Handles creating, reading and updating training events.

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            "learningOutcomes": "- Acquérir les compétences nécessaires à l’utilisation du logiciel R\r\n- Connaître les principales analyses statistiques nécessaires en biologie et les utiliser sous R\r\n- Réaliser des graphiques sous R\r\n- Connaitre les bibliothèques R utiles en Biologie",
            "hoursPresentations": 9,
            "hoursHandsOn": 12,
            "hoursTotal": 21,
            "personalised": false,
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        },
        {
            "id": 289,
            "name": "Introduction to galaxy: looking for variants in prokaryotes",
            "shortName": "Introduction to galaxy",
            "description": "This course will focus on the technical aspects of using a galaxy server. Accessible without any prerequisite in computer science, it will allow you to master the different fundamental tools of galaxy and will open the doors of bioinformatics analysis for your different projects.\r\nDifferent questions will be addressed through an example of variants analysis in a prokaryotic organism. At the end of this course, on any accessible galaxy instance, you will be able to:\r\n- upload your data\r\n- map them on a reference genome\r\n- find the variants (SNPs) and analyze the results\r\n- generate, manipulate and share your workflows, data and histories\r\n- find the right tools for other analyses and use them in your own project.\r\n\r\nUnless all participants speak French, the course will be taught in English.",
            "homepage": "https://pliniuscursus.univ-amu.fr/formation/galaxy-platform/",
            "is_draft": false,
            "costs": [
                "Free to academics"
            ],
            "topics": [
                "http://edamontology.org/topic_0091",
                "http://edamontology.org/topic_0622"
            ],
            "keywords": [],
            "prerequisites": [
                "Master"
            ],
            "openTo": "Internal personnel",
            "accessConditions": "The first sessions are only available for IM2B students.",
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                    "id": 23,
                    "name": "PACA-Bioinfo",
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                }
            ],
            "logo_url": null,
            "updated_at": "2022-06-02T11:50:50.812642Z",
            "audienceTypes": [
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            ],
            "audienceRoles": [
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            ],
            "difficultyLevel": "Novice",
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            "hoursPresentations": 1,
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            "id": 377,
            "name": "RNASEQ ALIGNMENT, QUANTIFICATION AND TRANSCRIPT DISCOVERY WITH STATISTICS",
            "shortName": "RNASeq bioinfo / biostat",
            "description": "The Toulouse Genotoul bioinformatics platform, in collaboration with the Genotoul Biostatistics platform, and the MIAT unit, organize a 3,5 days long training course for bio-informaticians and biologists aiming at learning sequence analysis. It focuses on (protein coding) gene expression analysis using reads produced by ‘RNA-Seq’. This training session is designed to introduce sequences from ‘NGS’ (Next Generation Sequencing), particularly Illumina platforms (HiSeq). You will discover the standards file formats, learn about the usual biases of this type of data and run different kinds of analyses, such as spliced alignment on a reference genome, novel gene and transcript discovery, expression quantification of coding genes and transcripts. Finally you will be able to extract the differentially expressed genes.",
            "homepage": "https://bioinfo.genotoul.fr/index.php/events/rnaseq-alignment-transcripts-assemblies-statistics/",
            "is_draft": false,
            "costs": [
                "Non-academic: 550€ + 20% taxes (TVA)",
                "Academic but non-INRAE: 170 € + 20% taxes (TVA)",
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            ],
            "topics": [
                "http://edamontology.org/topic_3308",
                "http://edamontology.org/topic_0203"
            ],
            "keywords": [
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                "Langage R de base",
                "Linux/Unix",
                "Cluster"
            ],
            "openTo": "Everyone",
            "accessConditions": "Register on the training page : https://bioinfo.genotoul.fr/index.php/training-2/training/",
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            "updated_at": "2025-12-01T11:55:30.468881Z",
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                "Life scientists",
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            "difficultyLevel": "Intermediate",
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                },
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                    "name": "training RNASeq biostat part",
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            ]
        },
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            "id": 324,
            "name": "Python scripts for bioinformatics and Linux",
            "shortName": "Scripts en Python pour la bioinformatique et environnement Linux",
            "description": "OBJECTIFS\r\n- Connaître les principes et les avantages du système Linux\r\n- Connaître et savoir utiliser les commandes de base permettant de lancer des programmes sous Linux\r\n- Comprendre et savoir lancer des scripts\r\n- Être capable d'écrire des scripts en Python\r\n- Acquérir de l'autonomie pour effectuer des analyses bioinformatiques qui combinent plusieurs outils \r\n\r\nPRÉREQUIS\r\n- Notions de base en informatique : fichiers, répertoires, etc. \r\n\r\nPROGRAMME\r\n- Linux : lignes de commandes, principales commandes, redirection\r\n- Lancer, créer et modifier des scripts\r\n- Notions de variables, de boucles, de choix\r\n- Programmation de scripts : utilisation de paramètres et de variables, combinaison d'outils et de logiciels, écriture des résultats dans un ou plusieurs fichiers\r\n- Création d'un pipeline d'outils",
            "homepage": "",
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            "costs": [
                "1200 €"
            ],
            "topics": [],
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                "Linux",
                "Python Language"
            ],
            "prerequisites": [],
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            "accessConditions": "",
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            ],
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                    "id": 7,
                    "name": "ATGC",
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            ],
            "logo_url": "https://www.france-bioinformatique.fr/sites/default/files/ATGClogox120_0.png",
            "updated_at": "2025-01-23T13:50:29.570608Z",
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            "event_set": [
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                "https://catalogue.france-bioinformatique.fr/api/event/703/?format=api"
            ]
        },
        {
            "id": 279,
            "name": "Annotation and analysis of prokaryotic genomes using the MicroScope platform",
            "shortName": "MicroScope training",
            "description": "In an effort to inform members of the research community about our annotation methods, to provide training for collaborators and other scientists who use the MicroScope platfom, and to inform scientific public on the analysis available in PkGDB (Prokaryotic Genome DataBase), we have developed a 4.5-day course in Microbial Genome Annotation and Comparative Analysis using the MaGe graphical interfaces.\r\n\r\nThis course will familiarize attendees with LABGeM’s annotation pipeline and the manual annotation software MaGe (Magnifying Genome) . No specific bioinformatics skill is required: detailed instruction on the algorithm developed in each annotation methods can be found in specific training courses on «Genomic sequences analysis». Here we focus on the general idea behind each method and, above all, the way you can interpret the corresponding results and combine them with other evidences in order to change or correct the current automatic functional annotation of a given gene, if necessary.\r\n\r\nThis course will also describe how to perform effective searches and analysis of procaryotic data using the graphical functionalities of the MaGe’s interfaces. Because of the numerous pre-computation available in our system (results of “common” annotation tools, synteny with all complete bacterial genomes, metabolic pathway reconstruction, fusion/fission events, genomic islands, …), many practical exercises allow attendees to get familiar with the use the MaGe graphical interfaces in order to efficiently explore these sets of results.",
            "homepage": "https://labgem.genoscope.cns.fr/professional-trainings/microscope-professional-trainings/training-annotation-analysis-of-prokaryotic-genomes-using-the-microscope-platform/",
            "is_draft": false,
            "costs": [
                "Priced"
            ],
            "topics": [
                "http://edamontology.org/topic_0797",
                "http://edamontology.org/topic_0085",
                "http://edamontology.org/topic_3301"
            ],
            "keywords": [],
            "prerequisites": [
                "Licence"
            ],
            "openTo": "Everyone",
            "accessConditions": "External training sessions can also be scheduled on demand, in France or abroad. See : https://labgem.genoscope.cns.fr/professional-trainings/microscope-professional-trainings/external-microscope-professional-training-sessions/",
            "maxParticipants": 12,
            "contacts": [],
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                {
                    "id": 15,
                    "name": "Laboratory of Bioinformatics Analyses for Genomics and Metabolism",
                    "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/Laboratory%20of%20Bioinformatics%20Analyses%20for%20Genomics%20and%20Metabolism/?format=api"
                }
            ],
            "organisedByOrganisations": [
                {
                    "id": 67,
                    "name": "University Paris-Saclay",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/University%20Paris-Saclay/?format=api"
                }
            ],
            "organisedByTeams": [
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                    "id": 9,
                    "name": "MicroScope",
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            ],
            "logo_url": "https://ressources.france-bioinformatique.fr/sites/default/files/plateforme-logo/MicroScope_logo.png",
            "updated_at": "2022-06-02T11:50:50.812642Z",
            "audienceTypes": [
                "Undergraduate",
                "Graduate",
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            "audienceRoles": [
                "Researchers",
                "Life scientists",
                "Biologists",
                "Curators"
            ],
            "difficultyLevel": "Intermediate",
            "trainingMaterials": [],
            "learningOutcomes": "Annotation and comparative analysis of bacterial genomes:\r\n\r\n- acquire theoretical and practical knowledge of genome annotation tools (structural and functional annotation, metabolic networks annotation)\r\n- interpret the results of functional annotation tools\r\nperform various comparative analyses : conserved synteny analyses, pan-genome, phylogenetic and metabolic profiles.\r\n- analyse the results of metabolic networks prediction tools and look for candidate genes for enzyme activities.\r\n- use the tools to analyse the genome(s) of interest of participants",
            "hoursPresentations": null,
            "hoursHandsOn": null,
            "hoursTotal": 31,
            "personalised": false,
            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/439/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/506/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/436/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/507/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/577/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/576/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/659/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/658/?format=api"
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        },
        {
            "id": 333,
            "name": "Improve your command line skills by learning a few words of Perl",
            "shortName": "",
            "description": "This “Perl one-liners” training session is organized by the Sigenae platform. Perl one-liners are small and awesome Perl programs that fit in a single line of code and perform many operations such as replacing of text, spacing, deleting, calculation, manipulation in files and many more. This training will allow you to discover the power of Perl on the command line and learn how to use it to automate your file manipulations and command line generation with classical file formats such as tabulated text, fastq, sam/bam, and vcf.\r\n\r\nThis training lasts one day and is focused on practice. It consists of 3 parts with a large variety of exercises:\r\n\r\nIntroduction to Perl and its characteristics: Perl is a widely used programming language for data processing and task automation. We will introduce the main characteristics of Perl and discuss why it is particularly suited for biologists who want to manipulate files and generate command lines.\r\nPerl on the command line: we will show how to use Perl on the command line to perform common tasks, such as searching and replacing strings, merging files, and loop over lists of files.\r\nConcrete examples: we will present several concrete examples drawn from biology, such as extracting information from genomic sequence files, converting files between different formats, and generating command lines for data biology tools.\r\n \r\nThe session will take place in the room ‘salle de formation MIAT’ at INRAE center of Toulouse-Auzeville.",
            "homepage": "https://bioinfo.genotoul.fr/index.php/events/onelineperl/",
            "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": [],
            "keywords": [
                "Perl Langage"
            ],
            "prerequisites": [
                "Linux/Unix",
                "Cluster"
            ],
            "openTo": "Everyone",
            "accessConditions": "",
            "maxParticipants": 12,
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                {
                    "id": 37,
                    "name": "MIAT - Mathématiques et Informatique Appliquées de Toulouse",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/MIAT%20-%20Math%C3%A9matiques%20et%20Informatique%20Appliqu%C3%A9es%20de%20Toulouse/?format=api"
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            ],
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                    "id": 22,
                    "name": "Genotoul-bioinfo",
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                }
            ],
            "logo_url": null,
            "updated_at": "2025-12-01T11:56:55.465635Z",
            "audienceTypes": [],
            "audienceRoles": [],
            "difficultyLevel": "Novice",
            "trainingMaterials": [
                {
                    "id": 148,
                    "name": "One line perl",
                    "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/One%20line%20perl/?format=api"
                }
            ],
            "learningOutcomes": "",
            "hoursPresentations": 3,
            "hoursHandsOn": 3,
            "hoursTotal": null,
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            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/531/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/723/?format=api"
            ]
        },
        {
            "id": 381,
            "name": "HOW TO RUN A NF-CORE NEXTFLOW WORKFLOW ON GENOTOUL ?",
            "shortName": "Nextflow/nf-core",
            "description": "This training session is organized by the Genotoul bioinfo platform and aims at learning nf-core workflow submission, error understanding, resuming jobs and ressource reservation. We will present and practice:\r\n\r\nthe Nextflow software\r\nthe nf-core community and pipelines\r\nWhat is a singularity image ?\r\nWhere are installed the nf-core workflows ? Which version do I use ?\r\nHow to run a workflow and which config file is used ?\r\nWhich kind of error I can get ?\r\nHow to resume failed jobs?\r\nHow to handle genome indexes ?\r\nHow to monitor my process and then well configure my workflow ?\r\nHow do you best adjust CPU and RAM reservations?\r\nThis is NOT a bioinformatic training on a particular workflow or a training on how to develop a workflow.\r\n\r\nThis training is focused on practice. It consists of several modules with a large variety of exercises:\r\n\r\nStart at 09:00 am\r\nEnd at 17:00 pm",
            "homepage": "https://bioinfo.genotoul.fr/index.php/events/how-to-run-a-nf-core-nextflow-workflow-on-genotoul-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_0769"
            ],
            "keywords": [
                "Nextflow"
            ],
            "prerequisites": [
                "Linux/Unix",
                "Cluster"
            ],
            "openTo": "Everyone",
            "accessConditions": "",
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            ],
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                    "name": "Genotoul-bioinfo",
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                }
            ],
            "logo_url": "http://bioinfo.genotoul.fr/wp-content/uploads/bioinfo_logo-rvb-petit.png",
            "updated_at": "2025-12-01T11:57:33.124156Z",
            "audienceTypes": [
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            ],
            "audienceRoles": [
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            ],
            "difficultyLevel": "Novice",
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                    "id": 143,
                    "name": "workflows nf-core",
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            ],
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        },
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            "id": 344,
            "name": "Analyses Single Cell RNA-seq (ScRNA-seq) avec R",
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            "description": "Cette formation introduira notamment la librairie Seurat permettant la manipulation et l'analyse de données Single Cell RNA-seq ainsi que la visualisation des résultats d'analyse\r\n\r\n- Rappels des concepts du séquençage Single Cell RNA-seq\r\n- Importation des données Single Cell dans R\r\n- Intégration de données Single Cell multiples\r\n- Quality Check et pré-traitement des données\r\n- Normalisation de données\r\n- Identification de marqueurs\r\n- Clustering et assignation cellulaire\r\n- Analyse différentielle des groupes cellulaires\r\n- Savoir intégrer les données de spatialisation\r\n- Savoir intégrer les données de trajectoire\r\n- Savoir intégrer les données de communication cellulaire\r\n- Savoir intégrer les données d'épigénétique (ATAC-seq)",
            "homepage": "https://cnrsformation.cnrs.fr/analyses-single-cell-rna-seq-scrna-seq-avec-r?axe=176",
            "is_draft": false,
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            "keywords": [
                "Bioinformatics & Biomedical",
                "R Language",
                "R",
                "NGS Sequencing Data Analysis"
            ],
            "prerequisites": [
                "Basic knowledge of R",
                "R programming"
            ],
            "openTo": "Everyone",
            "accessConditions": "Maîtrise du langage R\r\nAvoir suivi le stage \"Langage R : introduction\" ou niveau équivalent.\r\nAfin de vérifier que votre maîtrise du langage R est suffisante pour pouvoir suivre ce stage, nous vous invitons à effectuer et à renvoyer le test téléchargeable\r\nhttps://cnrsformation.cnrs.fr/data/STG_23294_55153.docx",
            "maxParticipants": 12,
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            ],
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            ],
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                    "name": "CBiB",
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                }
            ],
            "logo_url": "https://services.cbib.u-bordeaux.fr/utils/logo_cbib.png",
            "updated_at": "2023-08-31T09:19:56.754683Z",
            "audienceTypes": [
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                "Professional (initial)"
            ],
            "audienceRoles": [
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                "Bioinformaticians"
            ],
            "difficultyLevel": "Intermediate",
            "trainingMaterials": [],
            "learningOutcomes": "- Savoir expertiser et manipuler des données issues d'expériences Single Cell RNA-seq\r\n- Savoir mener une analyse différentielle à de multiples niveaux\r\n- Savoir intégrer des données complémentaires pour l'analyse Single Cell RNA-seq (spatial, trajectoire, cell communication, cell identification...)",
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        },
        {
            "id": 290,
            "name": "NGS data analysis on the command line",
            "shortName": "NGS-analysis-cli",
            "description": "This hands-on course will teach bioinformatic approaches for analyzing Illumina sequencing data. Our goal is to introduce the command line skills you need to make the most of your NGS data. \r\nDuring this 4-day training we will first introduce the Linux environment, shell commands and basic R scripting.  And then we will focus on two NGS data analyses -- small RNA-seq and RNA-seq -- based on published datasets from the model organism Arabidopsis thaliana",
            "homepage": "https://www.ibmp.cnrs.fr/bioinformatics-trainings/",
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                "http://edamontology.org/topic_2269",
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