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Ida Sundvor Opstad

dblp:272/0841 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2020
—ORCID · none

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

Artificial intelligence and machine learning · 1Graphics, computer vision, multimedia, augmented reality and games · 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.

Artificial intelligence
1 paper
Video understanding and tracking · 77% 3D vision · 23%
Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 2 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Computer vision › Video understanding and tracking › motion analysis
motion pattern analysis
0.412020
Learning Nanoscale Motion Patterns of Vesicles in Living Cells · CVPR 2020
Bioinformatics and computational biology › bioimage informatics
bioimage analysis
0.412020
Learning Nanoscale Motion Patterns of Vesicles in Living Cells · CVPR 2020

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

shallow residual attention network · 0.9physics-based simulation · 0.9nanoscopy · 0.9
YearPublicationVenuePosition
2020 Learning Nanoscale Motion Patterns of Vesicles in Living Cells
abstract
Detecting and analyzing nanoscale motion patterns of vesicles, smaller than the microscope resolution (~250 nm), inside living biological cells is a challenging problem. State-of-the-art CV approaches based on detection, tracking, optical flow or deep learning perform poorly for this problem. We propose an integrative approach, built upon physics based simulations, nanoscopy algorithms, and shallow residual attention network to make it possible for the first time to analysis sub-resolution motion patterns in vesicles that may also be of sub-resolution diameter. Our results show state-of-the-art performance, 89% validation accuracy on simulated dataset and 82% testing accuracy on an experimental dataset of living heart muscle cells imaged under three different pathological conditions. We demonstrate automated analysis of the motion states and changed in them for over 9000 vesicles. Such analysis will enable large scale biological studies of vesicle transport and interaction in living cells in the future.
Arif Ahmed 0002, Ida Sundvor Opstad, Åsa Birna Birgisdottir, Truls Myrmel, Balpreet Singh Ahluwalia, Krishna Agarwal, Dilip K. Prasad
CVPR2