17 research outputs found

    Male and female survival under three artificial light sources: 1) light-emitting diode (LED, green); 2) fluorescent lamp (FL, blue); and 3) halogen lamp (HL, amber) during the 15 days for Experiment 1 [a], Experiment 2 [b], and Experiment 3 [c].

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    <p>Male and female survival under three artificial light sources: 1) light-emitting diode (LED, green); 2) fluorescent lamp (FL, blue); and 3) halogen lamp (HL, amber) during the 15 days for Experiment 1 [a], Experiment 2 [b], and Experiment 3 [c].</p

    Light spectra (μmol m<sup>-2</sup> s<sup>-1</sup>) of three artificial light sources: 1) light-emitting diode (LED, green); 2) fluorescent lamp (FL, blue); and 3) halogen lamp (HL, amber) at wavelengths from 300 to 885 nm.

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    <p>Light spectra (μmol m<sup>-2</sup> s<sup>-1</sup>) of three artificial light sources: 1) light-emitting diode (LED, green); 2) fluorescent lamp (FL, blue); and 3) halogen lamp (HL, amber) at wavelengths from 300 to 885 nm.</p

    S1 Appendix -

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    Identification and quantitative segmentation of individual blood vessels in mice visualized with preclinical imaging techniques is a tedious, manual or semiautomated task that can require weeks of reviewing hundreds of levels of individual data sets. Preclinical imaging, such as micro-magnetic resonance imaging (μMRI) can produce tomographic datasets of murine vasculature across length scales and organs, which is of outmost importance to study tumor progression, angiogenesis, or vascular risk factors for diseases such as Alzheimer’s. Training a neural network capable of accurate segmentation results requires a sufficiently large amount of labelled data, which takes a long time to compile. Recently, several reasonably automated approaches have emerged in the preclinical context but still require significant manual input and are less accurate than the deep learning approach presented in this paper—quantified by the Dice score. In this work, the implementation of a shallow, three-dimensional U-Net architecture for the segmentation of vessels in murine brains is presented, which is (1) open-source, (2) can be achieved with a small dataset (in this work only 8 μMRI imaging stacks of mouse brains were available), and (3) requires only a small subset of labelled training data. The presented model is evaluated together with two post-processing methodologies using a cross-validation, which results in an average Dice score of 61.34% in its best setup. The results show, that the methodology is able to detect blood vessels faster and more reliably compared to state-of-the-art vesselness filters with an average Dice score of 43.88% for the used dataset.</div

    Fig 2 -

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    The eight mice image stacks of the dataset showing the wild type mice in (a) to (d) and the knockout types in (e) to (h), each represented by one masked layer (l = 200) and the associated histogram. The first two images per row show brains of adult (a) (b) (e) (f) and the remaining two of young mice (c) (d) (g) (h). The histogram shows the percentage value distribution within the brain area of the whole stack.</p
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