Nature BiotechnologyBioinformaticsPeer-reviewed journal article
Whole-cell segmentation of tissue images with human-level performance using large-scale data annotation and deep learning
Noah F. GreenwaldiD, Geneva MilleriD, Erick MoeniD, Alex KongiD, Adam Kagel, Thomas DoughertyiD, Christine Camacho FullawayiD, Brianna J. McIntoshiD, Ke Xuan Leow, Morgan Sarah SchwartziD, Cole PavelchekiD, Sunny CuiiD, Isabella CamplissoniD, Omer Bar-TaliD, Jaiveer SinghiD, Mara Fong, Gautam ChaudhryiD, Zion Abraham, Jackson Moseley, Shiri Warshawsky, Erin SooniD, Shirley GreenbaumiD, Tyler RisomiD, Travis J. HollmanniD, Sean C. BendalliD, , David Van ValeniD
Abstract
Understanding the spatial organization of tissues is of critical importance for both basic and translational research. While recent advances in tissue imaging are opening an exciting new window into the biology of human tissues, interpreting the data that they create is a significant computational challenge. Cell segmentation, the task of uniquely identifying each cell in an image, remains a substantial barrier for tissue imaging, as existing approaches are inaccurate or require a substantial amount of manual curation to yield useful results. Here, we addressed the problem of cell segmentation in tissue imaging data through large-scale data annotation and deep learning. We constructed TissueNet, an image dataset containing >1 million paired whole-cell and nuclear annotations for tissue images from nine organs and six imaging platforms. We created Mesmer, a deep learning-enabled segmentation algorithm trained on TissueNet that performs nuclear and whole-cell segmentation in tissue imaging data. We demonstrated that Mesmer has better speed and accuracy than previous methods, generalizes to the full diversity of tissue types and imaging platforms in TissueNet, and achieves human-level performance for whole-cell segmentation. Mesmer enabled the automated extraction of key cellular features, such as subcellular localization of protein signal, which was challenging with previous approaches. We further showed that Mesmer could be adapted to harness cell lineage information present in highly multiplexed datasets. We used this enhanced version to quantify cell morphology changes during human gestation. All underlying code and models are released with permissive licenses as a community resource.
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- top 1%
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