https://t.co/XvrgfYVMuJ
@BrunetLab #KSAging26 #aging #inflammaging
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Exciting neurogenesis meeting in the Swiss Alps!! 'Neurogenesis from development to adulthood in health and disease' To submit an application: asconameeting@unige.ch
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Congratulations @EricDSun!! Well deserved!!
Exciting news! We're thrilled to announce the six outstanding laureates of the International Birnstiel Award for Doctoral Studies in Molecular Life Sciences 2025! 🏆Congratulations to all awardees and honourable mentions! 🎉 1/ ➡️ https://t.co/yyFVrN93V5
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Very happy to share the most recent work from the lab!
1/ 🧵Happy to share our preprint from @WJGreenleaf’s Lab: beCasKAS, our method to directly detect #CRISPR base editor off-targets in primary cells. We additionally show how non-coding edits can be triaged for epigenetic dysregulation using deep learning. https://t.co/i7eHqKXrje
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Excited to share our work with @DMSabatini & @JswLab. How do lysosomes change with age? We present a metabolic atlas of lysosomal aging, and reveal a lysosomal “aging clock” of metabolites linked to lysosomal storage disorders. Grateful to all co-authors! https://t.co/HyP6zq3Ccq
biorxiv.org
Lysosomal dysfunction is a well-recognized feature of aging, yet its systematic molecular investigation remains limited. Here, we employ a suite of tools for rapid lysosomal isolation to construct a...
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We are excited to share our latest work in @ScienceMagazine studying cooperative behavior in both biological and artificial intelligence systems — fantastic work by @JanineJiang22, Linfan Gu, and wonderful collaboration with @JonathanCKao! https://t.co/nVxe3E3fGA
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Today, we report Germinal, a method for efficient de novo antibody design, with @santimillef and @SynBioGaoLab. Germinal achieves success rates of 4-22% across diverse epitopes. We make the work fully open, without doing lame things like posting a preprint without methods. 🧵
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Interested in aging and longevity? Very exciting Keystone meeting in March 2026 on immune function, organ health, and aging! (organized with Eric Verdin, Manuel Serrano, and Eline Slagboom) Check it out!! https://t.co/PKR8DchIkZ
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Welcome to the age of generative genome design! In 1977, Sanger et al. sequenced the first genome—of phage ΦX174. Today, led by @samuelhking, we report the first AI-generated genomes. Using ΦX174 as a template, we made novel, high-fitness phages with genome language models. 🧵
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Can you rejuvenate an old brain by giving it young immune cells? 🧠 My lab @calico put it to the test. In our new study, we replaced the brain's immune cells in old mice with young ones. The result? The old brain environment forced the young cells to age RAPIDLY. A 🧵👇
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Our spatiotemporal atlas of brain aging under caloric restriction is out: https://t.co/15iBbqGLuX. Thanks to all authors, reviewers, and the great support from @RockefellerUniv, Brain Research Foundation (@TheBRF), and the Center for Integrated Cellular Analysis (@cegs_ica)!
Excited to share our first anti-aging intervention study, led by brilliant Zehao @Tommyz626, Alex @alexepstein_bio, and Chloe @chloe__schaefer from our lab at @RockefellerUniv! With a cost-effective spatiotemporal analysis pipeline, we identified the aging-associated cell
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New exciting work from Jae Ho Lee in our lab, in a fantastic collaboration with Alessandro Ori @AOri_lab and Alessandro Cellerino @Alessan82703458 on why and how the brain ages and becomes vulnerable to neurodegenerative diseases
science.org
Aging is a major risk factor for neurodegeneration and is characterized by diverse cellular and molecular hallmarks. To understand the origin of these hallmarks, we studied the effects of aging on...
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⚡️Thrilled that #VirtualLab is published in @Nature! https://t.co/BwAsLFAeua We created a team of AI agents to mirror my Stanford lab🤖. Led by a PI agent, the AI scientists ran their own group meetings and discovered effective binders to new CoVID variants that we validated.
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I'm excited to share work on a research direction my team has been advancing: connecting machine learning derived genetic variant embeddings to downstream tasks in human genetics. This work was led by the amazing @divyanshi91!
biorxiv.org
Genome-wide association studies (GWAS) have identified thousands of trait-associated loci. Prioritizing causal variants within these loci is critical for characterizing trait biology. Statistical...
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