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Noel F. C. C. de Miranda

dblp:267/1773 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2021
0000-0001-6122-1024ORCID · verified

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

Graphics, computer vision, multimedia, augmented reality and games · 1 · 1 since 2021

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
Bioinformatics and computational biology · 100%
Computer graphics and multimedia
1 paper
Visualization and visual analytics · 100%

Topics — the 5 heaviest of 5, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › single-cell analysis
single-cell omics
0.512021
Visual cohort comparison for spatial single-cell omics-data · IEEE Trans. Vis. Comput. Graph. 2021
Bioinformatics and computational biology › omics data analysis
spatial omics
0.512021
Visual cohort comparison for spatial single-cell omics-data · IEEE Trans. Vis. Comput. Graph. 2021
Visualization and visual analytics › medical visualization
cohort comparison
0.512021
Visual cohort comparison for spatial single-cell omics-data · IEEE Trans. Vis. Comput. Graph. 2021
Visualization and visual analytics
visual analytics
0.512021
Visual cohort comparison for spatial single-cell omics-data · IEEE Trans. Vis. Comput. Graph. 2021
Bioinformatics and computational biology
biomarker discovery
0.112021
Visual cohort comparison for spatial single-cell omics-data · IEEE Trans. Vis. Comput. Graph. 2021

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

interactive visual analysis · 1.0co-localization analysis · 1.0
YearPublicationVenuePosition
2021 Visual cohort comparison for spatial single-cell omics-data
abstract
Spatially-resolved omics-data enable researchers to precisely distinguish cell types in tissue and explore their spatial interactions, enabling deep understanding of tissue functionality. To understand what causes or deteriorates a disease and identify related biomarkers, clinical researchers regularly perform large-scale cohort studies, requiring the comparison of such data at cellular level. In such studies, with little a-priori knowledge of what to expect in the data, explorative data analysis is a necessity. Here, we present an interactive visual analysis workflow for the comparison of cohorts of spatially-resolved omics-data. Our workflow allows the comparative analysis of two cohorts based on multiple levels-of-detail, from simple abundance of contained cell types over complex co-localization patterns to individual comparison of complete tissue images. As a result, the workflow enables the identification of cohort-differentiating features, as well as outlier samples at any stage of the workflow. During the development of the workflow, we continuously consulted with domain experts. To show the effectiveness of the workflow, we conducted multiple case studies with domain experts from different application areas and with different data modalities.
Antonios Somarakis, Marieke E. Ijsselsteijn, Sietse J. Luk, Boyd Kenkhuis, Noel F. C. C. de Miranda, Boudewijn P. F. Lelieveldt, Thomas Höllt
IEEE Trans. Vis. Comput. Graph.5