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Wenkang Yu

dblp:191/7822 · DBLP profile ↗
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2ranked-venue papers
0as first author
0since 2021 · last 2017
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Systems, architecture and hardware · 1Applied, interdisciplinary, general and emerging computing · 1

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Computer architecture, parallel and distributed computing, and storage systems
1 paper
Memory systems · 50% GPUs and heterogeneous computing · 25% Processor architecture and microarchitecture · 25%
Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 7 heaviest of 8, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › drug discovery › drug metabolism prediction
site of metabolism prediction
0.312017
Site of metabolism prediction for oxidation reactions mediated by oxidoreductases based on chemical bond · Bioinform. 2017
Memory systems
cache
0.212016
Cache-emulated register file: An integrated on-chip memory architecture for high performance GPGPUs · MICRO 2016
GPUs and heterogeneous computing
GPU computing
0.212016
Cache-emulated register file: An integrated on-chip memory architecture for high performance GPGPUs · MICRO 2016
Memory systems › on-chip memory
on-chip memory organization
0.212016
Cache-emulated register file: An integrated on-chip memory architecture for high performance GPGPUs · MICRO 2016
Processor architecture and microarchitecture
register file
0.212016
Cache-emulated register file: An integrated on-chip memory architecture for high performance GPGPUs · MICRO 2016
Bioinformatics and computational biology › molecular informatics
cheminformatics
0.112017
Site of metabolism prediction for oxidation reactions mediated by oxidoreductases based on chemical bond · Bioinform. 2017
Bioinformatics and computational biology › systems biology › metabolic network reconstruction
metabolic reaction prediction
0.112017
Site of metabolism prediction for oxidation reactions mediated by oxidoreductases based on chemical bond · Bioinform. 2017

Methods — techniques the papers use, named apart from their topics

random forest · 0.3hybrid feature selection · 0.3ensemble classification · 0.3bayesian network · 0.3bagging · 0.3adaboost · 0.3SVM · 0.3KStar · 0.3microarchitecture modification · 0.2compiler support · 0.2ISA support · 0.2
YearPublicationVenuePosition
2017 Site of metabolism prediction for oxidation reactions mediated by oxidoreductases based on chemical bond
abstract
Motivation: The metabolites of exogenous and endogenous compounds play a pivotal role in the domain of metabolism research. However, they are still unclear for most chemicals in our environment. The in silico methods for predicting the site of metabolism (SOM) are considered to be efficient and low-cost in SOM discovery. However, many in silico methods are focused on metabolism processes catalyzed by several specified Cytochromes P450s, and only apply to substrates with special skeleton. A SOM prediction model always deserves more attention, which demands no special requirements to structures of substrates and applies to more metabolic enzymes. Results: By incorporating the use of hybrid feature selection techniques (CHI, IG, GR, Relief) and multiple classification procedures (KStar, BN, IBK, J48, RF, SVM, AdaBoostM1, Bagging), SOM prediction models for six oxidation reactions mediated by oxidoreductases were established by the integration of enzyme data and chemical bond information. The advantage of the method is the introduction of unlabeled SOM. We defined the SOM which not reported in the literature as unlabeled SOM, where negative SOM was filtered. Consequently, for each type of reaction, a series of SOM prediction models were built based on information about metabolism of 1237 heterogeneous chemicals. Then optimal models were attained through comparisons among these models. Finally, independent test set was used to validate optimal models. It demonstrated that all models gave accuracies above 0.90. For receiver operating characteristic analysis, the area under curve values of all these models over 0.906. The results suggested that these models showed good predicting power. Availability and implementation: All the models will be available when contact with [email protected]. Contacts: [email protected] or [email protected]. Supplementary information: Supplementary data are available at Bioinformatics online.
Shuaibing He, Xiaotong Ye, Wenkang Yu, Yanjiang Qiao
Bioinform.5
2016 Cache-emulated register file: An integrated on-chip memory architecture for high performance GPGPUs
abstract
The on-chip memory design is critical to the GPGPU performance because it serves between the massive threads and the huge external memory as a low-latency and high-throughput data communication point. However, the existing on-chip memory hierarchy is inherited from the conventional CPU architecture and is oftentimes sub-optimal to the SIMT (single instruction, multiple threads) execution. In this study, we surpass the traditional memory hierarchy design and reform the on-chip memory into an integrated architecture with the cache-emulated register file (RF) capability tailored for high performance GPGPU computing. With the lightweight support from ISA, compiler and the modified microarchitecture, this integrated architecture can dynamically emulate a variable-sized RF and a cache in a uniform way. Evaluation results demonstrate that this novel architecture can deliver better performance and energy efficiency with smaller on-chip memory size. For example, it can gain an average of 50% performance improvement for the cache-sensitive applications.
Naifeng Jing, Fengfeng Fan, Wenkang Yu, Li Jiang 0002, Chao Li 0009, Xiaoyao Liang
MICRO4