Jeremie Kalfon 👨‍💻🧬🤖🚀

@jkobject.com

Doing a Ph.D. AI in Bio. | Ex @WhiteLabGx @BroadInstitute @MIT | Built @PiPleteam | ML, Cancer, Genomics, Data Sci, Entrepreneur, FullStack Dev | All views are mine

Science has a weird habit: we still treat the PDF as the atomic unit of trust. But a paper is not one thing. It is a bundle of datasets, tools, models, protocols, results, assumptions, proofs, bugs, caveats, and human story. AI makes this harder to ignore. 1/3

I made a map of gene regulation as one integrated control system, from DNA → RNA → protein. 🧬 It contains 38 mechanisms grouped into 7 layers. It has a few recurring principles, such as: 🔓 accessibility 🏷️ reversible marks ⏱️ and kinetic coupling. 1/2

In fall 2023, I met Alex in CZI's CellXGene Slack channel when we were both trying to figure out how to best manage metadata of thousands of scRNA-seq datasets. Alex for his work on LaminDB, and I for my work on scRNA-seq foundation models. 1/3

The biggest bottleneck in building cell foundation models isn't the architecture. It's the data. For scPRINT-2 we assembled what is, to our knowledge, the largest pre-training corpus for any cell foundation model. www.biorxiv.org/cont... 🧵 1/3

scPRINT-2: Towards the next-generation of cell foundation models and benchmarks | bioRxiv

bioRxiv - the preprint server for biology, operated by openRxiv, a nonprofit organization dedicated to advancing scientific communication

biorxiv.org

Self-attention changed everything in deep learning. But it comes with a tax: O(n²) complexity. For long sequences, that's not just slow — it's a wall. There's a cleaner way to think about it, which I introduced in my recent preprint: scPRINT-2, it is called Criss-Cross Attention: 🧵 1/2

🌐🧬I am excited to present you a round table I am doing together with Matteo Marengo Gabriel Michaux as part of our emerging Nucleate Parisian chapter led by Clara Brouaux 🔥. Title: **Inside AI: Choosing the Right Path to Value Creation** 1/3

In 2025, deciding to have a child without full genome sequencing of both parents is borderline reckless. It costs under €400. Takes 2 minutes. Could save your child’s life. Yet >200 million people live with rare genetic diseases—many preventable by this simple test. 1/2