Democratising deep learning for microscopy with ZeroCostDL4Mic

Lucas von Chamier(MRC Laboratory for Molecular Cell Biology), Romain F. Laine(The Francis Crick Institute), Johanna Jukkala(Åbo Akademi University), Christoph Spahn(Goethe University Frankfurt), Daniel Krentzel(The Francis Crick Institute), Elias Nehme(Technion – Israel Institute of Technology), Martina Lerche(Åbo Akademi University), Sara Hernández‐Pérez(Åbo Akademi University), Pieta K. Mattila(Åbo Akademi University), Eleni Karinou(Newcastle University), Séamus Holden(Newcastle University), Ahmet Can Solak(Chan Zuckerberg Initiative (United States)), Alexander Krull(Max Planck Institute for Physics), Tim-Oliver Buchholz(Center for Systems Biology Dresden), Martin L. Jones(The Francis Crick Institute), Löıc A. Royer(Chan Zuckerberg Initiative (United States)), Christophe Leterrier(Centre National de la Recherche Scientifique), Yoav Shechtman(Technion – Israel Institute of Technology), Florian Jug(Human Technopole), Mike Heilemann(Goethe University Frankfurt), Guillaume Jacquemet(Åbo Akademi University), Ricardo Henriques(The Francis Crick Institute)
Nature Communications
April 15, 2021
Cited by 554Open Access
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Abstract

Deep Learning (DL) methods are powerful analytical tools for microscopy and can outperform conventional image processing pipelines. Despite the enthusiasm and innovations fuelled by DL technology, the need to access powerful and compatible resources to train DL networks leads to an accessibility barrier that novice users often find difficult to overcome. Here, we present ZeroCostDL4Mic, an entry-level platform simplifying DL access by leveraging the free, cloud-based computational resources of Google Colab. ZeroCostDL4Mic allows researchers with no coding expertise to train and apply key DL networks to perform tasks including segmentation (using U-Net and StarDist), object detection (using YOLOv2), denoising (using CARE and Noise2Void), super-resolution microscopy (using Deep-STORM), and image-to-image translation (using Label-free prediction - fnet, pix2pix and CycleGAN). Importantly, we provide suitable quantitative tools for each network to evaluate model performance, allowing model optimisation. We demonstrate the application of the platform to study multiple biological processes.


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