Matteo Di Bernardo (@mat10_d) profile picture

PhD student @MITCSBPhD with @iaincheeseman, previously @FulbrightPrgrm Nigeria, @columbiacancer

Cambridge, MA
Joined November 2013
Photo by Matteo Di Bernardo (@mat10_d)Photo by Matteo Di Bernardo (@mat10_d)Photo by Matteo Di Bernardo (@mat10_d)Photo by Matteo Di Bernardo (@mat10_d)Photo by Matteo Di Bernardo (@mat10_d)Photo by Matteo Di Bernardo (@mat10_d)Photo by Matteo Di Bernardo (@mat10_d)Photo by Matteo Di Bernardo (@mat10_d)Photo by Matteo Di Bernardo (@mat10_d)Photo by Matteo Di Bernardo (@mat10_d)
EVOLVEpro is now out in @ScienceMagazine! It was wonderful to work with @idmjky, @jgooten, @omarabudayyeh, and the entire team on this!
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Matteo Di Bernardo retweeted
MIT Biology is hiring faculty positions! The department seeks candidates who are developing and using computational methods to address questions in molecular, cellular, or organismal biology. academicjobsonline.org/ajo/j…
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Matteo Di Bernardo retweeted
I’m excited to share that I’ll be joining @Columbia in the CS Department as an Assistant Professor in January 2027, in New York City. My lab will work on advancing causality, AI, experimental design, and biomedical applications. I’ll be taking on PhD students and recruiting postdocs. If you’re interested in working with me, consider applying to the CS PhD program this fall or reach out at [email protected].
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Last December, Bryce Kirby and I tried to compress a genome-wide optical pooled screen into about a week, from imaging start to analysis end. Short report on that is out now in @GenomeBiology. Much still to be improved, but rapid, low-cost OPS & analysis is a possibility!
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📣 new preprint multimodal atlas. Imaging + scRNA, 57M cells. 🧬🔬 Cells are complex dynamical systems — but most ways we measure them destroy them. We asked: how does live imaging compare to scRNA-seq, the field’s gold std? The answer surprised us 🧵 biorxiv.org/content/10.64898…
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Matteo Di Bernardo retweeted
🚀 We are introducing PerturbPair (with @TakaKud0) — a platform that combines parallel Perturb-seq and optical pooled screening (OPS/PerturbView) in primary cells to systematically map at massive scale how genetic perturbations reshape cellular states across modalities. With wonderful collaborators @TakaKud0, @AnaMeireles, @AntRios, @jchuetter, @MinOta, @ORozenblattRosen, @LeviAGarraway, @KGeiger, @avtarsingh, @jkpritch, and Aviv Regev. Paper link: biorxiv.org/content/10.64898…
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Researchers at Columbia University have identified a gene that drives the development of neuroendocrine prostate cancer, an aggressive form of the disease. 👉 hubs.ly/Q04hZ8Yr0 See the original study by the Abate-Shen lab @ColumbiaMed 👉 hubs.ly/Q04hZck-0
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We've had so much fun seeing how targeted & steered interventions with Claude improve and accelerate the ways we interpret results in the @iaincheeseman lab! Very thankful to @AnthropicAI's AI for Science program for the support and for highlighting our work!
Since launching our AI for Science program, we’ve been working with scientists to understand how AI is accelerating progress. We spoke with 3 labs where Claude is reshaping research—and starting to point towards novel scientific insights and discoveries. anthropic.com/news/accelerat…
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Matteo Di Bernardo retweeted
Today @AnthropicAI released PubMed integration for Claude. No hallucinations. Just real science, real data. As a beta tester, this has been a game changer—like having a supercharged research assistant. Here are 6 prompts that will transform how you search the literature. A 🧵
We’re building tools to support research in the life sciences, from early discovery through to commercialization. With Claude for Life Sciences, we’ve added connectors to scientific tools, Skills, and new partnerships to make Claude more useful for scientific work.
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We’re @BlaineyLab sharing a major update to CROPseq-multi, our versatile system for CRISPR screens that is compatible with individual and combinatorial perturbations, diverse SpCas9-based technologies, and multiple high-content, single-cell readouts. biorxiv.org/content/10.1101/…
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🚫 No dyes. No bleaching. 🔬 Just AI + label-free microscopy = vivid virtually stained images New in @NatMachIntell: A deep learning model that enables robust virtual staining across microscopes, cell types & conditions. #CZBiohubSF @mattersOfLight explains:
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Optical pooled screening is revolutionizing functional genomics by linking genetic perturbations to complex cellular phenotypes at unprecedented scale. But analyzing these massive datasets has been a major bottleneck - researchers face fragmented tools, multiple format conversions, and lack of standardized frameworks. Together with Roshan Kern, Alexa Mallar, and Andy Nutter-Upham, we developed Brieflow, the first end-to-end computational pipeline for optical pooled screening analysis
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We validated Brieflow by reanalyzing the massive "Vesuvius" dataset: 5,072 genes across 70+ million cells with multiple phenotypic markers. Our improved pipeline uncovered functional relationships completely missed in the original study, including coherent mitochondrial gene clusters, novel ribosome biogenesis components that we experimentally validated, refined MYC transcriptional networks, and unexpected connections between mRNA processing and vesicular trafficking. We also developed MozzareLLM (github.com/cheeseman-lab/moz…) for automated biological interpretation and candidate prioritization
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Great to have you @BoWang87!
Excited to be giving a keynote at the workshop ‘AI: Advancing Foundational Biology’ hosted by @WhiteheadInst at @MIT today! I’ll be speaking about building foundation models for biomedical data, including scGPT and MedSAM. Don’t miss it!
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"AI: Advancing Foundational Biology," a symposium exploring AI's impact on biology research, is happening one week from tomorrow. Register: wi.mit.edu/events/ai-advanci…
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Check out @WhiteheadInst's symposium – AI: Advancing Foundational Biology – today (Tuesday, April 8), from 2-5:00 p.m., followed by a poster session and reception at 5 p.m. @Schmidt_Center Director Caroline Uhler will be keynoting at 2:15 p.m. Learn more: calendar.mit.edu/event/ai-ad…
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Matteo Di Bernardo retweeted
New preprint drop! Check out work from Jimmy Ly et al for how protein isoforms generated by alternate translation initiation create dual localization, contribute to mitochondrial function, and are mutated in disease. Tweet-tutorial thread below. biorxiv.org/content/10.1101/…
New preprint countdown! Mitochondria are cells within our cells. They need the same core activities - replication, transcription, translation. How do cells enable these diverse activities in both compartments? We uncover an unexpected strategy with ancient origins. Stay tuned!
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