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Nasrin Akbari

Publications and source records attributed to Nasrin Akbari.

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Towards Brain MRI Foundation Models for the Clinic: Findings from the FOMO25 Challenge

Clinical deployment of automated brain MRI analysis faces a fundamental challenge: clinical data is heterogeneous and noisy, and high-quality labels are prohibitively costly to obtain. Self-supervised learning (SSL) can address this by leveraging the vast amounts of unlabeled data produced in clinical workflows to train robust \textit{foundation models} that adapt out-of-domain with minimal supervision. However, the development of foundation models for brain MRI has been limited by small pretraining datasets and in-domain benchmarking focused on high-quality, research-grade data. To address this gap, we organized the FOMO25 challenge as a satellite event at MICCAI 2025. FOMO25 provided participants with a large pretraining dataset, FOMO60K, and evaluated models on data sourced directly from clinical workflows in few-shot and out-of-domain settings. Tasks covered infarct classification, meningioma segmentation, and brain age regression, and considered both models trained on FOMO60K (method track) and any data (open track). Nineteen foundation models from sixteen teams were evaluated using a standardized containerized pipeline. Results show that (a) self-supervised pretraining improves generalization on clinical data under domain shift, with the strongest models trained \textit{out-of-domain} surpassing supervised baselines trained \textit{in-domain}. (b) No single pretraining objective benefits all tasks: MAE favors segmentation, hybrid reconstruction-contrastive objectives favor classification, and (c) strong performance was achieved by small pretrained models, and improvements from scaling model size and training duration did not yield reliable benefits.

cs.CV

A Customized Memory-aware Architecture for Biological Sequence Alignment

Sequence alignment is a fundamental process in computational biology which identifies regions of similarity in biological sequences. With the exponential growth in the volume of data in bioinformatics databases, the time, processing power, and memory bandwidth for comparing a query sequence with the available databases grows proportionally. The sequence alignment algorithms often involve simple arithmetic operations and feature high degrees of inherent fine-grained and coarse-grained parallelism. These features can be potentially exploited by a massive parallel processor, such as a GPU, to increase throughput. In this paper, we show that the excessive memory bandwidth demand of the sequence alignment algorithms prevents exploiting the maximum achievable throughput on conventional parallel machines. We then propose a memory-aware architecture to reduce the bandwidth demand of the sequence alignment algorithms, effectively pushing the memory wall to extract higher throughput. The design is integrated at the logic layer of an emerging 3D DRAM as a processing-in-memory architecture to further increase the available bandwidth. The experimental results show that the proposed architecture results in up to 2.4x speedup over a GPU-based design. Moreover, by moving the computation closer to the memory, power consumption is reduced by 37%, on average.

cs.AR