Evidence map›Paper›PMID 30767778›Full record

ArticleBMC bioinformatics2019

Iterative unsupervised domain adaptation for generalized cell detection from brightfield z-stacks.

Kaisa Liimatainen, Lauri Kananen, Leena Latonen, Pekka Ruusuvuori

Abstract read
In one paragraph

Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Low-Resource Adversarial Domain Adaptation for Cross-Modality Nucleus Detection.Medical image computing and computer-assisted intervention : MICCAI ... International Conference on Medical Image Computing and Computer-Assisted Intervention · 2022
    Article
  2. Article
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

4 authors.

Kaisa LiimatainenFaculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Lauri KananenFaculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Leena LatonenFaculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Pekka RuusuvuoriFaculty of Medicine and Health Technology, Tampere University, Tampere, Finland. pekka.ruusuvuori@tuni.fi.ORCID http://orcid.org/0000-0001-9086-9591

Funding

Academy of Finland 313921Academy of Finland 314558Academy of Finland 317871
6 · The paper itself

Abstract

backgroundCell counting from cell cultures is required in multiple biological and biomedical research applications. Especially, accurate brightfield-based cell counting methods are needed for cell growth analysis. With deep learning, cells can be detected with high accuracy, but manually annotated training data is required. We propose a method for cell detection that requires annotated training data for one cell line only, and generalizes to other, unseen cell lines.

resultsTraining a deep learning model with one cell line only can provide accurate detections for similar unseen cell lines (domains). However, if the new domain is very dissimilar from training domain, high precision but lower recall is achieved. Generalization capabilities of the model can be improved with training data transformations, but only to a certain degree. To further improve the detection accuracy of unseen domains, we propose iterative unsupervised domain adaptation method. Predictions of unseen cell lines with high precision enable automatic generation of training data, which is used to train the model together with parts of the previously used annotated training data. We used U-Net-based model, and three consecutive focal planes from brightfield image z-stacks. We trained the model initially with PC-3 cell line, and used LNCaP, BT-474 and 22Rv1 cell lines as target domains for domain adaptation. Highest improvement in accuracy was achieved for 22Rv1 cells. F

conclusionsWith our method for generalized cell detection, we can train a model that accurately detects different cell lines from brightfield images. A new cell line can be introduced to the model without a single manual annotation, and after iterative domain adaptation the model is ready to detect these cells with high accuracy.

Indexed as

Deep LearningHumansImage Processing, Computer-AssistedMaleProstatic NeoplasmsTumor Cells, CulturedBrightfieldCell detectionDeep learningSemi-supervised learningUnsupervised domain adaptation

Identifiers

PMID30767778
PMCPMC6376647

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.