Handles creating, reading and updating training events.

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            "name": "Graphiques sous R avec ggplot2 / Graphics with R-ggplot2",
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            "name": "Initiation à l’utilisation de Galaxy",
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            "description": "Objectifs pédagogiques :\r\nCette formation propose une introduction sur l’interface utilisateur et les fonctionnalités générales d’une plateforme Galaxy.\r\nA l’issue de la formation, les apprenants seront en mesure de :\r\n* connaître les caractéristiques et le fonctionnement d’un portail Galaxy,\r\n* appliquer sur des cas concrets en bioinformatique,\r\n* être autonome dans le traitement de fichiers et l’exécution d’outils.\r\n\r\nProgramme :\r\n* Prise en main d’un portail Galaxy\r\n* Utilisation de l’historique\r\n* Téléchargement des données à traiter\r\n* Manipulation de fichiers\r\n* Paramétrage et exécution d’outils\r\n* Récupération et visualisation de résultats",
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            "id": 350,
            "name": "Formation Principes FAIR dans un projet de bioinformatique",
            "shortName": "FAIR-Bioinfo-Strasbourg",
            "description": "Cette formation sur 3 jours est destinée à des bioinformaticiens et biostatisticiens souhaitant acquérir des compétences théoriques et pratiques sur les principes \"FAIR\" (Facile à trouver, Accessible, Interopérable, Réutilisable) appliqués à un projet d'analyse et/ou de développement.",
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            "keywords": [
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                "Snakemake",
                "Docker"
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            ],
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            "accessConditions": "Academics",
            "maxParticipants": 14,
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                    "name": "IBMP",
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                },
                {
                    "id": 83,
                    "name": "IGBMC",
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            ],
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                    "id": 14,
                    "name": "BiGEst",
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            "updated_at": "2023-12-20T15:44:00.254606Z",
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            ],
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            "learningOutcomes": "A l'issue de cette formation, les participants pourront mettre en oeuvre les principes de la science reproductible : encapsuler un environnement de travail (Docker, Singularity), concevoir et exécuter des workflows (Snakemake), gérer des versions de code (Git), passer à l’échelle sur un cluster de calcul (Slurm), gérer des environnements logiciels (Conda) et assurer la traçabilité de leur analyse à l’aide de Notebooks (Jupyter).",
            "hoursPresentations": 10,
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            "personalised": false,
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            "id": 349,
            "name": "Reproducible Research",
            "shortName": "",
            "description": "The following topics and tools are covered in the course:\r\n\r\n    Data management\r\n    Project organisation\r\n    Git\r\n    Conda\r\n    Snakemake\r\n    Nextflow\r\n    R Markdown\r\n    Jupyter\r\n    Docker\r\n    Singularity\r\n\r\nAt the end of the course, students should be able to:\r\n\r\n    Use good practices for data analysis and management\r\n    Clearly organise their bioinformatic projects\r\n    Use the version control system Git to track and collaborate on code\r\n    Use the package and environment manager Conda\r\n    Use and develop workflows with Snakemake and Nextflow\r\n    Use R Markdown and Jupyter Notebooks to document and generate automated reports for their analyses\r\n    Use Docker and Singularity to distribute containerized computational environments",
            "homepage": "https://southgreenplatform.github.io/training_reproducible_research/",
            "is_draft": false,
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            ],
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                "Linux - Basic Knowledge"
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            "accessConditions": "Open to South Green close collaborators",
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            "logo_url": "https://southgreenplatform.github.io/trainings//images/southgreenlong.png",
            "updated_at": "2023-12-04T15:16:00.921744Z",
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            "difficultyLevel": "Novice",
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            "learningOutcomes": "At the end of the course, students should be able to:\r\n\r\n    Use good practices for data analysis and management\r\n    Clearly organise their bioinformatic projects\r\n    Use the version control system Git to track and collaborate on code\r\n    Use the package and environment manager Conda\r\n    Use and develop workflows with Snakemake and Nextflow\r\n    Use R Markdown and Jupyter Notebooks to document and generate automated reports for their analyses\r\n    Use Docker and Singularity to distribute containerized computational environments",
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            "personalised": null,
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                "https://catalogue.france-bioinformatique.fr/api/event/567/?format=api"
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        },
        {
            "id": 294,
            "name": "Linux for Dummies",
            "shortName": "",
            "description": "This course offers an introduction to work with Linux. We will describe the Linux environment, the first linux commands so participants can start to utilize command-line tools and feel comfortable using bioinformatics softwares through a linux terminal",
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            ],
            "logo_url": "https://southgreenplatform.github.io/trainings//images/southgreenlong.png",
            "updated_at": "2023-12-04T15:05:31.847400Z",
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                "https://catalogue.france-bioinformatique.fr/api/event/468/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/555/?format=api"
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        },
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            "id": 313,
            "name": "RNA-Seq analysis",
            "shortName": "",
            "description": "Introduction to RNA-Seq analysis",
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            "is_draft": false,
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            "prerequisites": [
                "Linux - Basic Knowledge"
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            "openTo": "Internal personnel",
            "accessConditions": "Open to South Green close collaborators",
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            "logo_url": "https://southgreenplatform.github.io/trainings//images/southgreenlong.png",
            "updated_at": "2023-12-04T15:04:39.023455Z",
            "audienceTypes": [],
            "audienceRoles": [],
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            "trainingMaterials": [],
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            "hoursTotal": 14,
            "personalised": false,
            "event_set": [
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                "https://catalogue.france-bioinformatique.fr/api/event/471/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/563/?format=api"
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        {
            "id": 347,
            "name": "Introduction to Microbial Comparative Genomics",
            "shortName": "",
            "description": "This course offers an introduction to microbial genomics analysis.\r\nIt includes 5 issues: assembly, genome annotation, circos visualization, pan-genome construction, pan-GWAS.",
            "homepage": "https://southgreenplatform.github.io/trainings//bacterialGenomics/",
            "is_draft": false,
            "costs": [
                "Free"
            ],
            "topics": [],
            "keywords": [
                "genomics",
                "Structural genomics",
                "Genome analysis"
            ],
            "prerequisites": [
                "Linux - Basic Knowledge"
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            "accessConditions": "Open to South Green close collaborators",
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                "https://catalogue.france-bioinformatique.fr/api/userprofile/771/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/userprofile/772/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/userprofile/773/?format=api"
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            "logo_url": "https://southgreenplatform.github.io/trainings//images/southgreenlong.png",
            "updated_at": "2023-12-04T14:54:55.468140Z",
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            "id": 348,
            "name": "Advanced HPC Trainings",
            "shortName": "",
            "description": "This course continues the explanation on how to work on HPC Southgreen clusters. It is intended for experienced users, with the goals of improving LC user productivity and minimizing the obstacles. New notions and tools are presented such as job arrays, basic softwares installation,module environment and singularity. All these notions will be developped.",
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            "is_draft": false,
            "costs": [
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            "topics": [],
            "keywords": [
                "HPC",
                "SLURM"
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            "accessConditions": "Oprn to South Green close collaborators",
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                "R programming"
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            "openTo": "Everyone",
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            "prerequisites": [
                "Linux - Basic Knowledge"
            ],
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            "updated_at": "2023-06-14T10:18:52.160465Z",
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        {
            "id": 334,
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            "description": "Researchers often have access to or generate multiple omics data (RNAseq, metabolomics, lipidomics, proteomics…) within a single study. Although each omics data is usually analyzed individually, combining complementary data can yield a better understanding of the mechanisms involved in biological processes. Several integrative approaches are now available to combine such data, coming essentially from two families of methods, namely multivariate statistical analyses and network-based approaches. During this summer school both methodologies will be covered, introducing RGCCA and mixOmics for multivariate analyses and WGCNA and SNF for network-based strategies. To get meaningful biological information, the interpretation of statistical results needs to be done contextualizing them in the available biological knowledge. To address this major step we need to be able to access and interrogate databases. We will harness this subject introducing semantic web and knowledge graphs in the context of metabolic networks.\r\n\r\nDuring the School, significant time will be devoted to hands-on and the program will be divided into three phases / topics:\r\n- Multivariate statistical analyses (Instructors: Arnaud Gloaguen & Jimmy Vandel)\r\n- Network-based approaches (Instructors: Morgane Térézol & Marie-Galadriel Brière)\r\n- Results contextualisation: an introduction to metabolic models, web semantic and knowledge graphs (Instructors: Jean-Clément Gallardo, Maxime Delmas & Marco Pagni)\r\n\r\nThe participants will work in groups and shortly present the application of what they have learned to their own project.",
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                "Multivariate analyses",
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            ],
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            "updated_at": "2023-04-26T16:14:06.237852Z",
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        },
        {
            "id": 272,
            "name": "Molecular Phylogeny - Level 2",
            "shortName": "Phylogénie moléculaire - Niveau 2",
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            "homepage": "",
            "is_draft": false,
            "costs": [
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                "1200 €"
            ],
            "topics": [],
            "keywords": [
                "Phylogeny",
                "Selection Detection",
                "Phylogenomics"
            ],
            "prerequisites": [],
            "openTo": "Everyone",
            "accessConditions": "",
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            ],
            "logo_url": "https://ressources.france-bioinformatique.fr/sites/default/files/ATGClogox120_0.png",
            "updated_at": "2023-01-24T10:49:17.913427Z",
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            "event_set": [
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        },
        {
            "id": 271,
            "name": "Bioinformatique pour le traitement de données de séquençage (NGS) : analyse de transcriptome",
            "shortName": "",
            "description": "OBJECTIFS\r\n- Comprendre les principes des méthodes d'analyse de données de séquençage à haut débit\r\n- Comprendre les résultats obtenus, les paramètres et leurs impacts sur les analyses\r\n- Savoir choisir et utiliser les principaux outils d'analyse\r\n- Être autonome pour utiliser un pipeline d'analyse\r\n- Savoir manipuler les fichiers de séquences : préparation et filtration\r\n- Savoir évaluer la qualité des données\r\n- Savoir analyser les résultats avec ou sans génome de référence\r\n\r\nPRÉREQUIS\r\n- Notions de base en informatique : fichiers, répertoire...\r\n- Notions du système linux et des lignes de commande\r\n- Niveau master \r\n\r\nPROGRAMME\r\n- Linux : commandes de base\r\n- Les données NGS : fichiers, manipulation de base, nettoyage\r\n- Mapping : principaux outils et pratique\r\n- Transcriptomique :\r\n. analyse de RNA-seq : expression différentielle des gènes / des ARNs (comptage et DESeq2) ; comparaison d'échantillons issus de conditions différentes\r\n. post-analyse : analyse GO, interrogation bases de connaissances (ex : KEGG), création de graphique (en R)\r\n. analyse couplée transcriptome / traductome",
            "homepage": "",
            "is_draft": false,
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            ],
            "topics": [],
            "keywords": [
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            "prerequisites": [],
            "openTo": "Everyone",
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                    "name": "ATGC",
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            ],
            "logo_url": "https://ressources.france-bioinformatique.fr/sites/default/files/ATGClogox120.png",
            "updated_at": "2023-01-24T10:47:30.457628Z",
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            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/401/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/510/?format=api"
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        },
        {
            "id": 306,
            "name": "Molecular Phylogeny - Level 1",
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            "homepage": "",
            "is_draft": false,
            "costs": [
                "1200 €"
            ],
            "topics": [
                "http://edamontology.org/topic_0084",
                "http://edamontology.org/topic_3293",
                "http://edamontology.org/topic_3299"
            ],
            "keywords": [],
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            "updated_at": "2023-01-24T10:44:55.936489Z",
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            "audienceRoles": [],
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            "learningOutcomes": "To know how to infer a phylogenetic tree and interpret it.",
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            "description": "Program\r\n\r\n*  Handling mapping tools suitable for ILLUMINA and ONT data (bwa, minimap2)\r\n*  SNP detection from mapping of short reads against a reference genome: SNP calling, filters and SNP annotation. Examples of possible studies based on SNP arrays\r\n* Detecting Structural Variations (SV) in short and long reads (breakdancer, sniffle)\r\n* SV detection from genome assembly and comparison (minimap2, nucmer, assemblytics, siry)",
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            "name": "RNASeq analyses (using Galaxy and TOGGLe)",
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            "description": "This course offers an introduction to RNASeq analyses using two different workflow management systems: Galaxy and TOGGLe. This includes reference-based mapping, estimates of transcript levels, differential expression (DE) analyses, visualization of statistics results.\r\nPrerequisites\r\nWorkflow management system (Galaxy, TOGGLe)\r\n\r\nProgram\r\nMapping of RNASeq against a transcriptome reference with kallisto (Galaxy)\r\nMapping of RNASeq against an annotated genome reference with TopHat (TOGGLe)\r\nDifferential expression analysis using EdgeR and DESeq2\r\nPlots, clustering, co-expression network: degust, WGCNA\r\n\r\n\r\nLearning objectives\r\nManipulate packages/tools available for searching DE genes\r\nThink about different normalisation methods\r\nDetect differentially expressed genes\r\nCompare results between two approaches\r\n\r\n\r\nInstructors\r\nAlexis Dereeper - alexis.dereeper@ird.fr\r\nSebastien Cunnac - sebastien.cunnac@ird.fr\r\nSebastien Ravel - sebastien.ravel@cirad.fr\r\nChristine Tranchant  - christine.tranchant@ird.fr",
            "homepage": "https://southgreenplatform.github.io/trainings//rnaseq/",
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            "description": "This course offers an introduction to metabarcoding analyses at two different levels/steps: bioinformatics with FROGS pipeline in the Galaxy environment, biostatistics with PhyloSeq R package. This includes preprocessing, clustering and OTU picking, taxonomic assignation, estimation of diversity, visualization of statistics results.\r\nPrerequisites\r\nGalaxy, R knowledge\r\n\r\nProgram\r\nIntroduction to metagenomics and metabarcoding\r\nPre-processing, Clustering, taxonomic affiliation (FROGS)\r\nHandling and visualizing OTU table using PhyloSeq R package (PhyloSeq)\r\n\r\n\r\nLearning objectives\r\nManipulate tools available for metabarcoding analysis\r\nStudy sample diversity by using NGS and post-NGS analysis tools\r\nVisualize diversity metrics in metabarcoding approach​\r\n\r\n\r\nInstructors\r\nJulie Orjuela - julie.orjuela@ird.fr\r\nFlorentin Constancias - florentin.constancias@cirad.fr\r\nAlexis Dereeper - alexis.dereeper@ird.fr",
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