aiqbench analysis
This research establishes the first two-exponent scaling law for single-cell foundation models, demonstrating how causal transformers paired with quantized VAE tokenizers can generate biologically faithful gene expression vectors. By optimizing compute frontiers and validating biological fidelity against ground truth distributions, the study provides a rigorous framework for future finetuning tasks like perturbation response prediction in genomics.
Scaling an Autoregressive Transformer for Single-Cell Generation
arXiv:2608.02961v1 Announce Type: new Abstract: We study a self-supervised generation task for single-cell gene expression vectors: given a set of vectors from a cell type, we aim to generate additional gene expression vectors of that cell type. For this task we characterize both the biological fidelity of the generated gene expression vectors and the scaling behavior of the pretraining loss. The model is a causal transformer paired with a learned quantized VAE tokenizer, trained with a cross-entropy loss. To evaluate the model, we condition it on held-out gene expression vectors of a cell type and generate vectors of gene expression, comparing the resulting distribution over gene expression vectors to the ground truth distribution of that cell type. We study the scaling properties of the proposed architecture by varying the number of trained parameters and the amount of training data. To our knowledge, we find the first jointly-fit two-exponent scaling law and compute-optimal frontier for a single-cell foundation model. Finally, we discuss how this pretrained model could be finetuned for perturbation response prediction.
Abstract:We study a self-supervised generation task for single-cell gene expression vectors: given a set of vectors from a cell type, we aim to generate additional gene expression vectors of that cell type. For this task we characterize both the biological fidelity of the generated gene expression vectors and the scaling behavior of the pretraining loss. The model is a causal transformer paired with a learned quantized VAE tokenizer, trained with a cross-entropy loss. To evaluate the model, we condition it on held-out gene expression vectors of a cell type and generate vectors of gene expression, comparing the resulting distribution over gene expression vectors to the ground truth distribution of that cell type. We study the scaling properties of the proposed architecture by varying the number of trained parameters and the amount of training data. To our knowledge, we find the first jointly-fit two-exponent scaling law and compute-optimal frontier for a single-cell foundation model. Finally, we discuss how this pretrained model could be finetuned for perturbation response prediction.
Machine Learning (cs.LG); Artificial Intelligence (cs.AI); Genomics (q-bio.GN)
arXiv:2608.02961 [cs.LG]
(or arXiv:2608.02961v1 [cs.LG] for this version)
https://doi.org/10.48550/arXiv.2608.02961 Focus to learn more arXiv-issued DOI via DataCite (pending registration)
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