ITA: An Energy-Efficient Attention and Softmax Accelerator for Quantized Transformers

Transformer networks have emerged as the state-of-the-art approach for natural language processing tasks and are gaining popularity in other domains such as computer vision and audio processing. However, the efficient hardware acceleration of transformer models poses new challenges due to their high arithmetic intensities, large memory requirements, and complex dataflow dependencies. In this work, we propose ITA, a novel accelerator architecture for transformers and related models that targets efficient inference on embedded systems by exploiting 8-bit quantization and an innovative softmax implementation that operates exclusively on integer values. By computing on-the-fly in streaming mode, our softmax implementation minimizes data movement and energy consumption. ITA achieves competitive energy efficiency with respect to state-of-the-art transformer accelerators with 16.9 TOPS/W, while outperforming them in area efficiency with 5.93 TOPS/mm$^2$ in 22 nm fully-depleted silicon-on-insulator technology at 0.8 V.

Automatic detection of lesion load change in Multiple Sclerosis using convolutional neural networks with segmentation confidence

The detection of new or enlarged white-matter lesions in multiple sclerosis is a vital task in the monitoring of patients undergoing disease-modifying treatment for multiple sclerosis. However, the definition of 'new or enlarged' is not fixed, and it is known that lesion-counting is highly subjective, with high degree of inter- and intra-rater variability. Automated methods for lesion quantification hold the potential to make the detection of new and enlarged lesions consistent and repeatable. However, the majority of lesion segmentation algorithms are not evaluated for their ability to separate progressive from stable patients, despite this being a pressing clinical use-case. In this paper we show that change in volumetric measurements of lesion load alone is not a good method for performing this separation, even for highly performing segmentation methods. Instead, we propose a method for identifying lesion changes of high certainty, and establish on a dataset of longitudinal multiple sclerosis cases that this method is able to separate progressive from stable timepoints with a very high level of discrimination (AUC = 0.99), while changes in lesion volume are much less able to perform this separation (AUC = 0.71). Validation of the method on a second external dataset confirms that the method is able to generalize beyond the setting in which it was trained, achieving an accuracy of 83% in separating stable and progressive timepoints. Both lesion volume and count have previously been shown to be strong predictors of disease course across a population. However, we demonstrate that for individual patients, changes in these measures are not an adequate means of establishing no evidence of disease activity. Meanwhile, directly detecting tissue which changes, with high confidence, from non-lesion to lesion is a feasible methodology for identifying radiologically active patients.