| Literature DB >> 29656897 |
Eric M Christiansen1, Samuel J Yang2, D Michael Ando2, Ashkan Javaherian3, Gaia Skibinski3, Scott Lipnick4, Elliot Mount3, Alison O'Neil5, Kevan Shah3, Alicia K Lee3, Piyush Goyal3, William Fedus6, Ryan Poplin2, Andre Esteva7, Marc Berndl2, Lee L Rubin5, Philip Nelson8, Steven Finkbeiner9.
Abstract
Microscopy is a central method in life sciences. Many popular methods, such as antibody labeling, are used to add physical fluorescent labels to specific cellular constituents. However, these approaches have significant drawbacks, including inconsistency; limitations in the number of simultaneous labels because of spectral overlap; and necessary perturbations of the experiment, such as fixing the cells, to generate the measurement. Here, we show that a computational machine-learning approach, which we call "in silico labeling" (ISL), reliably predicts some fluorescent labels from transmitted-light images of unlabeled fixed or live biological samples. ISL predicts a range of labels, such as those for nuclei, cell type (e.g., neural), and cell state (e.g., cell death). Because prediction happens in silico, the method is consistent, is not limited by spectral overlap, and does not disturb the experiment. ISL generates biological measurements that would otherwise be problematic or impossible to acquire.Entities:
Keywords: cancer; computer vision; deep learning; machine learning; microscopy; neuroscience; stem cells
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Year: 2018 PMID: 29656897 PMCID: PMC6309178 DOI: 10.1016/j.cell.2018.03.040
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582