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        <title>Learning Genetic interactions with Deep neural Networks</title>
        <description> The application of AI to biology is leading to revolutionary achievements with Alphafold for protein folding and generative models of artificial enzymes. However, a question remains open at a higher level of organization in cells, crucial for diagnosis and therapeutic strategies: how to predict the impact of multiple gene perturbations on biological functions? The aim of the project is to develop a deep learning approach leveraging on the one hand recent work on deep neural networks in the MILES team of Dauphine [1] and on the other hand experiments and mechanistic models developed at the ESPCI laboratory, showing that interactions between mutations are largely explained by non-linear but smooth functions of intermediate features [2-3]. How can we design a deep-learning model that can include these two steps of decomposition to learn gene interactions? 

For this purpose, the PhD will develop three complementary lines of research: (i) build deep nets on published datasets of combined genetic and drug perturbations on cells; (ii) computationally simulate the response of cells based on typical gene network architectures; (iii) apply the developed models to design, predict and interpret the outcome of large scale screening experiments done at ESPCI.

The PhD will be co-supervised by Alexandre Allauzen, Professor at University Paris Dauphine and ESPCI  (team Machine Intelligence and LEarning Systems) and Philippe Nghe (director of the Laboratory of Biophysics and Evolution, ESPCI Paris-PSL). It is funded by the CNRS. Possible profiles include former experience in deep learning, computational biology, physics, mathematics. The position is expected  to start around September 2022.
Contacts: &amp;#97;&amp;#108;&amp;#101;&amp;#120;&amp;#97;&amp;#110;&amp;#100;&amp;#114;&amp;#101;&amp;#46;&amp;#97;&amp;#108;&amp;#108;&amp;#97;&amp;#117;&amp;#122;&amp;#101;&amp;#110;&amp;#64;&amp;#100;&amp;#97;&amp;#117;&amp;#112;&amp;#104;&amp;#105;&amp;#110;&amp;#101;&amp;#46;&amp;#112;&amp;#115;&amp;#108;&amp;#46;&amp;#101;&amp;#117;;  &amp;#112;&amp;#104;&amp;#105;&amp;#108;&amp;#105;&amp;#112;&amp;#112;&amp;#101;&amp;#46;&amp;#110;&amp;#103;&amp;#104;&amp;#101;&amp;#64;&amp;#101;&amp;#115;&amp;#112;&amp;#99;&amp;#105;&amp;#46;&amp;#112;&amp;#115;&amp;#108;&amp;#46;&amp;#101;&amp;#117;

[1] H. Le, L. Vial, J. Frej, V. Segonne, M. Coavoux, B. Lecouteux, A. Allauzen, B. Crabbé, L. Besacier, Didier S. (2020) Flaubert: Unsupervised language model pre-training for French.  Proceedings of the 12th Language Resources and Evaluation Conference 
[2] Kemble, H., Eisenhauer, C., Couce, A., Chapron, A., Magnan, M., Gautier, G., Nghe, P. &amp;amp; Tenaillon, O. (2020). Flux, toxicity, and expression costs generate complex genetic interactions in a metabolic pathway. Science advances, 6(23), eabb2236.
[3] Nghe, P., Kogenaru, M., &amp;amp; Tans, S. J. (2018). Sign epistasis caused by hierarchy within signalling cascades. Nature communications, 9(1), 1-9.</description>
        <link>https://www.edpif.org/phorum/read.php?3,282,282#msg-282</link>
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            <guid>https://www.edpif.org/phorum/read.php?3,282,282#msg-282</guid>
            <title>Learning Genetic interactions with Deep neural Networks</title>
            <link>https://www.edpif.org/phorum/read.php?3,282,282#msg-282</link>
            <description><![CDATA[ The application of AI to biology is leading to revolutionary achievements with Alphafold for protein folding and generative models of artificial enzymes. However, a question remains open at a higher level of organization in cells, crucial for diagnosis and therapeutic strategies: how to predict the impact of multiple gene perturbations on biological functions? The aim of the project is to develop a deep learning approach leveraging on the one hand recent work on deep neural networks in the MILES team of Dauphine [1] and on the other hand experiments and mechanistic models developed at the ESPCI laboratory, showing that interactions between mutations are largely explained by non-linear but smooth functions of intermediate features [2-3]. How can we design a deep-learning model that can include these two steps of decomposition to learn gene interactions? <br />
<br />
For this purpose, the PhD will develop three complementary lines of research: (i) build deep nets on published datasets of combined genetic and drug perturbations on cells; (ii) computationally simulate the response of cells based on typical gene network architectures; (iii) apply the developed models to design, predict and interpret the outcome of large scale screening experiments done at ESPCI.<br />
<br />
The PhD will be co-supervised by Alexandre Allauzen, Professor at University Paris Dauphine and ESPCI  (team Machine Intelligence and LEarning Systems) and Philippe Nghe (director of the Laboratory of Biophysics and Evolution, ESPCI Paris-PSL). It is funded by the CNRS. Possible profiles include former experience in deep learning, computational biology, physics, mathematics. The position is expected  to start around September 2022.<br />
Contacts: <a href="mailto:&#97;&#108;&#101;&#120;&#97;&#110;&#100;&#114;&#101;&#46;&#97;&#108;&#108;&#97;&#117;&#122;&#101;&#110;&#64;&#100;&#97;&#117;&#112;&#104;&#105;&#110;&#101;&#46;&#112;&#115;&#108;&#46;&#101;&#117;">&#97;&#108;&#101;&#120;&#97;&#110;&#100;&#114;&#101;&#46;&#97;&#108;&#108;&#97;&#117;&#122;&#101;&#110;&#64;&#100;&#97;&#117;&#112;&#104;&#105;&#110;&#101;&#46;&#112;&#115;&#108;&#46;&#101;&#117;</a>;  <a href="mailto:&#112;&#104;&#105;&#108;&#105;&#112;&#112;&#101;&#46;&#110;&#103;&#104;&#101;&#64;&#101;&#115;&#112;&#99;&#105;&#46;&#112;&#115;&#108;&#46;&#101;&#117;">&#112;&#104;&#105;&#108;&#105;&#112;&#112;&#101;&#46;&#110;&#103;&#104;&#101;&#64;&#101;&#115;&#112;&#99;&#105;&#46;&#112;&#115;&#108;&#46;&#101;&#117;</a><br />
<br />
[1] H. Le, L. Vial, J. Frej, V. Segonne, M. Coavoux, B. Lecouteux, A. Allauzen, B. Crabbé, L. Besacier, Didier S. (2020) Flaubert: Unsupervised language model pre-training for French.  Proceedings of the 12th Language Resources and Evaluation Conference <br />
[2] Kemble, H., Eisenhauer, C., Couce, A., Chapron, A., Magnan, M., Gautier, G., Nghe, P. &amp; Tenaillon, O. (2020). Flux, toxicity, and expression costs generate complex genetic interactions in a metabolic pathway. Science advances, 6(23), eabb2236.<br />
[3] Nghe, P., Kogenaru, M., &amp; Tans, S. J. (2018). Sign epistasis caused by hierarchy within signalling cascades. Nature communications, 9(1), 1-9.]]></description>
            <dc:creator>pnghe</dc:creator>
            <category>Thèses hors de l&#039;EDPIF</category>
            <pubDate>Thu, 28 Apr 2022 20:10:19 +0200</pubDate>
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