Evidence map›Paper›PMID 34222682›Full record

ArticleCell systems2020

nucleAIzer: A Parameter-free Deep Learning Framework for Nucleus Segmentation Using Image Style Transfer.

Reka Hollandi, Abel Szkalisity, Timea Toth, Ervin Tasnadi, Csaba Molnar, Botond Mathe, Istvan Grexa, Jozsef Molnar, Arpad Balind, Mate Gorbe and 15 more

Abstract read
In one paragraph

Article in Cell systems, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 130 papers.

0numbers the graph read from it
0cells of the map it votes in
130citing 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

130 citing papers in PubMed.

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70 more citing papers are in PubMed but not listed here.

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

25 authors.

Reka HollandiSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Abel SzkalisitySynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Timea TothSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Ervin TasnadiSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Csaba MolnarSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Botond MatheSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Istvan GrexaSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Jozsef MolnarSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Arpad BalindSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Mate GorbeSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Maria KovacsSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Ede MighSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Allen GoodmanImaging Platform, Broad Institute of Harvard and MIT, 415 Main Street, Cambridge, MA 02142, USA.
Tamas BalassaSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Krisztian KoosSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Wenyu WangInstitute for Molecular Medicine Finland (FIMM), University of Helsinki, Tukholmankatu 8, Helsinki 00014, Finland.
Juan Carlos CaicedoImaging Platform, Broad Institute of Harvard and MIT, 415 Main Street, Cambridge, MA 02142, USA.
Norbert BaraSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Ferenc KovacsSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Lassi PaavolainenInstitute for Molecular Medicine Finland (FIMM), University of Helsinki, Tukholmankatu 8, Helsinki 00014, Finland.
Tivadar DankaSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Andras KristonSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Anne Elizabeth CarpenterImaging Platform, Broad Institute of Harvard and MIT, 415 Main Street, Cambridge, MA 02142, USA.
Kevin SmithKTH Royal Institute of Technology, School of Computer Science and Communication, Lindstedtsvägen 3, Stockholm 10044, Sweden.
Peter HorvathSynthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.

Funding

Extracting rich information from biological imagesR35GM122547 · NIGMS · BROAD INSTITUTE, INC. · PI Anne E. Carpenter · 2017 to 2026
$6.2M
NIGMS NIH HHS R35 GM122547
6 · The paper itself

Abstract

Single-cell segmentation is typically a crucial task of image-based cellular analysis. We present nucleAIzer, a deep-learning approach aiming toward a truly general method for localizing 2D cell nuclei across a diverse range of assays and light microscopy modalities. We outperform the 739 methods submitted to the 2018 Data Science Bowl on images representing a variety of realistic conditions, some of which were not represented in the training data. The key to our approach is that during training nucleAIzer automatically adapts its nucleus-style model to unseen and unlabeled data using image style transfer to automatically generate augmented training samples. This allows the model to recognize nuclei in new and different experiments efficiently without requiring expert annotations, making deep learning for nucleus segmentation fairly simple and labor free for most biological light microscopy experiments. It can also be used online, integrated into CellProfiler and freely downloaded at www.nucleaizer.org. A record of this paper's transparent peer review process is included in the Supplemental Information.

Indexed as

Cell NucleusDeep LearningMicroscopy

Identifiers

PMID34222682
PMCPMC8247631

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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.