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Ellen T. Arena

dblp:210/8953 · DBLP profile ↗
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3ranked-venue papers
0as first author
0since 2021 · last 2019
0000-0002-1049-9971ORCID · corroborated

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

Graphics, computer vision, multimedia, augmented reality and games · 2Applied, 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
2 papers
Bioinformatics and computational biology · 100%

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › bioimage informatics › bioimage analysis › microscopy image analysis
colocalization analysis
0.722019
Spatially Adaptive Colocalization Analysis in Dual-Color Fluorescence Microscopy · IEEE Trans. Image Process. 2019
Automated and Robust Quantification of Colocalization in Dual-Color Fluorescence Microscopy: A Nonparametric Statistical Approach · IEEE Trans. Image Process. 2018
Bioinformatics and computational biology › bioimage informatics › bioimage analysis
microscopy image analysis
0.722019
Spatially Adaptive Colocalization Analysis in Dual-Color Fluorescence Microscopy · IEEE Trans. Image Process. 2019
Automated and Robust Quantification of Colocalization in Dual-Color Fluorescence Microscopy: A Nonparametric Statistical Approach · IEEE Trans. Image Process. 2018
Bioinformatics and computational biology › bioimage informatics › bioimage analysis › microscopy image analysis
fluorescence microscopy
0.222019
Spatially Adaptive Colocalization Analysis in Dual-Color Fluorescence Microscopy · IEEE Trans. Image Process. 2019
Automated and Robust Quantification of Colocalization in Dual-Color Fluorescence Microscopy: A Nonparametric Statistical Approach · IEEE Trans. Image Process. 2018

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

spatial statistics · 0.4propagation-separation · 0.4local kernel model · 0.4statistical testing · 0.3scan statistics · 0.3non-parametric statistics · 0.3
YearPublicationVenuePosition
2019 Spatially Adaptive Colocalization Analysis in Dual-Color Fluorescence Microscopy
abstract
Colocalization analysis aims to study complex spatial associations between bio-molecules via optical imaging techniques. However, existing colocalization analysis workflows only assess an average degree of colocalization within a certain region of interest and ignore the unique and valuable spatial information offered by microscopy. In the current work, we introduce a new framework for colocalization analysis that allows us to quantify colocalization levels at each individual location and automatically identify pixels or regions where colocalization occurs. The framework, referred to as spatially adaptive colocalization analysis (SACA), integrates a pixel-wise local kernel model for colocalization quantification and a multi-scale adaptive propagation-separation strategy for utilizing spatial information to detect colocalization in a spatially adaptive fashion. Applications to simulated and real biological datasets demonstrate the practical merits of SACA in what we hope to be an easily applicable and robust colocalization analysis method. In addition, theoretical properties of SACA are investigated to provide rigorous statistical justification.
Shulei Wang, Ellen T. Arena, Jordan T. Becker, William M. Bement, Nathan M. Sherer, Kevin W. Eliceiri, Ming Yuan 0001
IEEE Trans. Image Process.2
2018 Automated and Robust Quantification of Colocalization in Dual-Color Fluorescence Microscopy: A Nonparametric Statistical Approach
abstract
Colocalization is a powerful tool to study the interactions between fluorescently labeled molecules in biological fluorescence microscopy. However, existing techniques for colocalization analysis have not undergone continued development especially in regards to robust statistical support. In this paper, we examine two of the most popular quantification techniques for colocalization and argue that they could be improved upon using ideas from nonparametric statistics and scan statistics. In particular, we propose a new colocalization metric that is robust, easily implementable, and optimal in a rigorous statistical testing framework. Application to several benchmark data sets, as well as biological examples, further demonstrates the usefulness of the proposed technique.
Shulei Wang, Ellen T. Arena, Kevin W. Eliceiri, Ming Yuan 0001
IEEE Trans. Image Process.2
2017 ImageJ2: ImageJ for the next generation of scientific image data
abstract
BACKGROUND: ImageJ is an image analysis program extensively used in the biological sciences and beyond. Due to its ease of use, recordable macro language, and extensible plug-in architecture, ImageJ enjoys contributions from non-programmers, amateur programmers, and professional developers alike. Enabling such a diversity of contributors has resulted in a large community that spans the biological and physical sciences. However, a rapidly growing user base, diverging plugin suites, and technical limitations have revealed a clear need for a concerted software engineering effort to support emerging imaging paradigms, to ensure the software's ability to handle the requirements of modern science. RESULTS: We rewrote the entire ImageJ codebase, engineering a redesigned plugin mechanism intended to facilitate extensibility at every level, with the goal of creating a more powerful tool that continues to serve the existing community while addressing a wider range of scientific requirements. This next-generation ImageJ, called "ImageJ2" in places where the distinction matters, provides a host of new functionality. It separates concerns, fully decoupling the data model from the user interface. It emphasizes integration with external applications to maximize interoperability. Its robust new plugin framework allows everything from image formats, to scripting languages, to visualization to be extended by the community. The redesigned data model supports arbitrarily large, N-dimensional datasets, which are increasingly common in modern image acquisition. Despite the scope of these changes, backwards compatibility is maintained such that this new functionality can be seamlessly integrated with the classic ImageJ interface, allowing users and developers to migrate to these new methods at their own pace. CONCLUSIONS: Scientific imaging benefits from open-source programs that advance new method development and deployment to a diverse audience. ImageJ has continuously evolved with this idea in mind; however, new and emerging scientific requirements have posed corresponding challenges for ImageJ's development. The described improvements provide a framework engineered for flexibility, intended to support these requirements as well as accommodate future needs. Future efforts will focus on implementing new algorithms in this framework and expanding collaborations with other popular scientific software suites.
Curtis Rueden, Johannes E. Schindelin, Mark C. Hiner, Barry E. DeZonia, Alison E. Walter, Ellen T. Arena, Kevin W. Eliceiri
BMC Bioinform.6