Join us on the Venture Scientist Bootcamp, a full time, 4-month incubator at Mila, built specifically for deep tech founders with elite STEM backgrounds.
Learn how to leverage generative AI to support and improve your productivity at work. The next cohort will take place online on April 28 and 30, 2026, in French.
We use cookies to analyze the browsing and usage of our website and to personalize your experience. You can disable these technologies at any time, but this may limit certain functionalities of the site. Read our Privacy Policy for more information.
Setting cookies
You can enable and disable the types of cookies you wish to accept. However certain choices you make could affect the services offered on our sites (e.g. suggestions, personalised ads, etc.).
Essential cookies
These cookies are necessary for the operation of the site and cannot be deactivated. (Still active)
Analytics cookies
Do you accept the use of cookies to measure the audience of our sites?
Multimedia Player
Do you accept the use of cookies to display and allow you to watch the video content hosted by our partners (YouTube, etc.)?
A central goal of single-cell transcriptomics is to reconstruct dynamic cellular processes from static scRNA-seq snapshots, yet most traject… (see more)ory inference methods rely on transcriptomic similarity as a proxy for developmental linkage — an assumption that frequently fails. While lineage tracing overcomes this limitation, it requires genetic perturbations and specialized longitudinal designs. In adaptive immune cells, T and B cell receptors (AIRs) naturally encode clonal ancestry and are routinely sequenced alongside the transcriptome, providing lineage information in standard snapshot datasets, but existing trajectory methods are not adapted to exploit this signal. Here, we lay the foundation for incorporating AIR-encoded lineage information into trajectory inference by biasing RNA-based diffusion maps toward AIR-consistent paths, thereby integrating lineage constraints into learned cell-state representations. Across simulations of increasing complexity, our multimodal approach recovers more biologically plausible trajectories than RNA-only baselines. While optimized for lymphocyte differentiation, the framework generalizes to other endogenous lineage barcodes, such as mitochondrial mutations.
2026-03-03
LMRL @ International Conference on Learning Representations (poster)