Evidence map›Paper›PMID 32060319›Full record

ArticleScientific reports2020

Prediction of Sequential Organelles Localization under Imbalance using A Balanced Deep U-Net.

Novanto Yudistira, Muthusubash Kavitha, Takeshi Itabashi, Atsuko H Iwane, Takio Kurita

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Novanto YudistiraHiroshima University, Department of Information Engineering, Higashi Hiroshima, 739-8521, Japan. yudistira@ub.ac.id.
Muthusubash KavithaHiroshima University, Department of Information Engineering, Higashi Hiroshima, 739-8521, Japan.
Takeshi ItabashiRiken, Center for Biosystems Dynamics Research, Laboratory for Cell Field Structure, Higashi Hiroshima, 739-0046, Japan.
Atsuko H IwaneRiken, Center for Biosystems Dynamics Research, Laboratory for Cell Field Structure, Higashi Hiroshima, 739-0046, Japan.
Takio KuritaHiroshima University, Department of Information Engineering, Higashi Hiroshima, 739-8521, Japan.
Hiroshima University · JPRIKEN Center for Biosystems Dynamics Research · JPUbe Frontier University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Assessing the structure and function of organelles in living organisms of the primitive unicellular red algae Cyanidioschyzon merolae on three-dimensional sequential images demands a reliable automated technique in the class imbalance among various cellular structures during mitosis. Existing classification networks with commonly used loss functions were focused on larger numbers of cellular structures that lead to the unreliability of the system. Hence, we proposed a balanced deep regularized weighted compound dice loss (RWCDL) network for better localization of cell organelles. Specifically, we introduced two new loss functions, namely compound dice (CD) and RWCD by implementing multi-class variant dice and weighting mechanism, respectively for maximizing weights of peroxisome and nucleus among five classes as the main contribution of this study. We extended the Unet-like convolution neural network (CNN) architecture for evaluating the ability of our proposed loss functions for improved segmentation. The feasibility of the proposed approach is confirmed with three different large scale mitotic cycle data set with different number of occurrences of cell organelles. In addition, we compared the training behavior of our designed architectures with the ground truth segmentation using various performance measures. The proposed balanced RWCDL network generated the highest area under the curve (AUC) value in elevating the small and obscure peroxisome and nucleus, which is 30% higher than the network with commonly used mean square error (MSE) and dice loss (DL) functions. The experimental results indicated that the proposed approach can efficiently identify the cellular structures, even when the contour between the cells is obscure and thus convinced that the balanced deep RWCDL approach is reliable and can be helpful for biologist to accurately identify the relationship between the cell behavior and structures of cell organelles during mitosis.

Indexed as

Neural Networks, ComputerAlgorithmsImage Processing, Computer-AssistedImaging, Three-DimensionalMicroscopy, Electron, ScanningMitosisOrganellesRhodophyta

Identifiers

PMID32060319
PMCPMC7021757
OpenAlexW3006618770

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.