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Ruogu Ding

dblp:09/10619 · DBLP profile ↗
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4ranked-venue papers
1as first author
1since 2021 · last 2026
—ORCID · none

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

Databases, data management, data science and information retrieval · 2Artificial intelligence and machine learning · 1 · 1 first-author · 1 since 2021Graphics, computer vision, multimedia, augmented reality and games · 1 · 1 first-author · 1 since 2021Applied, 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
Electronic design automation · 100%
Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%
Databases, data mining, and information retrieval
1 paper
Spatial and temporal data management · 100%

Topics — the 9 heaviest of 9, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Electronic design automation
design space exploration
1.012026
PrefixGPT: Prefix Adder Optimization by a Generative Pre-trained Transformer · AAAI 2026
Electronic design automation
hardware verification and test
1.012026
PrefixGPT: Prefix Adder Optimization by a Generative Pre-trained Transformer · AAAI 2026
Electronic design automation
logic synthesis
1.012026
PrefixGPT: Prefix Adder Optimization by a Generative Pre-trained Transformer · AAAI 2026
Spatial and temporal data management
trajectory data management
0.212014
Personalized trajectory matching in spatial networks · VLDB J. 2014
Spatial and temporal data management › trajectory analysis
trajectory matching
0.212014
Personalized trajectory matching in spatial networks · VLDB J. 2014
Bioinformatics and computational biology › sequence analysis › sequence assembly › genome assembly
de novo assembly
0.112012
A de novo metagenomic assembly program for shotgun DNA reads · Bioinform. 2012
Bioinformatics and computational biology
metagenomics
0.112012
A de novo metagenomic assembly program for shotgun DNA reads · Bioinform. 2012
Bioinformatics and computational biology › sequence analysis › sequence assembly › genome assembly › de novo assembly
overlap-layout-consensus
0.112012
A de novo metagenomic assembly program for shotgun DNA reads · Bioinform. 2012
Bioinformatics and computational biology › genomics › DNA sequencing
shotgun sequencing
0.012012
A de novo metagenomic assembly program for shotgun DNA reads · Bioinform. 2012

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

legality mask · 1.0generative pre-trained transformer · 1.0decoder-only transformer · 1.0overlap/layout/consensus · 0.1mate pair information · 0.1
YearPublicationVenuePosition
2026 PrefixGPT: Prefix Adder Optimization by a Generative Pre-trained Transformer
abstract
Prefix adders are widely used in compute-intensive applications for their high speed. However, designing optimized prefix adders is challenging due to strict design rules and an exponentially large design space. We introduce PrefixGPT, a generative pre-trained Transformer (GPT) that directly generates optimized prefix adders from scratch. Our approach represents an adder's topology as a two-dimensional coordinate sequence and applies a legality mask during generation, ensuring every design is valid by construction. PrefixGPT features a customized decoder-only Transformer architecture. The model is first pre-trained on a corpus of randomly synthesized valid prefix adders to learn design rules and then fine-tuned to navigate the design space for optimized design quality. Compared with existing works, PrefixGPT not only finds a new optimal design with a 7.7% improved area-delay product (ADP) but exhibits superior exploration quality, lowering the average ADP by up to 79.1%. This demonstrates the potential of GPT-style models to first master complex hardware design principles and then apply them for more efficient design optimization.
Ruogu Ding, Ulf Schlichtmann, Weikang Qian
AAAI1
2014 Personalized trajectory matching in spatial networks
Shuo Shang, Ruogu Ding, Kai Zheng 0001, Christian S. Jensen, Panos Kalnis, Xiaofang Zhou 0001
VLDB J.2
2012 User oriented trajectory search for trip recommendation
abstract
Trajectory sharing and searching have received significant attentions in recent years. In this paper, we propose and investigate a novel problem called User Oriented Trajectory Search (UOTS) for trip recommendation. In contrast to conventional trajectory search by locations (spatial domain only), we consider both spatial and textual domains in the new UOTS query. Given a trajectory data set, the query input contains a set of intended places given by the traveler and a set of textual attributes describing the traveler's preference. If a trajectory is connecting/close to the specified query locations, and the textual attributes of the trajectory are similar to the traveler'e preference, it will be recommended to the traveler for reference. This type of queries can bring significant benefits to travelers in many popular applications such as trip planning and recommendation.
Shuo Shang, Ruogu Ding, Bo Yuan 0003, Kexin Xie, Kai Zheng 0001, Panos Kalnis
EDBT2
2012 A de novo metagenomic assembly program for shotgun DNA reads
abstract
MOTIVATION: A high-quality assembly of reads generated from shotgun sequencing is a substantial step in metagenome projects. Although traditional assemblers have been employed in initial analysis of metagenomes, they cannot surmount the challenges created by the features of metagenomic data. RESULT: We present a de novo assembly approach and its implementation named MAP (metagenomic assembly program). Based on an improved overlap/layout/consensus (OLC) strategy incorporated with several special algorithms, MAP uses the mate pair information, resulting in being more applicable to shotgun DNA reads (recommended as >200 bp) currently widely used in metagenome projects. Results of extensive tests on simulated data show that MAP can be superior to both Celera and Phrap for typical longer reads by Sanger sequencing, as well as has an evident advantage over Celera, Newbler and the newest Genovo, for typical shorter reads by 454 sequencing. AVAILABILITY AND IMPLEMENTATION: The source code of MAP is distributed as open source under the GNU GPL license, the MAP program and all simulated datasets can be freely available at http://bioinfo.ctb.pku.edu.cn/MAP/
Binbin Lai, Ruogu Ding, Liping Duan, Huaiqiu Zhu
Bioinform.2