Handles creating, reading and updating training events.

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            "name": "Biotechnologies et bioinformatique appliquées aux maladies rares",
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            "description": "Module optionnel du DIU Maladies rares : de la recherche au traitement.\n",
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                "Autre (Diplôme universitaire, école d'ingénieur ...)"
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            "id": 147,
            "name": "Linux et script pour la bioinformatique",
            "shortName": "",
            "description": "Pour la plupart des tâches communes, le système Linux (libre et gratuit) peut avantageusement remplacer les systèmes d'exploitation propriétaires tels que Windows ou MacOS. Les énormes avantages de Linux sont sa gratuité, son évolution constante et l'inexistence des virus. Ce stage est une initiation à l'utilisation du système d'exploitation Linux et des lignes de commande pour les non informaticiens, ainsi qu'une initiation à l'écriture et l'emploi de scripts (petits programmes) pour faciliter l'analyse de données. Il s'agit pour des débutants ou quasi débutants Linux d'utiliser le système et d'acquérir l'autonomie nécessaire pour résoudre les besoins communs simples d'analyse par la combinaison des méthodes à travers des scripts.\n \n",
            "homepage": "http://cnrsformation.cnrs.fr/stage-17285-Linux-et-script-pour-la-bioinformatique…",
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            "id": 80,
            "name": "Bioinformatique pour le traitement de données de séquençage (NGS)",
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            "description": "\nLes objectifs sont :\n- Savoir choisir les outils d'analyse\n- Etre autonome pour effectuer un pipeline d'analyse\n- Comprendre les principes des méthodes d'analyse\n- Savoir manipuler les fichiers de séquences : préparation et filtration\n- Etre capable d'évaluer la qualité des données\n- Savoir analyser avec ou sans génome de référence\nhttps://cnrsformation.cnrs.fr/\n\n",
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            "name": "Phylogénie moléculaire",
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            "description": "\nLes objectifs sont :\n1. Acquérir des connaissances théoriques et pratiques en phylogénie moléculaire.\n2. Être autonome dans la conduite d'une analyse phylogénétique.\n3. Maîtriser le choix, le paramétrage et l'exploitation des résultats des programmes de phylogénie.\nhttps://cnrsformation.cnrs.fr/\n\n",
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            "description": "The aim of this course is to provide students with theory and practical\ntools to analyze Next Generation Sequencing (NGS) data.  The course is\ncomposed of a theory and practice lessons . In the first week theory\nsessions will cover the main kind of HTS analyses (re-sequencing and\nvariant analysis, de-novo sequencing, transcriptomics, ChIP-Seq,\nmetagenomics), in addition to some general bioinformatics tools and\nBiostatistics. The second week is dedicated to practice, in which the\nstudents work with their own data in small groups with a mentor that\nguides them. The practice week is designed so the course is of immediate\nuse to each student. We expect the students to go back to their countries\nwith the necessary knowledge to continue working on their own data.\n",
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            "name": "Introduction à la phylogénie moléculaire",
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            "description": "Le C3BI propose des cours pour acquérir les notions théoriques de phylogénie et maitriser les outils et logiciels.\nLes cours d'”Introduction à la phylogénie moléculaire” sont ouverts EN ACCES LIBRE  à tous les Pasteuriens et dispensés en langue française .\nl'après midi les travaux pratiques sont limités à 15 personnes (sur inscription)\n** Mardi 29 septembre\n– 9h30-11h : Méthodes de distance (A. Criscuolo)\n– 14h-15h30 : Méthodes de Maximum de Parcimonie (O. Gascuel)\n** Mercredi 30 septembre\n– 9h30-11h : Modèles d’évolution (O. Gascuel)\n– 14h-15h30 : Méthodes de Maximum de Vraisemblance (O. Gascuel)\n** Jeudi 1er octobre\n– 9h30-11h : Méthodes Bayesiennes (G. Perriere)\n– 14h-15h30 : Inférences des forces sélectives (G. Perriere)\n",
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            "description": "As the command line training but with Galaxy. Organized jointly by the Sigenae and Bioinfo Genotoul platforms.\n",
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            "description": "This training session is designed to help you to deal with small RNA sequences produced from the SGS (Second Generation Sequencing) technology particularly Illumina platforms (HiSeq). You will discover sequence file formats, learn about expression profiles of miRNA and other small non coding RNA and run different kind of analysis such as reads cleaning, alignment on a reference genome, detection and annotation of new and known miRNA, and expression quantification. Organized jointly by the Sigenae and bioinfo genotoul platforms.\n",
            "homepage": "http://bioinfo.genotoul.fr/index.php/events/srnaseq/",
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            "name": "Sequences alignment and phylogeny ",
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            "description": "This training session is organized by the bios4Biol CATI and the genotoul bioinfo platform and aims at initiating participants to molecular phylogenetics studies.\nYou will discover how to build a sequence dataset, to align sequences, to edit and refine the resulting alignment.\n",
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            "description": "This training session has been designed to give you an overview of the methods and tools used to de novo assemble transcriptomic short reads. You will learn how to pre-process your raw data (fastq files), how an assembler works and how to use it. Finally you will learn how to assess the quality of your assemblies in order to choose the best one. Organized jointly by the Sigenae and bioinfo genotoul platforms.\n",
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            "id": 70,
            "name": "Phylogenomy and selection pressure ",
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            "description": "This training session is organized by the bios4Biol CATI.\nMorning : phylogenomics\nThe morning course will provide insigths about sampling problems in phylogenomics studies (genes, species) and methodological aspects of phylogenomics studies with two major focus on super-matrix and super-tree methods.\nAfternoon : selection pressure\nThe afternoon course will be dedicated to the use of the PAML4 package in order to study selection pressures in a sequence alignment.\n",
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            "name": "Using sed and awk to modify large large text files",
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            "description": "Many analysis generate large result text files which have to be checked, merged, split, reduced. Several tools have been developed and are available on Unix to do this, including sed and AWK. During this course you will be trained to process large files with sed and AWK. Sed is tool enabling to select and process lines. You can easily insert, delete, modify, append lines to very large files with millions of lines. AWK will enable to perform more fine tuned file modifications based on columns. It includes also more mathematical and string functions.  The course is based mainly on exercises with small sections presenting concepts and commands.",
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                "Academic but non-INRAE: 170 € + 20% taxes (TVA)",
                "For INRAE's staff: 150 € no VAT charged;"
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                "https://catalogue.france-bioinformatique.fr/api/event/479/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/611/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/631/?format=api",
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            "id": 69,
            "name": "Methods for phylogenetics trees construction",
            "shortName": "",
            "description": "This training session is organized by the bios4Biol CATI and aims at training participants to construct and interpret phylogenetic trees.\nYou will discover how to choose an evolutionary model and a phylogenetic inference method (among distance, parsimony, maximum likelihood and Bayesian methods) and how to evaluate the robustness of a tree using bootstrap.\n",
            "homepage": "http://bioinfo.genotoul.fr/index.php/events/methods-for-phylogenetic-trees-const…",
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            "keywords": [
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                "Evolution and Phylogeny",
                "Molecular evolution",
                "Genes and genomes"
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            "openTo": "Internal personnel",
            "accessConditions": "You need to register (via the website) and pay 165 euros a day for academic and 550 euros a day for a private.\n",
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            "id": 144,
            "name": "FROGS formation : tools for bioinformatics and statistics analyses with amplicon metagenomics data",
            "shortName": "",
            "description": "This training session, organized by Bioinfo Genotoul, Sigenae, NED (GenPhySE) and TWB, is designed to help you to deal with NGS data of 16S, 18S ... DNA produced with MiSeq from Illumina and Roche 454 technologies in the Galaxy workbench.\nYou will discover how to use our Galaxy instance, clean reads, clusterize them, do the taxonomic affiliation and perform statistics to interpret your results.\nPrerequisites: knowledge of R or in another programming language\n",
            "homepage": "http://bioinfo.genotoul.fr/index.php/events/metagenomic-amplicons-and-stats-with…",
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            ],
            "topics": [],
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            "prerequisites": [],
            "openTo": "Internal personnel",
            "accessConditions": "Subscribe by the web page : http://bioinfo.genotoul.fr/index.php/training-2/galaxy-training/.\nPrices : 165 euros per day for academic people, 550 per day otherwise.\n",
            "maxParticipants": null,
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        },
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            "name": "LINUX",
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            "description": "This training session is organized by the Genotoul bioinfo platform and aims at learning sequence analysis. This training session has been designed to familiarize yourself with the platform resources and its organization. You will learn to access the platform from your work station, what is an Linux environment and how to use it, how to create and manipulate files, how to transfer them from and to your personal computer.\r\n\r\nThis training is focused on practice. It consists of 3 modules with a large variety of exercises:\r\n\r\n- Connect to « genotoul » server (09:00 am to 10:30 am): Platform presentation, Linux basics, opening an user account, Putty installation, first connection.\r\n- Files and basics commands  (10:45 am to 12:00 pm): types of files and secure access, file manipulation commands, text editors and viewers, disk space management .\r\n- Transfers and file manipulation (14:00 pm to 17:00 pm): download/transfer, compress/uncompress, utility commands and data extraction, output redirections.",
            "homepage": "http://bioinfo.genotoul.fr/index.php/events/linux-2-2/",
            "is_draft": false,
            "costs": [
                "Non-academic: 550€ + 20% taxes (TVA)",
                "Academic but non-INRAE: 170 € + 20% taxes (TVA)",
                "For INRAE's staff: 150 € no VAT charged;"
            ],
            "topics": [
                "http://edamontology.org/topic_3316"
            ],
            "keywords": [],
            "prerequisites": [
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            ],
            "openTo": "Everyone",
            "accessConditions": "",
            "maxParticipants": 10,
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            ],
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            ],
            "logo_url": "http://bioinfo.genotoul.fr/wp-content/uploads/bioinfo_logo-rvb-petit.png",
            "updated_at": "2024-06-05T08:59:07.762580Z",
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            ],
            "audienceRoles": [
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            ],
            "difficultyLevel": "Novice",
            "trainingMaterials": [],
            "learningOutcomes": "You will learn to access the platform genotoul bioinfo from your work station, what is an Linux environment and how to use it, how to create and manipulate files, how to transfer them from and to your personal computer.",
            "hoursPresentations": 3,
            "hoursHandsOn": 3,
            "hoursTotal": 6,
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        },
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            "id": 71,
            "name": "Galaxy : first step",
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            "description": "Galaxy is a workbench available for biologists from Sigenae Platform. Galaxy objectives are:\n    First, making bioinfo Linux tools accessible to biologists.\n    Then, it is possible to add Linux tools by developpers into Galaxy workbench.\n    Then, Galaxy is used to hide the complexity of the infrastructure and to allow creation, execution and sharing of workflows.\nYou will acquire the following competencies required for the other Galaxy trainning:\n    Login to Galaxy: Galaxy Workbench (To access to Galaxy, you need to have an LDAP Genotoul login and password).\n    Begin to use some tools provided (BWA, SAM tools, FastQC).\n    Work on files.\nOrganized jointly by the Sigenae and the Bioinfo Genotoul platform.\n",
            "homepage": "http://bioinfo.genotoul.fr/index.php/events/first-step-with-galaxy/",
            "is_draft": false,
            "costs": [
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            ],
            "topics": [],
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                "NGS Sequencing Data Analysis"
            ],
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            "openTo": "Internal personnel",
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            "name": "Cluster",
            "shortName": "",
            "description": "This training session is designed to help you deal with the platform compute cluster and data banks. You will launch your first processing batch on the cluster and will learn how to track and manage them. Organized jointly by the Sigenae and bioinfo genotoul platforms.",
            "homepage": "http://bioinfo.genotoul.fr/index.php/events/cluster-2/",
            "is_draft": false,
            "costs": [
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                "For INRAE's staff: 150 € no VAT charged;"
            ],
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            "keywords": [
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                "Cluster"
            ],
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            ],
            "openTo": "Everyone",
            "accessConditions": "You need to register (via the website) and pay 170 euros a day for academic and 550 euros a day for a private.",
            "maxParticipants": 12,
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            ],
            "logo_url": "https://ressources.france-bioinformatique.fr/sites/default/files/bioinfo_logo-RVB_4.jpg",
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                {
                    "id": 140,
                    "name": "TP Cluster",
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                }
            ],
            "learningOutcomes": "",
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                "https://catalogue.france-bioinformatique.fr/api/event/477/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/610/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/261/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/633/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/668/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/529/?format=api"
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        },
        {
            "id": 64,
            "name": "Read alignment and SNP calling",
            "shortName": "",
            "description": "This training session, organized jointly with the Sigenae platform, is designed to help you deal with NGS data, in particular Roche 454 and Illumina Solexa technologies. You will discover the new sequence formats, the new assembly formats and the known biases of these technologies. You will use mapping on reference genome software, polymorphisms detection (with the GATK pipeline), polymorphisms annotation and alignment visualization software. Organized jointly by the Sigenae and bioinfo genotoul platforms.\n",
            "homepage": "http://bioinfo.genotoul.fr/index.php/events/alignment-and-small-size-variants-ca…",
            "is_draft": false,
            "costs": [
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            ],
            "topics": [],
            "keywords": [
                "NGS Data Analysis",
                "Variant analysis",
                "Genomics (DNA-seq)"
            ],
            "prerequisites": [],
            "openTo": "Internal personnel",
            "accessConditions": "You need to register (via the website) and pay 165 euros a day for academic and 550 euros a day for a private.\n",
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