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nucleAIzer: A Parameter-free Deep Learning Framework for Nucleus Segmentation Using Image Style Transfer.
Hollandi, Reka; Szkalisity, Abel; Toth, Timea; Tasnadi, Ervin; Molnar, Csaba; Mathe, Botond; Grexa, Istvan; Molnar, Jozsef; Balind, Arpad; Gorbe, Mate; Kovacs, Maria; Migh, Ede; Goodman, Allen; Balassa, Tamas; Koos, Krisztian; Wang, Wenyu; Caicedo, Juan Carlos; Bara, Norbert; Kovacs, Ferenc; Paavolainen, Lassi; Danka, Tivadar; Kriston, Andras; Carpenter, Anne Elizabeth; Smith, Kevin; Horvath, Peter.
Afiliação
  • Hollandi R; Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Szkalisity A; Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Toth T; Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Tasnadi E; Doctoral School of Biology, University of Szeged, Közép fasor 52, Szeged 6726, Hungary.
  • Molnar C; Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Mathe B; Doctoral School of Computer Science, University of Szeged,Árpád tér 2, Szeged 6720, Hungary.
  • Grexa I; Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Molnar J; Doctoral School of Computer Science, University of Szeged,Árpád tér 2, Szeged 6720, Hungary.
  • Balind A; Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Gorbe M; Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Kovacs M; Doctoral School of Interdisciplinary Medicine, University of Szeged, Koranyi fasor 10, Szeged 6720, Hungary.
  • Migh E; Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Goodman A; Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Balassa T; Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Koos K; Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Wang W; Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Caicedo JC; Imaging Platform, Broad Institute of Harvard and MIT, 415 Main Street, Cambridge, MA 02142, USA.
  • Bara N; Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Kovacs F; Doctoral School of Informatics, Eötvös Loránd University, Pázmány Péter sétány 1/C, Room 2.317, Budapest 1117, Hungary.
  • Paavolainen L; Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Danka T; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Tukholmankatu 8, Helsinki 00014, Finland.
  • Kriston A; Imaging Platform, Broad Institute of Harvard and MIT, 415 Main Street, Cambridge, MA 02142, USA.
  • Carpenter AE; Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Smith K; Single-Cell Technologies Ltd, Szeged 6726, Hungary.
  • Horvath P; Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
Cell Syst ; 10(5): 453-458.e6, 2020 05 20.
Article em En | MEDLINE | ID: mdl-34222682
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article