Data from: OoCount: A machine-learning based approach to mouse ovarian follicle counting and classification
The number and distribution of ovarian follicles in each growth stage provides a reliable readout of ovarian health and function. Leveraging techniques for three-dimensional (3D) imaging of ovaries in toto has the potential to uncover total, accurate ovarian follicle counts. However, because of the...
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Zusammenfassung: | The number and distribution of ovarian follicles in each growth stage
provides a reliable readout of ovarian health and function. Leveraging
techniques for three-dimensional (3D) imaging of ovaries in toto has the
potential to uncover total, accurate ovarian follicle counts. However,
because of the size and holistic nature of these images, counting oocytes
is time consuming and difficult. The advent of deep-learning algorithms
has allowed for the rapid development of ultra-fast, automated methods to
analyze microscopy images. In recent years, these pipelines have become
more user-friendly and accessible to non-specialists. We used these tools
to create OoCount, a high-throughput, open-source method for automatic
oocyte segmentation and classification from fluorescent 3D microscopy
images of whole mouse ovaries using a deep-learning convolutional neural
network (CNN) based approach. We developed a fast clearing and spinning
disk confocal-based imaging protocol to obtain 3D images of whole mount
perinatal and adult mouse ovaries. Then, fluorescently labeled oocytes
from 3D images of ovaries were manually annotated to develop a machine
learning training dataset. This dataset was used to train a CNN to
automatically label all oocytes in the ovary. In a second phase, we
trained another CNN to classify labeled oocytes and sort them into growth
stages. Using OoCount, we can obtain accurate counts of oocytes in each
growth stage in the perinatal and adult ovary, improving our ability to
study ovarian function and fertility. Here, we provide an end-to-end
protocol for developing high quality 3D images of the perinatal and adult
mouse ovary, obtaining follicle counts and stages, and how to customize
OoCount to fit images produced in any lab. |
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DOI: | 10.5061/dryad.nk98sf81r |