Handles creating, reading and updating events.

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            "name": "Analyse statistique RNA-seq sous Galaxy",
            "shortName": "",
            "description": "\nObjectifs\n\nSe sensibiliser aux concepts et méthodes statistiques pour l'analyse de données transcriptomiques de type RNA-Seq.\nComprendre le matériel et méthodes (normalisation et tests statistiques) d'un article\ndu domaine.\nComprendre les particularités liées à la nature des données.\n\n \n \nProgramme\n\nPlanification expérimentale des expériences RNA-Seq (identification des biais, répétitions, biais contrôlables).\nNormalisation et analyse différentielle : recherche de \"régions d'intérêt\" différentiellement exprimées (modèle linéaire généralisé).\nPrise en compte de la multiplicité des tests.\nLe cours sera illustré par différents exemples et un jeu de données sera traité à l'aide du package R SARTools (basé sur les packages R DESeq2 et edgeR) dans les environnements Galaxy et RStudio.\n",
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            "name": "Perl avancé",
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            "description": "\nObjectifs\n\nAller plus loin avec Perl afin d’être autonome pour des manipulations complexes visant à extraire et reformater des données issues de fichiers texte.\n\n \n \n \n \nProgramme\n\n- Expressions régulières\n- Fonctions\n- Prise en main de Bioperl\n \n \nIllustration avec des exercices de manipulation de fichiers de séquences et de fichiers de résultats d’outils bionformatiques.\n \n",
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                "Programming Languages & Computer Sciences",
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            "name": "SHORT-READ ALIGNMENT AND SMALL SIZE VARIANTS CALLING - 13 avril 2026",
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            "description": "This training session, organized jointly with the Sigenae platform, is designed to introduce NGS data, in particular Illumina Solexa technologies with command line. You will discover the new sequence formats, the assembly formats and the known biases of these technologies. You will use mapping on reference genome software, polymorphisms detection with the GATK pipeline and alignment visualization software.\r\n\r\nThis training is focused on the practice. It consists of modules with a large variety of exercises:\r\n\r\nDay 1 (09:00 am to 12:30 am): Fastq format / Sequence quality. Read mapping.\r\nDay 1 (14:00 pm to 17:00 pm): SAM format. Visualisation.\r\nDay 2 (09:00 am to 17:00 am): Variant calling. VCF format. Variant annotation (SNPeff / SNPsift).\r\n \r\nThe session will take place in the room ‘salle de formation’ at INRAE center of Toulouse-Auzeville.\r\n\r\nPrerequisites: ability to use a Unix environment (see Unix training) and Cluster (see Cluster training).\r\n \r\nTool box: FastQC, BWA, Samtools, Picard tools, GATK, SnpSift / SnpEff, IGV.",
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                "Non-academic: 550€ + 20% taxes (TVA)",
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            "description": "Introduire Snakemake et vous permettre de présenter vos projets et retour d'expériences",
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            "city": "Bâtiment Lwoff – Salle retrovirus, Institut Pasteur, Paris",
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            "description": "Acquérir les compétences nécessaires à l’utilisation du logiciel R, connaître les principales analyses statistiques ...",
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            "updated_at": "2025-02-21T08:52:30.567397Z",
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            "name": "Formation \"Annotation & Analyse de Génomes Procaryotes - Mise en oeuvre de la Plateforme MicroScope\"",
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