Nuclear instance segmentation and tracking for preimplantation mouse embryos.

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Development Pub Date : 2024-11-01 Epub Date: 2024-11-06 DOI:10.1242/dev.202817
Hayden Nunley, Binglun Shao, David Denberg, Prateek Grover, Jaspreet Singh, Maria Avdeeva, Bradley Joyce, Rebecca Kim-Yip, Abraham Kohrman, Abhishek Biswas, Aaron Watters, Zsombor Gal, Alison Kickuth, Madeleine Chalifoux, Stanislav Y Shvartsman, Lisa M Brown, Eszter Posfai
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Abstract

For investigations into fate specification and morphogenesis in time-lapse images of preimplantation embryos, automated 3D instance segmentation and tracking of nuclei are invaluable. Low signal-to-noise ratio, high voxel anisotropy, high nuclear density, and variable nuclear shapes can limit the performance of segmentation methods, while tracking is complicated by cell divisions, low frame rates, and sample movements. Supervised machine learning approaches can radically improve segmentation accuracy and enable easier tracking, but they often require large amounts of annotated 3D data. Here, we first report a previously unreported mouse line expressing near-infrared nuclear reporter H2B-miRFP720. We then generate a dataset (termed BlastoSPIM) of 3D images of H2B-miRFP720-expressing embryos with ground truth for nuclear instances. Using BlastoSPIM, we benchmark seven convolutional neural networks and identify Stardist-3D as the most accurate instance segmentation method. With our BlastoSPIM-trained Stardist-3D models, we construct a complete pipeline for nuclear instance segmentation and lineage tracking from the eight-cell stage to the end of preimplantation development (>100 nuclei). Finally, we demonstrate the usefulness of BlastoSPIM as pre-train data for related problems, both for a different imaging modality and for different model systems.

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植入前小鼠胚胎的核实例分割和跟踪。
要研究植入前胚胎延时图像中的命运规范和形态发生,核的自动三维实例分割和跟踪非常重要。低信噪比、高体素各向异性、高核密度和多变的核形状会限制分割方法的性能,而细胞分裂、低帧频和样本移动又会使跟踪变得复杂。有监督的机器学习方法可以从根本上提高分割的准确性,并使追踪变得更容易,但它们通常需要大量的注释三维数据。在这里,我们首先报告了一种表达近红外核报告基因 H2B-miRFP720 的新型小鼠品系。然后,我们生成了一个数据集(称为 BlastoSPIM),该数据集包含表达 H2B-miRFP720 胚胎的三维图像和核实例的地面实况。利用 BlastoSPIM,我们对七个卷积神经网络进行了基准测试,发现 Stardist-3D 是最准确的实例分割方法。利用 BlastoSPIM 训练的 Stardist-3D 模型,我们构建了一个完整的核实例分割和谱系跟踪管道,可用于从 8 细胞阶段到植入前发育末期(>100 个细胞核)的核实例分割和谱系跟踪。最后,我们展示了 BlastoSPIM 作为相关问题的预训练数据的实用性,既适用于不同的成像模式,也适用于不同的模型系统。
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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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