个性化癌症治疗的可重构概率AI架构

S. Kulkarni, Sachin Bhat, C. A. Moritz
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引用次数: 1

摘要

生命的机制是通过基因和蛋白质之间复杂的相互作用来运作的。捕捉这些相互作用的尝试最终导致了基因网络的研究。基因缺陷会导致错误的相互作用,进而导致疾病。为了对这些疾病进行个性化治疗,需要对遗传网络和患者的遗传数据进行仔细分析。在这项工作中,我们共同设计了一个新的概率人工智能模型以及一个可重构的架构,以实现对癌症患者的个性化治疗。这种方法为广泛使用个性化医疗提供了具有成本效益和可扩展的解决方案。我们的模型在其预测中提供了可解释性和现实的信心,这对医学应用至关重要。在3000名患者的数据集上得出的个性化推断与80%的病例中医生的治疗选择一致。其他病例偏离了通用指南,使基于遗传数据的个性化治疗方案成为可能。我们的架构在混合SoC-FPGA平台上进行了验证,该平台在16核至强工作站上实现,速度比软件快25倍,功耗低25倍。
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Reconfigurable Probabilistic AI Architecture for Personalized Cancer Treatment
The machinery of life operates on the complex interactions between genes and proteins. Attempts to capture these interactions have culminated into the study of Genetic Networks. Genetic defects lead to erroneous interactions, which in turn lead to diseases. For personalized treatment of these diseases, a careful analysis of Genetic Networks and a patient's genetic data is required. In this work, we co-design a novel probabilistic AI model along with a reconfigurable architecture to enable personalized treatment for cancer patients. This approach enables a cost-effective and scalable solution for widespread use of personalized medicine. Our model offers interpretability and realistic confidences in its predictions, which is essential for medical applications. The resulting personalized inference on a dataset of 3k patients agrees with doctor's treatment choices in 80% of the cases. The other cases are diverging from the universal guideline, enabling individualized treatment options based on genetic data. Our architecture is validated on a hybrid SoC-FPGA platform which performs 25× faster than software, implemented on a 16-core Xeon workstation, while consuming 25× less power.
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