<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Genomics on Hakim Bouazzaoui</title><link>https://hakim.bouazzaoui.fr/tags/genomics/</link><description>Recent content in Genomics on Hakim Bouazzaoui</description><generator>Hugo</generator><language>en-US</language><copyright>Copyright Hakim Bouazzaoui. Tous droits réservés sauf mention contraire.</copyright><lastBuildDate>Sun, 31 May 2026 00:00:00 +0000</lastBuildDate><atom:link href="https://hakim.bouazzaoui.fr/tags/genomics/index.xml" rel="self" type="application/rss+xml"/><item><title>Onkogene.com</title><link>https://hakim.bouazzaoui.fr/projects/onkogene/</link><pubDate>Sun, 31 May 2026 00:00:00 +0000</pubDate><guid>https://hakim.bouazzaoui.fr/projects/onkogene/</guid><description>&lt;p&gt;Onkogene.com is a scientific literature monitoring platform focused on genomic medicine of solid tumors. It surfaces curated articles of interest for oncologists, molecular geneticists and bioinformaticians working at the intersection of genomics and artificial intelligence.&lt;/p&gt;</description></item><item><title>MobiDeep</title><link>https://hakim.bouazzaoui.fr/projects/mobideep/</link><pubDate>Sun, 31 May 2026 00:00:00 +0000</pubDate><guid>https://hakim.bouazzaoui.fr/projects/mobideep/</guid><description>&lt;p&gt;MobiDeep is a project focused on prioritizing non-coding variants from whole-genome sequencing data. The underlying problem is central in rare diseases: non-coding regions represent a large part of the genome, remain difficult to interpret and may contribute to diagnostic delay.&lt;/p&gt;</description></item><item><title>The Clinical and Genetic Landscape of a French Multicenter Cohort of 2563 Epilepsy Patients</title><link>https://hakim.bouazzaoui.fr/publications/epigen-network-epilepsy-genetic-diagnosis/</link><pubDate>Fri, 01 Aug 2025 00:00:00 +0000</pubDate><guid>https://hakim.bouazzaoui.fr/publications/epigen-network-epilepsy-genetic-diagnosis/</guid><description>&lt;p&gt;Contribution to a French multicenter study on the clinical and genetic landscape of patients referred for genetic diagnosis of epilepsy.&lt;/p&gt;
&lt;h2 id="links"&gt;Links&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;DOI: &lt;a href="https://doi.org/10.1111/ene.70324"&gt;10.1111/ene.70324&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;PubMed: &lt;a href="https://pubmed.ncbi.nlm.nih.gov/40778729/"&gt;PMID 40778729&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;Europe PMC: &lt;a href="https://europepmc.org/article/MED/40778729"&gt;PMC12332890&lt;/a&gt;&lt;/li&gt;
&lt;/ul&gt;</description></item></channel></rss>