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Steven J. Rysavy

dblp:142/5352 · DBLP profile ↗
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2ranked-venue papers
1as first author
0since 2021 · last 2014
0000-0003-0211-9593ORCID · corroborated

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

Artificial intelligence and machine learning · 1 · 1 first-authorGraphics, computer vision, multimedia, augmented reality and games · 1 · 1 first-authorApplied, 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.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Computational science and engineering · 81% Bioinformatics and computational biology · 19%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Computational science and engineering
scientific visualization
0.212014
DIVE: a data intensive visualization engine · Bioinform. 2014
Computational science and engineering › computational chemistry › molecular simulation
molecular dynamics
0.112014
DIVE: a data intensive visualization engine · Bioinform. 2014
Bioinformatics and computational biology › protein dynamics
protein dynamics analysis
0.112014
DIVE: a data intensive visualization engine · Bioinform. 2014

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

data-intensive visualization · 0.2
YearPublicationVenuePosition
2014 DIVE: a data intensive visualization engine
abstract
Abstract Summary: Modern scientific investigation is generating increasingly larger datasets, yet analyzing these data with current tools is challenging. DIVE is a software framework intended to facilitate big data analysis and reduce the time to scientific insight. Here, we present features of the framework and demonstrate DIVE’s application to the Dynameomics project, looking specifically at two proteins. Availability and implementation: Binaries and documentation are available at http://www.dynameomics.org/DIVE/DIVESetup.exe. Contact: [email protected] Supplementary information: Supplementary data are available at Bioinformatics online.
Dennis Bromley, Steven J. Rysavy, Robert Su, Rudesh D. Toofanny, Tom Schmidlin, Valerie Daggett
Bioinform.2
2008 Classifiability criteria for refining of random walks segmentation
abstract
This paper proposes a novel approach to improve the segmentation quality of a 3D random walks algorithm using classifiability criteria. We produce a range of potential threshold values by extending the decision function of a random walks algorithm using a likelihood ratio test. Optimal threshold values are quantitatively isolated using two data-driven methods: maximum total accuracy and Bayesian cross validation criteria. The proposed methods are evaluated using a dataset of 28 dental lesions in 3D cone-beam CT scans. Both methods produce viable thresholds, the first corresponding to a conservative segmentation and the second a relaxed segmentation. We qualitatively compare the results to determine the best method.
Steven J. Rysavy, Arturo Flores, Reyes Enciso, Kazunori Okada
ICPR1