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    <meta name="description" content="New Results - Image restoration, manipulation and enhancement"/>
    <meta name="dc.title" content="New Results - Image restoration, manipulation and enhancement"/>
    <meta name="dc.creator" content="Anton Osokin"/>
    <meta name="dc.creator" content="Anatole Chessel"/>
    <meta name="dc.creator" content="Rafael E. Carazo Salas"/>
    <meta name="dc.creator" content="Federico Vaggi"/>
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    <meta name="dc.date" content="(SCHEME=ISO8601) 2017-01"/>
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      <div class="TdmEntry">Overall Objectives<ul><li><a href="./uid3.html">Statement</a></li></ul></div>
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	    Raweb 
	    2017</a> | <a href="http://www.inria.fr/en/teams/willow">Presentation of the Project-Team WILLOW</a> | <a href="http://www.di.ens.fr/willow">WILLOW Web Site
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        <h2>Section: 
      New Results</h2>
        <h3 class="titre3">Image restoration, manipulation and enhancement</h3>
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        <h4 class="titre4">GANs for Biological Image Synthesis</h4>
        <p class="participants"><span class="part">Participants</span> :
	Anton Osokin, Anatole Chessel, Rafael E. Carazo Salas, Federico Vaggi.</p>
        <p>In this work we propose a novel application of Generative Adversarial Networks (GAN) to the synthesis of cells imaged by fluorescence microscopy. Compared to natural images, cells tend to have a simpler and more geometric global structure that facilitates image generation. However, the correlation between the spatial pattern of different fluorescent proteins reflects important biological functions, and synthesized images have to capture these relationships to be relevant for biological applications. We adapt GANs to the task at hand and propose new models with casual dependencies between image channels that can generate multi-channel images, which would be impossible to obtain experimentally (see Figure <a title="Image restoration, manipulation and enhancement" href="./uid88.html#uid90">9</a>). We evaluate our approach using two independent techniques and compare it against sensible baselines. Finally, we demonstrate that by interpolating across the latent space we can mimic the known changes in protein localization that occur through time during the cell cycle, allowing us to predict temporal evolution from static images. This paper has been published in <a href="./bibliography.html#willow-2017-bid9">[17]</a>.</p>
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            <caption align="bottom"><strong>Figure
	9. </strong>Real (left) and generated (right) images of fission yeast cells with protein bgs4 depicted in the red channel and 6 other proteins depicted in the green channel.
The synthetic images were generated with our star-shaped GAN.
The star-shaped model can generate multiple green channels aligned with the same red channel whereas the training images have only one green channel.</caption>
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