Demo Data from SIGIR 2026 / reviewers in the wild / expert
Truls Myrmel
dblp:272/0607
· DBLP profile ↗
1ranked-venue papers
0as first author
0since 2021 · last 2020
—ORCID · unresolved
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
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Computer vision › Video understanding and tracking › motion analysis
motion pattern analysis |
0.4 | 1 | 2020 | Learning Nanoscale Motion Patterns of Vesicles in Living Cells · CVPR 2020 |
Bioinformatics and computational biology › bioimage informatics
bioimage analysis |
0.4 | 1 | 2020 | 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
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2020 | Learning Nanoscale Motion Patterns of Vesicles in Living CellsabstractDetecting 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 |
CVPR | 4 |