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Devarakonda, M.

Publications and source records attributed to Devarakonda, M..

2 recordsLinked to original sources

Single Cell Foundation Models Evaluation (scFME) for In-Silico Perturbation

Foundation models pre-trained on large single-cell RNA atlases offer a compelling alternative to in-vitro experimentation for understanding gene regulatory networks and conducting gene perturbation analyses, with significant implications for target identification. Numerous foundation models have been developed, building upon early efforts such as Geneformer and scGPT. Hyperparameter optimization also results in multiple variants which require comparative analysis. Current benchmarking approaches focus on feature-based assessments or intuitive biological and statistical tasks, which may not align with the models training objectives. A recent study proposed a systematic benchmarking framework; however, its scope was limited to pre-trained (zero-shot) models. To address these limitations, we propose Single-Cell Foundation Model Evaluation (scFME)--a systematic method designed to benchmark fine-tuned foundation models for insilico perturbation (ISP). scFME ensures comprehensive and robust assessment by requiring sufficient separation between control and perturbed cells at the outset and by quantifying ISP accuracy against zero and random perturbation baselines. Furthermore, scFME enables exploration of model performance across distinct gene categories, facilitating biological interpretation and functional relevance. Using this framework, we evaluated several commonly used models (and some of their variants) and demonstrated that the methodology effectively characterizes their performance in ISP studies. Our results position scFME as a versatile and rigorous methodology for evaluating and comparing current and future foundation models.

bioinformatics↗

Evaluating Foundation Models for In-Silico Perturbation

In-silico perturbation (ISP) offers a scalable alternative to traditional gene perturbation experiments, yet evaluation of foundation models for ISP remains underexplored. We introduce a novel evaluation framework, the single cell in-silico perturbation framework (scISP), to benchmark ISP models against in-vitro experimental data using biologically meaningful metrics, including cell state separation accuracy, ISP accuracy, and mean reciprocal rank (MRR) for predicting perturbed genes. Complementary functional analyses evaluate model performance across diverse gene categories. Using scISP, we assess two well-known pre-trained foundation models, Geneformer and scGPT, alongside the deep learning model, GEARS, highlighting their respective strengths and limitations in simulating cell state transitions and identifying perturbed genes. These analyses reveal intrinsic differences across models, offering opportunities to optimize foundation models for specific biological contexts or gene categories. Our extensible framework establishes a robust bridge between computational predictions and experimental validation, advancing gene perturbation research and biological discovery.

bioinformatics↗