--- license: mit library_name: assayloop tags: - biology - genomics - crispr - active-learning - drug-discovery pipeline_tag: other --- # AssayFormer [Website](https://genentech.github.io/AssayLoop) | [Models and Data](https://huggingface.co/collections/Genentech/assaybench) | [Paper](https://arxiv.org/abs/2609.11877) | [![Benchmark Package](https://img.shields.io/pypi/v/assaybench)](https://pypi.org/project/assaybench/) ![The task: a screen is a library of genes, a phenotype and a hit set. Each round, a method sees the phenotype and everything it has already assayed, and chooses the next hundred genes.](https://raw.githubusercontent.com/Genentech/AssayLoop/main/docs/assets/figures/figure1.png) The amortized gene ranker from **AssayLoop**: *Biology-in-the-loop: Amortized Adaptive Hit Discovery in CRISPR Screens*. Given a screen description and the hit labels revealed so far, it scores every gene in a 24,217-gene vocabulary and proposes the next batch to assay. In the paper, a 21,147 gene subset was used. ## Usage ```python from huggingface_hub import snapshot_download from assayloop.models.amortized_ranker import AmortizedRankerModel ckpt = snapshot_download("Genentech/assayformer") model = AmortizedRankerModel(checkpoint=ckpt, ckpt_file="model_last.pt") ``` Note the explicit `ckpt_file`: the loader defaults to `model.pt`, which is not in this repository. Then run it on a held-out screen and score the trajectory: ```python from assaybench import SequentialLoop, enrichment_factor, gene_universe, load_screens from assayloop.acquisitions.greedy_from_model import GreedyFromModel from assayloop.tasks import AssayBenchGeneBatchTask screens = load_screens("assayloop-test") # the paper's 20-screen test set universe = gene_universe(screens) # the f2 pool, 21,147 genes screen = screens[0] task = AssayBenchGeneBatchTask(screen, universe_genes=universe) run = SequentialLoop(task, model, GreedyFromModel(), metrics=[], batch_size=100).run(n_steps=10) picked = [g for step in run.history for g in step.acquired_batch] hits = [g for g, h in zip(screen.genes, screen.hits) if h] print(enrichment_factor(picked, screen.genes, hits, universe=universe, budget=1000)) # 7.61 on U_1733_merged ``` ## Results | metric | value | |---|---| | Enrichment factor (EF, domain-adjusted) | 4.83 | | Fraction of hits recovered at budget 1000 | 0.232 | | Domain-adjusted nAUC | 0.172 | | Picks outside the screen's library | 0.100 | | DepMap common-essential fraction | 0.407 | | Effective pathways EP-B / EP-S / EP-D | 19.3 / 46.7 / 65.0 | ## Files | file | what | |---|---| | `model_last.pt` | weights — 5,033,117 parameters, the final GRPO epoch | | `config.json` | architecture and RL hyperparameters | | `vocab.json` | the 24,217-entry gene vocabulary (index 0 is ``) | `model_last.pt` is the checkpoint the paper reports. If you want the gene embedding table on its own it is `state_dict["gene_emb.weight"]`, shape (24217, 10). ## Architecture A 3-layer transformer encoder over a sequence of observed (gene, label) pairs plus the screen description, scoring candidates by dot product against a learned gene embedding. | | | |---|---| | encoder | 3 layers, `d_model` 384, 2 heads, FFN 1024, no dropout | | gene embeddings | 24,217 × 10, initialised from a K=10 BPMF fit | | description | 1536-d, projected to 384 | | context | up to 1024 observations | **The description input is a precomputed embedding, not text.** The model expects a 1536-d vector from OpenAI `text-embedding-3-small`. The repository ships the screen-description embeddings for the benchmark screens, so you only need an embedding backend for screens of your own. ## Citation ```bibtex @article{edwards2026biologyloop, title={Biology-in-the-loop: Amortized Adaptive Hit Discovery in CRISPR Screens}, author={Edwards, Carl and De Brouwer, Edward and Li, Xiner and Lee, Namkyeong and Hajiramezanali, Ehsan and Biton, Anne and Mostafavi, Sara and Scalia, Gabriele}, journal={arXiv preprint arXiv:2609.11877}, url={https://arxiv.org/abs/2609.11877}, year={2026} } ``` Licensed MIT, © 2026 Genentech, Inc.