CellMemory: Hierarchical Interpretation of Out-of-Distribution Cells Using Bottlenecked Transformer
Wang, Q.; Zhu, H.; Hu, Y.; Chen, Y.; Wang, Y.; Zhang, X.; Zou, J.; Kellis, M.; Li, Y.; Liu, D.; Jiang, L.
Show abstract
Identifying the genetic and molecular drivers of phenotypic heterogeneity among individuals is vital for understanding human health and for diagnosing, monitoring, and treating diseases. To this end, international consortia such as the Human Cell Atlas and the Tabula Sapiens are creating comprehensive cellular references. Due to the massive volume of data generated, machine learning methods, especially transformer architectures, have been widely employed in related studies. However, applying machine learning to cellular data presents several challenges. One such challenge is making the methods interpretable with respect to both the input cellular information and its context. Another less explored challenge is the accurate representation of cells outside existing references, referred to as out-of-distribution (OOD) cells. The out-of-distribution could be attributed to various physiological conditions, such as comparing diseased cells, particularly tumor cells, with healthy reference data, or significant technical variations, such as using transfer learning from single-cell reference to spatial query data. Inspired by the global workspace theory in cognitive neuroscience, we introduce CellMemory, a bottlenecked Transformer with improved generalization capabilities designed for the hierarchical interpretation of OOD cells unseen during reference building. Even without pre-training, it exceeds the performance of large language models pre-trained with tens of millions of cells. In particular, when deciphering spatially resolved single-cell transcriptomics data, CellMemory demonstrates the ability to interpret data at the granule level accurately. Finally, we harness CellMemorys robust representational capabilities to elucidate malignant cells and their founder cells in different patients, providing reliable characterizations of the cellular changes caused by the disease.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- OmicVerse: A single pipeline for exploring the entire transcriptome universe 98%
- Pathway Centric Analysis for single-cell RNA-seq and Spatial Transcriptomics Data with GSDensity 98%
- INSTINCT: Multi-sample integration of spatial chromatin accessibility sequencing data via stochastic domain translation 98%
Similar papers in this journal
- High-precision cell-type mapping and annotation of single-cell spatial transcriptomics with STAMapper 98%
- stGCL: A versatile cross-modality fusion method based on multi-modal graph contrastive learning for spatial transcriptomics 97%
- Characterizing Spatially Continuous Variations in Tissue Microenvironment through Niche Trajectory Analysis 97%
Similar papers in this journal
- SPOTlight:Seeded NMF regression to Deconvolute Spatial Transcriptomics Spots with Single-Cell Transcriptomes 98%
- Coralysis enables sensitive identification of imbalanced cell types and states in single-cell data via multi-level integration 98%
- Probabilistic cell/domain-type assignment of spatial transcriptomics data with SpatialAnno 98%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.