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CLANet: A comprehensive framework for cross-batch cell line identification using brightfield images.
Tong, Lei; Corrigan, Adam; Kumar, Navin Rathna; Hallbrook, Kerry; Orme, Jonathan; Wang, Yinhai; Zhou, Huiyu.
Affiliation
  • Tong L; School of Computing and Mathematical Sciences, University of Leicester, Leicester, UK; Data Sciences and Quantitative Biology, Discovery Sciences, AstraZeneca R&D, Cambridge, UK.
  • Corrigan A; Data Sciences and Quantitative Biology, Discovery Sciences, AstraZeneca R&D, Cambridge, UK.
  • Kumar NR; UK Cell Culture and Banking, Discovery Sciences, AstraZeneca R&D, Alderley Park, UK.
  • Hallbrook K; UK Cell Culture and Banking, Discovery Sciences, AstraZeneca R&D, Alderley Park, UK.
  • Orme J; UK Cell Culture and Banking, Discovery Sciences, AstraZeneca R&D, Cambridge, UK.
  • Wang Y; Data Sciences and Quantitative Biology, Discovery Sciences, AstraZeneca R&D, Cambridge, UK. Electronic address: yinhai.wang@astrazeneca.com.
  • Zhou H; School of Computing and Mathematical Sciences, University of Leicester, Leicester, UK. Electronic address: hz143@leicester.ac.uk.
Med Image Anal ; 94: 103123, 2024 May.
Article in En | MEDLINE | ID: mdl-38430651
ABSTRACT
Cell line authentication plays a crucial role in the biomedical field, ensuring researchers work with accurately identified cells. Supervised deep learning has made remarkable strides in cell line identification by studying cell morphological features through cell imaging. However, biological batch (bio-batch) effects, a significant issue stemming from the different times at which data is generated, lead to substantial shifts in the underlying data distribution, thus complicating reliable differentiation between cell lines from distinct batch cultures. To address this challenge, we introduce CLANet, a pioneering framework for cross-batch cell line identification using brightfield images, specifically designed to tackle three distinct bio-batch effects. We propose a cell cluster-level selection method to efficiently capture cell density variations, and a self-supervised learning strategy to manage image quality variations, thus producing reliable patch representations. Additionally, we adopt multiple instance learning(MIL) for effective aggregation of instance-level features for cell line identification. Our innovative time-series segment sampling module further enhances MIL's feature-learning capabilities, mitigating biases from varying incubation times across batches. We validate CLANet using data from 32 cell lines across 93 experimental bio-batches from the AstraZeneca Global Cell Bank. Our results show that CLANet outperforms related approaches (e.g. domain adaptation, MIL), demonstrating its effectiveness in addressing bio-batch effects in cell line identification.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Line Authentication Limits: Humans Language: En Journal: Med Image Anal Journal subject: DIAGNOSTICO POR IMAGEM Year: 2024 Type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Line Authentication Limits: Humans Language: En Journal: Med Image Anal Journal subject: DIAGNOSTICO POR IMAGEM Year: 2024 Type: Article Affiliation country: United kingdom