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Title: Simple and Automatic Distributed Machine Learning on Ray
In recent years, the pace of innovations in the fields of machine learning (ML) has accelerated, researchers in SysML have created algorithms and systems that parallelize ML training over multiple devices or computational nodes. As ML models become more structurally complex, many systems have struggled to provide all-round performance on a variety of models. Particularly, ML scale-up is usually underestimated in terms of the amount of knowledge and time required to map from an appropriate distribution strategy to the model. Applying parallel training systems to complex models adds nontrivial development overheads in addition to model prototyping, and often results in lower-than-expected performance. This tutorial identifies research and practical pain points in parallel ML training, and discusses latest development of algorithms and systems on addressing these challenges in both usability and performance. In particular, this tutorial presents a new perspective of unifying seemingly different distributed ML training strategies. Based on it, introduces new techniques and system architectures to simplify and automate ML parallelization. This tutorial is built upon the authors' years' of research and industry experience, comprehensive literature survey, and several latest tutorials and papers published by the authors and peer researchers. The tutorial consists of four parts. The first part will present a landscape of distributed ML training techniques and systems, and highlight the major difficulties faced by real users when writing distributed ML code with big model or big data. The second part dives deep to explain the mainstream training strategies, guided with real use case. By developing a new and unified formulation to represent the seemingly different data- and model- parallel strategies, we describe a set of techniques and algorithms to achieve ML auto-parallelization, and compiler system architectures for auto-generating and exercising parallelization strategies based on models and clusters. The third part of this tutorial exposes a hidden layer of practical pain points in distributed ML training: hyper-parameter tuning and resource allocation, and introduces techniques to improve these aspects. The fourth part is designed as a hands-on coding session, in which we will walk through the audiences on writing distributed training programs in Python, using the various distributed ML tools and interfaces provided by the Ray ecosystem.  more » « less
Award ID(s):
1730628
NSF-PAR ID:
10310459
Author(s) / Creator(s):
; ; ;
Date Published:
Journal Name:
KDD '21: Proceedings of the 27th ACM SIGKDD Conference on Knowledge Discovery & Data Mining
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
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The breast corpus subset should be released by November 2021. By December 2021 we should also release the unannotated FCCC data. We are currently annotating urinary tract data as well. We expect to release about 5,600 processed TUH slides in this subset. We have an additional 53,000 unprocessed TUH slides digitized. Corpora of this size will stimulate the development of a new generation of deep learning technology. In clinical settings where resources are limited, an assistive diagnoses model could support pathologists’ workload and even help prioritize suspected cancerous cases. ACKNOWLEDGMENTS This material is supported by the National Science Foundation under grants nos. CNS-1726188 and 1925494. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect the views of the National Science Foundation. REFERENCES [1] N. Shawki et al., “The Temple University Digital Pathology Corpus,” in Signal Processing in Medicine and Biology: Emerging Trends in Research and Applications, 1st ed., I. Obeid, I. Selesnick, and J. Picone, Eds. New York City, New York, USA: Springer, 2020, pp. 67 104. https://www.springer.com/gp/book/9783030368432. [2] J. Picone, T. Farkas, I. Obeid, and Y. Persidsky, “MRI: High Performance Digital Pathology Using Big Data and Machine Learning.” Major Research Instrumentation (MRI), Division of Computer and Network Systems, Award No. 1726188, January 1, 2018 – December 31, 2021. https://www. isip.piconepress.com/projects/nsf_dpath/. [3] A. Gulati et al., “Conformer: Convolution-augmented Transformer for Speech Recognition,” in Proceedings of the Annual Conference of the International Speech Communication Association (INTERSPEECH), 2020, pp. 5036-5040. https://doi.org/10.21437/interspeech.2020-3015. [4] C.-J. Wu et al., “Machine Learning at Facebook: Understanding Inference at the Edge,” in Proceedings of the IEEE International Symposium on High Performance Computer Architecture (HPCA), 2019, pp. 331–344. https://ieeexplore.ieee.org/document/8675201. [5] I. Caswell and B. Liang, “Recent Advances in Google Translate,” Google AI Blog: The latest from Google Research, 2020. [Online]. Available: https://ai.googleblog.com/2020/06/recent-advances-in-google-translate.html. [Accessed: 01-Aug-2021]. [6] V. Khalkhali, N. Shawki, V. Shah, M. Golmohammadi, I. Obeid, and J. Picone, “Low Latency Real-Time Seizure Detection Using Transfer Deep Learning,” in Proceedings of the IEEE Signal Processing in Medicine and Biology Symposium (SPMB), 2021, pp. 1 7. https://www.isip. piconepress.com/publications/conference_proceedings/2021/ieee_spmb/eeg_transfer_learning/. [7] J. Picone, T. Farkas, I. Obeid, and Y. Persidsky, “MRI: High Performance Digital Pathology Using Big Data and Machine Learning,” Philadelphia, Pennsylvania, USA, 2020. https://www.isip.piconepress.com/publications/reports/2020/nsf/mri_dpath/. [8] I. Hunt, S. Husain, J. Simons, I. Obeid, and J. Picone, “Recent Advances in the Temple University Digital Pathology Corpus,” in Proceedings of the IEEE Signal Processing in Medicine and Biology Symposium (SPMB), 2019, pp. 1–4. https://ieeexplore.ieee.org/document/9037859. [9] A. P. Martinez, C. Cohen, K. Z. Hanley, and X. (Bill) Li, “Estrogen Receptor and Cytokeratin 5 Are Reliable Markers to Separate Usual Ductal Hyperplasia From Atypical Ductal Hyperplasia and Low-Grade Ductal Carcinoma In Situ,” Arch. Pathol. Lab. Med., vol. 140, no. 7, pp. 686–689, Apr. 2016. https://doi.org/10.5858/arpa.2015-0238-OA. 
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