Zhenya Zang, Quan Wang, Mingliang Pan, Yuanzhe Zhang, Xi Chen, Xingda Li, David Day Uei Li
{"title":"实现高性能深度学习架构和硬件加速器设计,用于漫射相关光谱学的稳健分析。","authors":"Zhenya Zang, Quan Wang, Mingliang Pan, Yuanzhe Zhang, Xi Chen, Xingda Li, David Day Uei Li","doi":"10.1016/j.cmpb.2024.108471","DOIUrl":null,"url":null,"abstract":"<div><div>This study proposes a compact deep learning (DL) architecture and a highly parallelized computing hardware platform to reconstruct the blood flow index (BFi) in diffuse correlation spectroscopy (DCS). We leveraged a rigorous analytical model to generate autocorrelation functions (ACFs) to train the DL network. We assessed the accuracy of the proposed DL using simulated and milk phantom data. Compared to convolutional neural networks (CNN), our lightweight DL architecture achieves 66.7% and 18.5% improvement in MSE for BFi and the coherence factor <em>β</em>, using synthetic data evaluation. The accuracy of rBFi over different algorithms was also investigated. We further simplified the DL computing primitives using subtraction for feature extraction, considering further hardware implementation. We extensively explored computing parallelism and fixed-point quantization within the DL architecture. With the DL model's compact size, we employed unrolling and pipelining optimizations for computation-intensive for-loops in the DL model while storing all learned parameters in on-chip BRAMs. We also achieved pixel-wise parallelism, enabling simultaneous, real-time processing of 10 and 15 autocorrelation functions on Zynq-7000 and Zynq-UltraScale+ field programmable gate array (FPGA), respectively. Unlike existing FPGA accelerators that produce BFi and the <em>β</em> from autocorrelation functions on standalone hardware, our approach is an encapsulated, end-to-end on-chip conversion process from intensity photon data to the temporal intensity ACF and subsequently reconstructing BFi and <em>β</em>. This hardware platform achieves an on-chip solution to replace post-processing and miniaturize modern DCS systems that use single-photon cameras. We also comprehensively compared the computational efficiency of our FPGA accelerator to CPU and GPU solutions.</div></div>","PeriodicalId":10624,"journal":{"name":"Computer methods and programs in biomedicine","volume":"258 ","pages":"Article 108471"},"PeriodicalIF":4.9000,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Towards high-performance deep learning architecture and hardware accelerator design for robust analysis in diffuse correlation spectroscopy\",\"authors\":\"Zhenya Zang, Quan Wang, Mingliang Pan, Yuanzhe Zhang, Xi Chen, Xingda Li, David Day Uei Li\",\"doi\":\"10.1016/j.cmpb.2024.108471\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>This study proposes a compact deep learning (DL) architecture and a highly parallelized computing hardware platform to reconstruct the blood flow index (BFi) in diffuse correlation spectroscopy (DCS). We leveraged a rigorous analytical model to generate autocorrelation functions (ACFs) to train the DL network. We assessed the accuracy of the proposed DL using simulated and milk phantom data. Compared to convolutional neural networks (CNN), our lightweight DL architecture achieves 66.7% and 18.5% improvement in MSE for BFi and the coherence factor <em>β</em>, using synthetic data evaluation. The accuracy of rBFi over different algorithms was also investigated. We further simplified the DL computing primitives using subtraction for feature extraction, considering further hardware implementation. We extensively explored computing parallelism and fixed-point quantization within the DL architecture. With the DL model's compact size, we employed unrolling and pipelining optimizations for computation-intensive for-loops in the DL model while storing all learned parameters in on-chip BRAMs. We also achieved pixel-wise parallelism, enabling simultaneous, real-time processing of 10 and 15 autocorrelation functions on Zynq-7000 and Zynq-UltraScale+ field programmable gate array (FPGA), respectively. Unlike existing FPGA accelerators that produce BFi and the <em>β</em> from autocorrelation functions on standalone hardware, our approach is an encapsulated, end-to-end on-chip conversion process from intensity photon data to the temporal intensity ACF and subsequently reconstructing BFi and <em>β</em>. This hardware platform achieves an on-chip solution to replace post-processing and miniaturize modern DCS systems that use single-photon cameras. We also comprehensively compared the computational efficiency of our FPGA accelerator to CPU and GPU solutions.</div></div>\",\"PeriodicalId\":10624,\"journal\":{\"name\":\"Computer methods and programs in biomedicine\",\"volume\":\"258 \",\"pages\":\"Article 108471\"},\"PeriodicalIF\":4.9000,\"publicationDate\":\"2024-10-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Computer methods and programs in biomedicine\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0169260724004644\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Computer methods and programs in biomedicine","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0169260724004644","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS","Score":null,"Total":0}
Towards high-performance deep learning architecture and hardware accelerator design for robust analysis in diffuse correlation spectroscopy
This study proposes a compact deep learning (DL) architecture and a highly parallelized computing hardware platform to reconstruct the blood flow index (BFi) in diffuse correlation spectroscopy (DCS). We leveraged a rigorous analytical model to generate autocorrelation functions (ACFs) to train the DL network. We assessed the accuracy of the proposed DL using simulated and milk phantom data. Compared to convolutional neural networks (CNN), our lightweight DL architecture achieves 66.7% and 18.5% improvement in MSE for BFi and the coherence factor β, using synthetic data evaluation. The accuracy of rBFi over different algorithms was also investigated. We further simplified the DL computing primitives using subtraction for feature extraction, considering further hardware implementation. We extensively explored computing parallelism and fixed-point quantization within the DL architecture. With the DL model's compact size, we employed unrolling and pipelining optimizations for computation-intensive for-loops in the DL model while storing all learned parameters in on-chip BRAMs. We also achieved pixel-wise parallelism, enabling simultaneous, real-time processing of 10 and 15 autocorrelation functions on Zynq-7000 and Zynq-UltraScale+ field programmable gate array (FPGA), respectively. Unlike existing FPGA accelerators that produce BFi and the β from autocorrelation functions on standalone hardware, our approach is an encapsulated, end-to-end on-chip conversion process from intensity photon data to the temporal intensity ACF and subsequently reconstructing BFi and β. This hardware platform achieves an on-chip solution to replace post-processing and miniaturize modern DCS systems that use single-photon cameras. We also comprehensively compared the computational efficiency of our FPGA accelerator to CPU and GPU solutions.
期刊介绍:
To encourage the development of formal computing methods, and their application in biomedical research and medical practice, by illustration of fundamental principles in biomedical informatics research; to stimulate basic research into application software design; to report the state of research of biomedical information processing projects; to report new computer methodologies applied in biomedical areas; the eventual distribution of demonstrable software to avoid duplication of effort; to provide a forum for discussion and improvement of existing software; to optimize contact between national organizations and regional user groups by promoting an international exchange of information on formal methods, standards and software in biomedicine.
Computer Methods and Programs in Biomedicine covers computing methodology and software systems derived from computing science for implementation in all aspects of biomedical research and medical practice. It is designed to serve: biochemists; biologists; geneticists; immunologists; neuroscientists; pharmacologists; toxicologists; clinicians; epidemiologists; psychiatrists; psychologists; cardiologists; chemists; (radio)physicists; computer scientists; programmers and systems analysts; biomedical, clinical, electrical and other engineers; teachers of medical informatics and users of educational software.