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Li Tan

Researcher at Brookhaven National Laboratory

Publications -  34
Citations -  278

Li Tan is an academic researcher from Brookhaven National Laboratory. The author has contributed to research in topics: Efficient energy use & Frequency scaling. The author has an hindex of 9, co-authored 34 publications receiving 216 citations. Previous affiliations of Li Tan include Los Alamos National Laboratory & University of California, Riverside.

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Journal ArticleDOI

A survey of power and energy efficient techniques for high performance numerical linear algebra operations

TL;DR: This paper surveys the research on saving power and energy for numerical linear algebra algorithms in high performance scientific computing on supercomputers around the world and summarizes state-of-the-art techniques for achieving power andEnergy efficiency in each category individually.
Proceedings ArticleDOI

Investigating the Interplay between Energy Efficiency and Resilience in High Performance Computing

TL;DR: This work presents an energy saving undervaluing approach that leverages the mainstream resilience techniques to tolerate the increased failures caused byUndervaluing, and demonstrates that this approach can save up to 12.1% energy compared to the baseline, and conserve up to 9.1%" more energy than a state-of-the-art DVFS solution.
Proceedings ArticleDOI

Design, Use and Evaluation of P-FSEFI: A Parallel Soft Error Fault Injection Framework for Emulating Soft Errors in Parallel Applications

TL;DR: A sufficiently sophisticated software fault injection framework, an application can be studied to see how it would handle many of the errors that manifest at the application level, and a developer can progressively improve the resilience at targeted locations they believe are important for their target hardware.
Posted ContentDOI

High Throughput Virtual Screening and Validation of a SARS-CoV-2 Main Protease Non-Covalent Inhibitor

TL;DR: In this paper, a novel non-covalent small-molecule inhibitor, MCULE-5948770040, that binds to and inhibits the SARS-Cov-2 main protease (Mpro) by employing a scalable high throughput virtual screening (HTVS) framework and a targeted compound library of over 6.5 million molecules that could be readily ordered and purchased.