Paper List
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Discovery of a Hematopoietic Manifold in scGPT Yields a Method for Extracting Performant Algorithms from Biological Foundation Model Internals
This work addresses the core challenge of extracting reusable, interpretable, and high-performance biological algorithms from the opaque internal repr...
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MS2MetGAN: Latent-space adversarial training for metabolite–spectrum matching in MS/MS database search
This paper addresses the critical bottleneck in metabolite identification: the generation of high-quality negative training samples that are structura...
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Toward Robust, Reproducible, and Widely Accessible Intracranial Language Brain-Computer Interfaces: A Comprehensive Review of Neural Mechanisms, Hardware, Algorithms, Evaluation, Clinical Pathways and Future Directions
This review addresses the core challenge of fragmented and heterogeneous evidence that hinders the clinical translation of intracranial language BCIs,...
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Less Is More in Chemotherapy of Breast Cancer
通过纳入细胞周期时滞和竞争项,解决了现有肿瘤-免疫模型的过度简化问题,以定量比较化疗方案。
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Fold-CP: A Context Parallelism Framework for Biomolecular Modeling
This paper addresses the critical bottleneck of GPU memory limitations that restrict AlphaFold 3-like models to processing only a few thousand residue...
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Open Biomedical Knowledge Graphs at Scale: Construction, Federation, and AI Agent Access with Samyama Graph Database
This paper addresses the core pain point of fragmented biomedical data by constructing and federating large-scale, open knowledge graphs to enable sea...
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Predictive Analytics for Foot Ulcers Using Time-Series Temperature and Pressure Data
This paper addresses the critical need for continuous, real-time monitoring of diabetic foot health by developing an unsupervised anomaly detection fr...
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Hypothesis-Based Particle Detection for Accurate Nanoparticle Counting and Digital Diagnostics
This paper addresses the core challenge of achieving accurate, interpretable, and training-free nanoparticle counting in digital diagnostic assays, wh...
A Standardized Framework for Evaluating Gene Expression Generative Models
University of Cambridge | Wellcome Sanger Institute | Sapienza University of Rome | ISTI-CNR
30秒速读
IN SHORT: This paper addresses the critical lack of standardized evaluation protocols for single-cell gene expression generative models, where inconsistent metric implementations and computation spaces make cross-study comparisons impossible.
核心创新
- Methodology Introduces GGE, the first unified Python framework with explicit computation space parameterization (raw, PCA, DEG-restricted) for standardized evaluation of generative models.
- Methodology Proposes perturbation-effect correlation metric that measures direction and magnitude of perturbation responses rather than raw expression correlation, focusing evaluation on biologically relevant signals.
- Methodology Demonstrates that Wasserstein distance values vary by nearly an order of magnitude (17.2 to 104.3) depending solely on computation space, quantifying the standardization problem.
主要结论
- Metric values vary substantially with implementation choices: W₂ distance ranges from 17.2 (PCA-25) to 104.3 (raw space) on identical data, highlighting critical need for standardization.
- DEG selection strategy affects correlation metrics: top-20 DEG selection yields Pearson correlation of 0.614±0.066 vs strict threshold selection (lfc>1, p<0.01) yielding 0.506±0.217 on Norman dataset.
- Perturbation-effect correlation in DEG space provides biologically meaningful evaluation, focusing on genes that actually respond to perturbations rather than steady-state background expression.
摘要: The rapid development of generative models for single-cell gene expression data has created an urgent need for standardised evaluation frameworks. Current evaluation practices suffer from inconsistent metric implementations, incomparable hyperparameter choices, and a lack of biologically-grounded metrics. We present Generated Genetic Expression Evaluator (GGE), an open-source Python framework that addresses these challenges by providing a comprehensive suite of distributional metrics with explicit computation space options and biologically-motivated evaluation through differentially expressed gene (DEG)-focused analysis and perturbation-effect correlation, enabling standardized reporting and reproducible benchmarking. Through extensive analysis of the single-cell generative modeling literature, we identify that no standardized evaluation protocol exists. Methods report incomparable metrics computed in different spaces with different hyperparameters. We demonstrate that metric values vary substantially depending on implementation choices, highlighting the critical need for standardization. GGE enables fair comparison across generative approaches and accelerates progress in perturbation response prediction, cellular identity modeling, and counterfactual inference.