Deep Reinforcement Learning Based Progressive Sequence Saliency Discovery Network for Mitosis Detection In Time-Lapse Phase-Contrast Microscopy Images.
Clicks: 382
ID: 110430
2020
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This
article has not been analysed, so there is no overall score —
reader engagement is measured and shown alongside.
Reader Engagement
Emerging Content
30.0
/100
382 views
39 readers
AI Quality Assessment
Not analyzed
Readership in this journal
EmergingRanked #5 of 27 articles by views in ieee/acm transactions on computational biology and bioinformatics
Most read
Least read
Bar heights use a square-root scale.
Mint this article as an NFT
Not yet mintedCreate a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.
5
SUSD
one-off · no wallet required
Abstract
In this paper, we propose a deep reinforcement learning-based progressive sequence saliency discovery network (PSSD) for mitosis detection in time-lapse phase contrast microscopy images. The proposed method consists of two parts: 1) the saliency discovery module that selects the salient frames from the input cell image sequence by progressively adjusting the selection positions of salient frames; 2) the mitosis identification module that takes a sequence of salient frames and performs temporal information fusion for mitotic sequence classification. Since the policy network of the saliency discovery module is trained under the guidance of the mitosis identification module, PSSD can comprehensively explore the salient frames that are beneficial for mitosis detection. To our knowledge, this is the first work to implement deep reinforcement learning to the mitosis detection problem. In the experiment, we evaluate the proposed method on the largest mitosis detection dataset, C2C12-16. Experiment results show that compared with the state of the arts, the proposed method can achieve significant improvement for both mitosis identification and temporal localization on C2C12.
| Reference Key |
su2020deepieeeacm
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | Su, Yuting;Lu, Yao;Chen, Mei;Liu, An-An; |
| Journal | ieee/acm transactions on computational biology and bioinformatics |
| Year | 2020 |
| DOI |
10.1109/TCBB.2020.3019042
|
| URL | |
| Keywords |
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.