Handles creating, reading and updating training events.

GET /api/training/?format=api&offset=380&ordering=-audienceRoles
HTTP 200 OK
Allow: GET, POST, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept

{
    "count": 395,
    "next": null,
    "previous": "https://catalogue.france-bioinformatique.fr/api/training/?format=api&limit=20&offset=360&ordering=-audienceRoles",
    "results": [
        {
            "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_0622",
                "http://edamontology.org/topic_0091"
            ],
            "keywords": [],
            "prerequisites": [
                "Master"
            ],
            "openTo": "Internal personnel",
            "accessConditions": "The first sessions are only available for IM2B students.",
            "maxParticipants": 12,
            "contacts": [],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [],
            "organisedByOrganisations": [],
            "organisedByTeams": [
                {
                    "id": 23,
                    "name": "PACA-Bioinfo",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/PACA-Bioinfo/?format=api"
                }
            ],
            "logo_url": null,
            "updated_at": "2022-06-02T11:50:50.812642Z",
            "audienceTypes": [
                "Graduate"
            ],
            "audienceRoles": [
                "Biologists"
            ],
            "difficultyLevel": "Novice",
            "trainingMaterials": [],
            "learningOutcomes": "",
            "hoursPresentations": 1,
            "hoursHandsOn": 5,
            "hoursTotal": 6,
            "personalised": null,
            "event_set": []
        },
        {
            "id": 362,
            "name": "Analyse statistique de données RNA-Seq - Recherche des régions d’intérêt différentiellement exprimées",
            "shortName": "Analyse statistique de données RNA-Seq",
            "description": "Objectifs pédagogiques\r\n* Se sensibiliser aux concepts et méthodes statistiques pour l’analyse de données transcriptomiques de type RNA-Seq.\r\n* Comprendre le matériel et méthodes (normalisation et tests statistiques) d’un article.\r\n* Réaliser une étude transcriptomique avec R dans l’environnement RStudio.\r\n\r\nProgramme\r\n* Planification expérimentale des expériences RNA-Seq (identification des biais, répétitions, biais contrôlables).\r\n* Normalisation et analyse différentielle : recherche de “régions d’intérêt” différentiellement exprimées (modèle linéaire généralisé).\r\n*Prise en compte de la multiplicité des tests.\r\n\r\nLe cours sera illustré par différents exemples. Un jeu de données à deux facteurs sera analysé avec les packages R DESeq2 et edgeR dans l’environnement RStudio.",
            "homepage": "https://documents.migale.inrae.fr/trainings.html",
            "is_draft": false,
            "costs": [
                "Priced"
            ],
            "topics": [
                "http://edamontology.org/topic_0203",
                "http://edamontology.org/topic_3170",
                "http://edamontology.org/topic_3308"
            ],
            "keywords": [
                "Statistical differential analysis",
                "RNA-seq"
            ],
            "prerequisites": [
                "Basic knowledge of R"
            ],
            "openTo": "Everyone",
            "accessConditions": "",
            "maxParticipants": 10,
            "contacts": [
                "https://catalogue.france-bioinformatique.fr/api/userprofile/769/?format=api"
            ],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [],
            "organisedByOrganisations": [
                {
                    "id": 82,
                    "name": "INRAE",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INRAE/?format=api"
                },
                {
                    "id": 88,
                    "name": "BioinfOmics",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/BioinfOmics/?format=api"
                }
            ],
            "organisedByTeams": [
                {
                    "id": 10,
                    "name": "MIGALE",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/MIGALE/?format=api"
                }
            ],
            "logo_url": "https://migale.inrae.fr/sites/default/files/migale-orange_0.png",
            "updated_at": "2024-01-18T14:50:06.093352Z",
            "audienceTypes": [
                "Professional (continued)"
            ],
            "audienceRoles": [
                "Biologists",
                "Bioinformaticians"
            ],
            "difficultyLevel": "Novice",
            "trainingMaterials": [],
            "learningOutcomes": "Objectifs pédagogiques :\r\nSe sensibiliser aux concepts et méthodes statistiques pour l’analyse de données transcriptomiques de type RNA-Seq.\r\nComprendre le matériel et méthodes (normalisation et tests statistiques) d’un article.\r\nRéaliser une étude transcriptomique avec R dans l’environnement RStudio.",
            "hoursPresentations": 4,
            "hoursHandsOn": 8,
            "hoursTotal": 12,
            "personalised": null,
            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/786/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/587/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/695/?format=api"
            ]
        },
        {
            "id": 406,
            "name": "Analyse de données de métabarcoding",
            "shortName": "Métabarcoding",
            "description": "Cette formation est dédiée à l’analyse de données de type “metabarcoding” issues de la technologie de séquençage Illumina. Nous aborderons les différentes étapes bioinformatiques nécessaires pour transformer les données de séquençage brutes en table d’abondances. Nous présenterons également les outils et méthodologies classiquement utilisés pour décrire la diversité observée et comparer les échantillons.\r\n\r\nA l’issue des 4 jours de formation, les stagiaires connaîtront le périmètre, les avantages et limites des analyses de données de séquençage amplicons (métabarcoding). Ils seront capables d’utiliser les outils de FROGS sur les jeux de données de la formation (16S et ITS) et sauront utiliser l’application Easy16S.\r\n\r\nIls seront capables d’identifier les outils et méthodes adaptées au cadre de leurs analyses. S’ils ont en leur possession un jeu de données à analyser, ils sont encouragés à venir avec celui- ci.\r\n\r\nProgramme :\r\n\r\n\r\nAnalyses bioinformatiques sous Galaxy\r\n\r\n    Introduction générale sur les données amplicons\r\n    Présentation et mise en application avec la suite FROGS du nettoyage des données, du clustering, de la détection de chimères, de l’assignation taxonomique et des étapes annexes\r\n    Conclusion, limite des méthodes, outils compagnons\r\n\r\nAnalyses statistiques avec Easy16S\r\n\r\n    Introduction générale\r\n    Import, manipulation et visualisation des données\r\n    Mesure de diversités : Unifrac, Bray-Curtis, etc.\r\n    Ordination et réduction de dimension : MDS\r\n    Clustering et Heatmap\r\n    Comparaison d’échantillons : PERMANOVA, adonis\r\n\r\nMise en application sur données personnelles ou publiques",
            "homepage": "https://documents.migale.inrae.fr/trainings.html",
            "is_draft": false,
            "costs": [
                "Priced"
            ],
            "topics": [
                "http://edamontology.org/topic_3697"
            ],
            "keywords": [
                "Metabarcoding"
            ],
            "prerequisites": [],
            "openTo": "Everyone",
            "accessConditions": "",
            "maxParticipants": 10,
            "contacts": [
                "https://catalogue.france-bioinformatique.fr/api/userprofile/769/?format=api"
            ],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [],
            "organisedByOrganisations": [
                {
                    "id": 82,
                    "name": "INRAE",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INRAE/?format=api"
                },
                {
                    "id": 88,
                    "name": "BioinfOmics",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/BioinfOmics/?format=api"
                }
            ],
            "organisedByTeams": [
                {
                    "id": 10,
                    "name": "MIGALE",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/MIGALE/?format=api"
                }
            ],
            "logo_url": "https://migale.inrae.fr/sites/default/files/migale-orange_0.png",
            "updated_at": "2026-02-12T10:53:42.895487Z",
            "audienceTypes": [
                "Professional (continued)"
            ],
            "audienceRoles": [
                "Biologists",
                "Bioinformaticians"
            ],
            "difficultyLevel": "Novice",
            "trainingMaterials": [],
            "learningOutcomes": "Cette formation est dédiée à l’analyse de données de type “metabarcoding” issues de la technologie de séquençage Illumina. Nous aborderons les différentes étapes bioinformatiques nécessaires pour transformer les données de séquençage brutes en table d’abondances. Nous présenterons également les outils et méthodologies classiquement utilisés pour décrire la diversité observée et comparer les échantillons.\r\n\r\nA l’issue des 4 jours de formation, les stagiaires connaîtront le périmètre, les avantages et limites des analyses de données de séquençage amplicons (métabarcoding). Ils seront capables d’utiliser les outils de FROGS sur les jeux de données de la formation (16S et ITS) et sauront utiliser l’application Easy16S.\r\n\r\nIls seront capables d’identifier les outils et méthodes adaptées au cadre de leurs analyses. S’ils ont en leur possession un jeu de données à analyser, ils sont encouragés à venir avec celui- ci.",
            "hoursPresentations": 12,
            "hoursHandsOn": 12,
            "hoursTotal": 24,
            "personalised": null,
            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/792/?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_0085",
                "http://edamontology.org/topic_3301",
                "http://edamontology.org/topic_0797"
            ],
            "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": [
                "https://catalogue.france-bioinformatique.fr/api/userprofile/90/?format=api"
            ],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [
                {
                    "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": [
                {
                    "id": 9,
                    "name": "MicroScope",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/MicroScope/?format=api"
                }
            ],
            "logo_url": "https://labgem.genoscope.cns.fr/wp-content/uploads/2019/06/MicroScope_logo-300x210.png",
            "updated_at": "2025-12-09T09:10:02.012461Z",
            "audienceTypes": [
                "Undergraduate",
                "Graduate",
                "Professional (continued)"
            ],
            "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/745/?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",
                "https://catalogue.france-bioinformatique.fr/api/event/796/?format=api"
            ]
        },
        {
            "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/",
            "is_draft": false,
            "costs": [
                "Free to academics"
            ],
            "topics": [
                "http://edamontology.org/topic_3170",
                "http://edamontology.org/topic_3168",
                "http://edamontology.org/topic_2269",
                "http://edamontology.org/topic_0102"
            ],
            "keywords": [],
            "prerequisites": [
                "none"
            ],
            "openTo": "Internal personnel",
            "accessConditions": "This training is dedicated to academics working in a laboratory of Unistra/CNRS.",
            "maxParticipants": 12,
            "contacts": [
                "https://catalogue.france-bioinformatique.fr/api/userprofile/124/?format=api"
            ],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [],
            "organisedByOrganisations": [
                {
                    "id": 79,
                    "name": "IBMP",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/IBMP/?format=api"
                }
            ],
            "organisedByTeams": [
                {
                    "id": 14,
                    "name": "BiGEst",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/BiGEst/?format=api"
                }
            ],
            "logo_url": null,
            "updated_at": "2024-01-22T14:51:37.215331Z",
            "audienceTypes": [],
            "audienceRoles": [
                "Biologists",
                "Bioinformaticians"
            ],
            "difficultyLevel": "Novice",
            "trainingMaterials": [],
            "learningOutcomes": "Applied Knowledge (Know-how):\r\n- Basic proficiency at the Linux command line prompt\r\n- Basic proficiency of R (environment, objects, graphs) \r\n- Next generation sequencing (NGS) file formats; reference genomes - Mapping NGS read data to reference genomes (bowtie, samtools)\r\n- Small RNA-seq analysis; epigenomics applications (ShortStack)\r\n- RNA-seq for transcriptomics; differential gene expression analysis (HISAT2, DESeq2) - Data wrangling and visualization in R (Rstudio, ggplot2)",
            "hoursPresentations": 12,
            "hoursHandsOn": 16,
            "hoursTotal": 28,
            "personalised": null,
            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/503/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/504/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/589/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/454/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/660/?format=api"
            ]
        },
        {
            "id": 371,
            "name": "Introduction à l'analyse de données métatranscriptomiques avec Galaxy",
            "shortName": "",
            "description": "L’objectif de cette formation est de se familiariser avec les étapes et les outils d’analyse de données métatranscriptomiques dans le but de comprendre les fonctions d’une communauté microbienne. Nous proposons au personnel non-bioinformaticien de les accompagner dans la prise en main de ces étapes  en utilisant la plateforme de bio-analyse Galaxy. \r\n\r\nAprès une introduction à la métatranscriptomique, une session pratique sur la plateforme Galaxy couvrira comment :\r\n- assigner des taxons à des données de métatranscriptomiques,\r\n- extraire des informations fonctionnelles au sein de données de métatranscriptomiques,\r\n- combiner informations taxonomiques et fonctionnelles pour faciliter la compréhension des fonctions d’une communauté microbienne",
            "homepage": "",
            "is_draft": false,
            "costs": [
                "Free to academics"
            ],
            "topics": [
                "http://edamontology.org/topic_3697",
                "http://edamontology.org/topic_0085",
                "http://edamontology.org/topic_3941",
                "http://edamontology.org/topic_1775"
            ],
            "keywords": [
                "Galaxy"
            ],
            "prerequisites": [
                "Galaxy - Basic usage"
            ],
            "openTo": "Internal personnel",
            "accessConditions": "Formation ouverte au personnel de l’UCA & Associés\r\nAvoir un ordinateur portable et un accès wifi eduroam\r\nAvoir un compte sur la plateforme Galaxy (Faire une demande le cas échéant sur hub.mesocentre.uca.fr)\r\nÊtre familier avec Galaxy",
            "maxParticipants": null,
            "contacts": [
                "https://catalogue.france-bioinformatique.fr/api/userprofile/261/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/userprofile/677/?format=api"
            ],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [
                {
                    "id": 1,
                    "name": "CNRS - IFB",
                    "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/CNRS%20-%20IFB/?format=api"
                },
                {
                    "id": 16,
                    "name": "Université Clermont Auvergne",
                    "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/Universit%C3%A9%20Clermont%20Auvergne/?format=api"
                }
            ],
            "organisedByOrganisations": [
                {
                    "id": 87,
                    "name": "AuBi",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/AuBi/?format=api"
                },
                {
                    "id": 96,
                    "name": "Mésocentre Clermont-Auvergne",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/M%C3%A9socentre%20Clermont-Auvergne/?format=api"
                }
            ],
            "organisedByTeams": [
                {
                    "id": 31,
                    "name": "AuBi",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/AuBi/?format=api"
                }
            ],
            "logo_url": "https://mesocentre.uca.fr/medias/photo/logoaubi-2019minus_1553844844490-jpg?ID_FICHE=41175",
            "updated_at": "2024-02-08T11:22:23.706233Z",
            "audienceTypes": [
                "Undergraduate",
                "Graduate",
                "Professional (initial)",
                "Professional (continued)"
            ],
            "audienceRoles": [
                "Researchers",
                "Life scientists",
                "Biologists"
            ],
            "difficultyLevel": "Novice",
            "trainingMaterials": [
                {
                    "id": 132,
                    "name": "Metatranscriptomics analysis using microbiome RNA-seq data",
                    "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/Metatranscriptomics%20analysis%20using%20microbiome%20RNA-seq%20data/?format=api"
                }
            ],
            "learningOutcomes": "At the end of the tutorial, learners would be able to:\r\n- Choose the best approach to analyze metatranscriptomics data\r\n- Understand the functional microbiome characterization using metatranscriptomic results\r\n- Understand where metatranscriptomics fits in ‘multi-omic’ analysis of microbiomes\r\n- Visualise a community structure",
            "hoursPresentations": 1,
            "hoursHandsOn": 2,
            "hoursTotal": 3,
            "personalised": null,
            "event_set": []
        },
        {
            "id": 275,
            "name": "Single-Cell : Transcriptomics, Spatial and Long reads",
            "shortName": "SincellTE",
            "description": "This workshop focuses on the large-scale study of heterogeneity across individual cells from a genomic, transcriptomic and epigenomic point of view. New technological developments enable the characterization of molecular information at a single cell resolution for large numbers of cells. The high dimensional omics data that these technologies produce raise novel methodological challenges for the analysis. In this regard, dedicated bioinformatics and statistical methods have been developed in order to extract robust information.\r\n\r\nThe workshop aims to provide such methods for engineers and researchers directly involved in functional genomics projects making use of single-cell technologies. A wide range of single cell topics will be covered in lectures, demonstrations and practical classes. Among others, the areas and issues to be addressed will include the choice of the most appropriate single-cell sequencing technology, the experimental design and the bioinformatics and statistical methods and pipelines. For this edition, new courses/practicals will focus on spatial transcriptomics, cell phenotyping and additional multi-omics.\r\n\r\nA wide range of single cell topics will be covered in lectures, demonstrations and practical classes. Among others, the areas and issues to be addressed will include the choice of the most appropriate single-cell sequencing technology, the experimental design and the bioinformatics and statistical methods and pipelines. For this edition, new courses/practicals will focus on spatial transcriptomics, cell phenotyping and additional multi-omics.\r\n\r\nRequirements : Participants must have prior experience on NGS data analysis  with everyday use of R and good knowledge of Unix command line. Before the training, participants will be asked to familiarize themselves with the processing and primary analyses steps of scRNA-seq datasets with provided pedagogic material.\r\n\r\nIt is not necessary to have personal single-cell data to analyse.",
            "homepage": "",
            "is_draft": false,
            "costs": [
                "Priced"
            ],
            "topics": [],
            "keywords": [],
            "prerequisites": [
                "Master",
                "Autre (Diplôme universitaire, école d'ingénieur ...)"
            ],
            "openTo": "Everyone",
            "accessConditions": "Participants must have prior experience on NGS data analysis with everyday use of R and/or Python and good knowledge of Unix command line. Before the training, participants are advised to familiarize themselves with the processing and primary analyses steps of scRNA-seq datasets. \r\nIt is not necessary to have personal single-cell data to analyse.",
            "maxParticipants": 30,
            "contacts": [],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [],
            "organisedByOrganisations": [
                {
                    "id": 4,
                    "name": "IFB - ELIXIR-FR",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/IFB%20-%20ELIXIR-FR/?format=api"
                }
            ],
            "organisedByTeams": [],
            "logo_url": "https://ressources.france-bioinformatique.fr/sites/default/files/sincellTE_logo_0_2.png",
            "updated_at": "2024-03-20T09:31:42.144175Z",
            "audienceTypes": [],
            "audienceRoles": [
                "Researchers",
                "Life scientists",
                "Biologists",
                "Bioinformaticians"
            ],
            "difficultyLevel": "Intermediate",
            "trainingMaterials": [],
            "learningOutcomes": "",
            "hoursPresentations": null,
            "hoursHandsOn": null,
            "hoursTotal": null,
            "personalised": null,
            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/199/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/405/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/422/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/177/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/606/?format=api"
            ]
        },
        {
            "id": 382,
            "name": "Introduction à l'analyse de données transcriptomiques avec Galaxy",
            "shortName": "",
            "description": "L’objectif est de se familiariser avec les étapes d’analyses des données transcriptomiques ou RNA-seq avec référence pour extraire les gènes et fonctions différentiellement exprimés. Nous proposons au personnel non-bioinformaticien de les accompagner dans la prise en main de ces étapes d’analyses en utilisant la plateforme de bio-analyse Galaxy. \r\n\r\n\r\nAprès une introduction à la transcriptomique, une session pratique sur la plateforme Galaxy couvrira comment :\r\n- évaluer la qualité des données transcriptomiques,\r\n- aligner des données transcriptomiques sur un génome de référence,\r\n- estimer le nombre de séquences par gènes,\r\n- construire et faire une analyse d’expression différentielle des gènes\r\n- faire une analyse de l’enrichissement fonctionnel des gènes différentiellement exprimés",
            "homepage": "",
            "is_draft": false,
            "costs": [
                "Free to academics"
            ],
            "topics": [
                "http://edamontology.org/topic_1775",
                "http://edamontology.org/topic_0203",
                "http://edamontology.org/topic_3170",
                "http://edamontology.org/topic_3308"
            ],
            "keywords": [
                "Galaxy",
                "RNA-seq",
                "Transcriptomics (RNA-seq)"
            ],
            "prerequisites": [
                "Galaxy - Basic usage"
            ],
            "openTo": "Internal personnel",
            "accessConditions": "Formation ouverte au personnel de l’UCA & Associés\r\nAvoir un ordinateur portable et un accès wifi eduroam\r\nAvoir un compte sur la plateforme Galaxy (Faire une demande le cas échéant sur hub.mesocentre.uca.fr)\r\nÊtre familier avec Galaxy",
            "maxParticipants": null,
            "contacts": [
                "https://catalogue.france-bioinformatique.fr/api/userprofile/677/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/userprofile/807/?format=api"
            ],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [
                {
                    "id": 1,
                    "name": "CNRS - IFB",
                    "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/CNRS%20-%20IFB/?format=api"
                },
                {
                    "id": 16,
                    "name": "Université Clermont Auvergne",
                    "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/Universit%C3%A9%20Clermont%20Auvergne/?format=api"
                }
            ],
            "organisedByOrganisations": [
                {
                    "id": 87,
                    "name": "AuBi",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/AuBi/?format=api"
                },
                {
                    "id": 96,
                    "name": "Mésocentre Clermont-Auvergne",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/M%C3%A9socentre%20Clermont-Auvergne/?format=api"
                }
            ],
            "organisedByTeams": [
                {
                    "id": 31,
                    "name": "AuBi",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/AuBi/?format=api"
                }
            ],
            "logo_url": "https://mesocentre.uca.fr/medias/photo/logoaubi-2019minus_1553844844490-jpg?ID_FICHE=41175",
            "updated_at": "2024-06-06T08:06:54.982689Z",
            "audienceTypes": [
                "Undergraduate",
                "Graduate",
                "Professional (initial)",
                "Professional (continued)"
            ],
            "audienceRoles": [
                "Researchers",
                "Life scientists",
                "Biologists"
            ],
            "difficultyLevel": "Novice",
            "trainingMaterials": [
                {
                    "id": 144,
                    "name": "Reference-based RNA-Seq data analysis with Galaxy",
                    "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/Reference-based%20RNA-Seq%20data%20analysis%20with%20Galaxy/?format=api"
                },
                {
                    "id": 145,
                    "name": "Introduction to Transcriptomics",
                    "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/Introduction%20to%20Transcriptomics/?format=api"
                }
            ],
            "learningOutcomes": "At the end of the tutorial, learners would be able to:\r\n- Check a sequence quality report generated by FastQC for RNA-Seq data\r\n- Explain the principle and specificity of mapping of RNA-Seq data to an eukaryotic reference genome\r\n- Select and run a state of the art mapping tool for RNA-Seq data\r\n- Evaluate the quality of mapping results\r\n- Describe the process to estimate the library strandness\r\n- Estimate the number of reads per genes\r\n- Explain the count normalization to perform before sample comparison\r\n- Construct and run a differential gene expression analysis\r\n- Analyze the DESeq2 output to identify, annotate and visualize differentially expressed genes\r\n- Perform a gene ontology enrichment analysis\r\n- Perform and visualize an enrichment analysis for KEGG pathways",
            "hoursPresentations": 1,
            "hoursHandsOn": 7,
            "hoursTotal": 8,
            "personalised": null,
            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/637/?format=api"
            ]
        },
        {
            "id": 372,
            "name": "Introduction à l'analyse d’images avec Galaxy",
            "shortName": "",
            "description": "L’objectif de cette formation est de se familiariser avec les premières étapes à l’analyse d’images. Nous proposons au personnel non-bioinformaticien de les accompagner dans la prise en main des ces étapes d’analyses en utilisant la plateforme de bio-analyse Galaxy. \r\n\r\nAprès une introduction à l’analyse d’images, une session pratique sur la plateforme Galaxy couvrira comment :\r\n- extraire des métadonnées d’une image,\r\n- convertir, filtrer et segmenter une image",
            "homepage": "",
            "is_draft": false,
            "costs": [
                "Free to academics"
            ],
            "topics": [
                "http://edamontology.org/topic_3383",
                "http://edamontology.org/topic_3382"
            ],
            "keywords": [
                "Galaxy"
            ],
            "prerequisites": [
                "Galaxy - Basic usage"
            ],
            "openTo": "Internal personnel",
            "accessConditions": "Formation ouverte au personnel de l’UCA & Associés\r\nAvoir un ordinateur portable et un accès wifi eduroam\r\nAvoir un compte sur la plateforme Galaxy (Faire une demande le cas échéant sur hub.mesocentre.uca.fr)\r\nÊtre familier avec Galaxy",
            "maxParticipants": null,
            "contacts": [
                "https://catalogue.france-bioinformatique.fr/api/userprofile/261/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/userprofile/677/?format=api"
            ],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [
                {
                    "id": 1,
                    "name": "CNRS - IFB",
                    "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/CNRS%20-%20IFB/?format=api"
                },
                {
                    "id": 16,
                    "name": "Université Clermont Auvergne",
                    "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/Universit%C3%A9%20Clermont%20Auvergne/?format=api"
                }
            ],
            "organisedByOrganisations": [
                {
                    "id": 87,
                    "name": "AuBi",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/AuBi/?format=api"
                },
                {
                    "id": 96,
                    "name": "Mésocentre Clermont-Auvergne",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/M%C3%A9socentre%20Clermont-Auvergne/?format=api"
                }
            ],
            "organisedByTeams": [
                {
                    "id": 31,
                    "name": "AuBi",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/AuBi/?format=api"
                }
            ],
            "logo_url": "https://mesocentre.uca.fr/medias/photo/logoaubi-2019minus_1553844844490-jpg?ID_FICHE=41175",
            "updated_at": "2024-02-08T11:25:36.663764Z",
            "audienceTypes": [
                "Undergraduate",
                "Graduate",
                "Professional (initial)",
                "Professional (continued)"
            ],
            "audienceRoles": [
                "Researchers",
                "Life scientists",
                "Biologists"
            ],
            "difficultyLevel": "Novice",
            "trainingMaterials": [
                {
                    "id": 133,
                    "name": "Introduction to image analysis using Galaxy",
                    "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/Introduction%20to%20image%20analysis%20using%20Galaxy/?format=api"
                }
            ],
            "learningOutcomes": "At the end of the tutorial, learners would be able to:\r\n- How to handle images in Galaxy.\r\n- How to perform basic image processing in Galaxy",
            "hoursPresentations": 1,
            "hoursHandsOn": 2,
            "hoursTotal": 3,
            "personalised": null,
            "event_set": []
        },
        {
            "id": 384,
            "name": "EBAII - Ecole de Bioinformatique niveau intermédiaire",
            "shortName": "EBAII N2",
            "description": "Objectifs: L’école s’articulera autour de trois ateliers thématiques en session parallèle (RNA-seq, ChIP-seq, variants DNA-seq), et abordera la visualisation et l’intégration des données. \r\n\r\nEnvironnement de travail: L’ensemble de la formation reposera sur l’utilisation de commandes en ligne (terminal Linux) et du langage R. \r\n\r\nPrérequis: Les candidats doivent avoir acquis les compétences enseignées durant l’école de niveau débutant: un niveau de base en ligne de commande, R, et (au choix) RNA-seq, ChIP-seq ou variants DNA-seq.",
            "homepage": "",
            "is_draft": false,
            "costs": [
                "Priced"
            ],
            "topics": [
                "http://edamontology.org/topic_3391",
                "http://edamontology.org/topic_3366",
                "http://edamontology.org/topic_0092",
                "http://edamontology.org/topic_3168",
                "http://edamontology.org/topic_0091"
            ],
            "keywords": [
                "Biostatistics",
                "Sequence analysis",
                "NGS Sequencing Data Analysis"
            ],
            "prerequisites": [],
            "openTo": "Everyone",
            "accessConditions": "La formation s’adresse à des biologistes directement impliqués dans des projets “Next Generation Sequencing” (NGS)  avec un niveau de base en ligne de commande, R, et (au choix) RNA-seq, ChIP-seq ou variants DNA-seq.",
            "maxParticipants": null,
            "contacts": [],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [],
            "organisedByOrganisations": [],
            "organisedByTeams": [],
            "logo_url": "https://www.sb-roscoff.fr/sites/www.sb-roscoff.fr/files/styles/large/public/images/station-biologique-roscoff-roscoff-4404.jpg",
            "updated_at": "2024-12-05T07:33:48.573507Z",
            "audienceTypes": [],
            "audienceRoles": [
                "Biologists"
            ],
            "difficultyLevel": "",
            "trainingMaterials": [],
            "learningOutcomes": "",
            "hoursPresentations": null,
            "hoursHandsOn": null,
            "hoursTotal": null,
            "personalised": null,
            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/644/?format=api"
            ]
        },
        {
            "id": 375,
            "name": "RNASeq Analysis",
            "shortName": "RNASeq Analysis",
            "description": "Objectives\r\n- Understand the key steps in RNASeq data analysis for a differential expression study\r\n- Know how to perform command-line analysis using Snakemake.\r\n\r\nPedagogical Content\r\nDay 1\r\n- Principle of RNASeq technology: objectives and experimental design.\r\n- Data quality assessment (FastQC, MultiQC).\r\n- Sequence alignment to a reference genome (STAR).\r\n\r\nDay 2\r\n- Differential gene expression analysis (HTSeqCount, DESeq2).\r\n- Functional annotation (GO, Kegg).\r\n- Using the Snakemake workflow system.\r\n- Comparison between RNASeq and 3’SRP methods.\r\n\r\nThe theoretical part is followed by a pipeline run step-by-step on a test dataset. \r\nIt will be possible to start an analysis on your own data.",
            "homepage": "https://pf-bird.univ-nantes.fr/training/rnaseq/",
            "is_draft": false,
            "costs": [
                "Priced"
            ],
            "topics": [],
            "keywords": [],
            "prerequisites": [],
            "openTo": "Everyone",
            "accessConditions": "- Be comfortable with basic Linux commands or have completed the training course “Introduction to the command-line interface.”\r\n- Be familiar with the use of a computing cluster, conda/mamba et snakemake or have completed the training course “Best practices in bioinformatics.”",
            "maxParticipants": 12,
            "contacts": [],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [],
            "organisedByOrganisations": [],
            "organisedByTeams": [
                {
                    "id": 16,
                    "name": "BiRD",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/BiRD/?format=api"
                }
            ],
            "logo_url": "https://bird.univ-nantes.io/website/images/logo/logo.svg",
            "updated_at": "2026-03-02T16:30:29.225935Z",
            "audienceTypes": [
                "Professional (continued)"
            ],
            "audienceRoles": [
                "Life scientists",
                "Biologists",
                "Bioinformaticians"
            ],
            "difficultyLevel": "",
            "trainingMaterials": [],
            "learningOutcomes": "",
            "hoursPresentations": 7,
            "hoursHandsOn": 7,
            "hoursTotal": 14,
            "personalised": null,
            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/746/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/603/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/640/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/812/?format=api"
            ]
        },
        {
            "id": 366,
            "name": "Initiation à l’utilisation de la plateforme de bio-analyse Galaxy",
            "shortName": "",
            "description": "L’objectif est de se familiariser avec l’interface utilisateur de Galaxy. \r\n\r\nAprès une introduction à Galaxy, une session pratique sur la plateforme Galaxy couvrira comment :\r\n- Importer des données\r\n- Identifier des outils\r\n- Faire une analyse\r\n- Gérer un historique\r\n- Créer un workflow",
            "homepage": "",
            "is_draft": false,
            "costs": [
                "Free to academics"
            ],
            "topics": [
                "http://edamontology.org/topic_0091"
            ],
            "keywords": [
                "Galaxy"
            ],
            "prerequisites": [],
            "openTo": "Internal personnel",
            "accessConditions": "Formation ouverte au personnel de l’UCA & Associés\r\nAvoir un ordinateur portable et un accès wifi eduroam\r\nAvoir un compte sur la plateforme Galaxy (Faire une demande le cas échéant sur hub.mesocentre.uca.fr)",
            "maxParticipants": null,
            "contacts": [
                "https://catalogue.france-bioinformatique.fr/api/userprofile/261/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/userprofile/677/?format=api"
            ],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [
                {
                    "id": 1,
                    "name": "CNRS - IFB",
                    "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/CNRS%20-%20IFB/?format=api"
                },
                {
                    "id": 16,
                    "name": "Université Clermont Auvergne",
                    "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/Universit%C3%A9%20Clermont%20Auvergne/?format=api"
                }
            ],
            "organisedByOrganisations": [
                {
                    "id": 87,
                    "name": "AuBi",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/AuBi/?format=api"
                },
                {
                    "id": 96,
                    "name": "Mésocentre Clermont-Auvergne",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/M%C3%A9socentre%20Clermont-Auvergne/?format=api"
                }
            ],
            "organisedByTeams": [
                {
                    "id": 31,
                    "name": "AuBi",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/AuBi/?format=api"
                }
            ],
            "logo_url": "https://mesocentre.uca.fr/medias/photo/logoaubi-2019minus_1553844844490-jpg?ID_FICHE=41175",
            "updated_at": "2024-02-08T10:47:23.782242Z",
            "audienceTypes": [
                "Graduate",
                "Professional (initial)",
                "Professional (continued)",
                "Undergraduate"
            ],
            "audienceRoles": [
                "Researchers",
                "Life scientists",
                "Biologists"
            ],
            "difficultyLevel": "Novice",
            "trainingMaterials": [
                {
                    "id": 126,
                    "name": "Galaxy 101 for everyone",
                    "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/Galaxy%20101%20for%20everyone/?format=api"
                }
            ],
            "learningOutcomes": "At the end of the tutorial, learners would be able to:\r\n- Assess short reads FASTQ quality using FASTQE 🧬😎 and FastQC\r\n- Assess long reads FASTQ quality using Nanoplot and PycoQC\r\n- Perform quality correction with Cutadapt (short reads)\r\n-  Summarise quality metrics MultiQC\r\n- Process single-end and paired-end data\r\n- Define what mapping is\r\n- Perform mapping of reads on a reference genome\r\n- Evaluate the mapping output",
            "hoursPresentations": 1,
            "hoursHandsOn": 2,
            "hoursTotal": 3,
            "personalised": null,
            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/592/?format=api"
            ]
        },
        {
            "id": 412,
            "name": "Construction and analysis of eukaryotic pangenome graphs",
            "shortName": "",
            "description": "This training session is organized by the Genotoul-Bioinfo platform. This 2 days long course is dedicated to the construction and the analysis of eukaryotic pangenome graphs.\r\n\r\nWe will first present the concept of graph-based pangenome, then build one. We will then apply several tools for its analysis: use annotation, call variants, extract sub-graphs, visualize the graph, map reads, genotype individuals, and perform a GWAS on the graph. The different formats will also be presented.\r\n\r\nBy the end of the course, trainees will be familiar with the topic, and able to run the major tools made to build an exploit a pangenome graph.",
            "homepage": "https://bioinfo.genotoul.fr/index.php/events/pangenome/",
            "is_draft": false,
            "costs": [
                "Non-academic for non-academic: 1100€ + 20% taxes (TVA)",
                "INRAE for INRAE's staff: 300 € no VAT charged",
                "Academic non-INRAE for academic but non-INRAE: 340 € + 20% taxes (TVA)"
            ],
            "topics": [
                "http://edamontology.org/topic_3796",
                "http://edamontology.org/topic_0625"
            ],
            "keywords": [
                "Pangenomic"
            ],
            "prerequisites": [
                "Linux/Unix",
                "Cluster"
            ],
            "openTo": "Everyone",
            "accessConditions": "",
            "maxParticipants": 12,
            "contacts": [
                "https://catalogue.france-bioinformatique.fr/api/userprofile/642/?format=api"
            ],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [],
            "organisedByOrganisations": [
                {
                    "id": 82,
                    "name": "INRAE",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INRAE/?format=api"
                },
                {
                    "id": 88,
                    "name": "BioinfOmics",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/BioinfOmics/?format=api"
                },
                {
                    "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"
                }
            ],
            "organisedByTeams": [
                {
                    "id": 22,
                    "name": "Genotoul-bioinfo",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/Genotoul-bioinfo/?format=api"
                }
            ],
            "logo_url": "https://bioinfo.genotoul.fr/wp-content/uploads/bioinfo_logo-rvb-petit.png",
            "updated_at": "2026-04-20T08:06:46.497837Z",
            "audienceTypes": [
                "Professional (continued)"
            ],
            "audienceRoles": [
                "Life scientists",
                "Biologists",
                "Bioinformaticians"
            ],
            "difficultyLevel": "Intermediate",
            "trainingMaterials": [],
            "learningOutcomes": "",
            "hoursPresentations": 3,
            "hoursHandsOn": 15,
            "hoursTotal": 18,
            "personalised": null,
            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/799/?format=api"
            ]
        },
        {
            "id": 367,
            "name": "Introduction à l'analyse de données de séquençage avec contrôle qualité et alignement sur un génome de référence avec Galaxy",
            "shortName": "",
            "description": "L’objectif de cette formation est de se familiariser avec les premières étapes communes à toutes les analyses de données de séquençage : le contrôle qualité des données et l’alignement sur un génome de référence. Nous proposons au personnel non-bioinformaticien de les accompagner dans la prise en main des ces étapes d’analyses en utilisant la plateforme de bio-analyse Galaxy. \r\n\r\nAprès une introduction aux données de séquençage, une session pratique sur la plateforme Galaxy couvrira comment :\r\n- évaluer la qualité de données de séquençage,\r\n- améliorer la qualité de données de séquençage\r\n- aligner des données sur un génome de référence",
            "homepage": "",
            "is_draft": false,
            "costs": [
                "Free to academics"
            ],
            "topics": [
                "http://edamontology.org/topic_0091",
                "http://edamontology.org/topic_0102"
            ],
            "keywords": [
                "Quality Control",
                "Galaxy",
                "Mapping"
            ],
            "prerequisites": [
                "Galaxy - Basic usage"
            ],
            "openTo": "Internal personnel",
            "accessConditions": "Formation ouverte au personnel de l’UCA & Associés\r\nAvoir un ordinateur portable et un accès wifi eduroam\r\nAvoir un compte sur la plateforme Galaxy (Faire une demande le cas échéant sur hub.mesocentre.uca.fr)\r\nÊtre familier avec Galaxy",
            "maxParticipants": null,
            "contacts": [
                "https://catalogue.france-bioinformatique.fr/api/userprofile/261/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/userprofile/677/?format=api"
            ],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [
                {
                    "id": 1,
                    "name": "CNRS - IFB",
                    "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/CNRS%20-%20IFB/?format=api"
                },
                {
                    "id": 16,
                    "name": "Université Clermont Auvergne",
                    "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/Universit%C3%A9%20Clermont%20Auvergne/?format=api"
                }
            ],
            "organisedByOrganisations": [
                {
                    "id": 87,
                    "name": "AuBi",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/AuBi/?format=api"
                },
                {
                    "id": 96,
                    "name": "Mésocentre Clermont-Auvergne",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/M%C3%A9socentre%20Clermont-Auvergne/?format=api"
                }
            ],
            "organisedByTeams": [
                {
                    "id": 31,
                    "name": "AuBi",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/AuBi/?format=api"
                }
            ],
            "logo_url": "https://mesocentre.uca.fr/medias/photo/logoaubi-2019minus_1553844844490-jpg?ID_FICHE=41175",
            "updated_at": "2024-02-08T11:22:59.733596Z",
            "audienceTypes": [
                "Undergraduate",
                "Graduate",
                "Professional (initial)",
                "Professional (continued)"
            ],
            "audienceRoles": [
                "Researchers",
                "Life scientists",
                "Biologists"
            ],
            "difficultyLevel": "Novice",
            "trainingMaterials": [
                {
                    "id": 128,
                    "name": "Mapping with Galaxy",
                    "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/Mapping%20with%20Galaxy/?format=api"
                },
                {
                    "id": 127,
                    "name": "Quality Control with Galaxy",
                    "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/Quality%20Control%20with%20Galaxy/?format=api"
                }
            ],
            "learningOutcomes": "At the end of the tutorial, learners would be able to:\r\n- Assess short reads FASTQ quality using FASTQE 🧬😎 and FastQC\r\n- Assess long reads FASTQ quality using Nanoplot and PycoQC\r\n- Perform quality correction with Cutadapt (short reads)\r\n-  Summarise quality metrics MultiQC\r\n- Process single-end and paired-end data\r\n- Define what mapping is\r\n- Perform mapping of reads on a reference genome\r\n- Evaluate the mapping output",
            "hoursPresentations": 1,
            "hoursHandsOn": 2,
            "hoursTotal": 3,
            "personalised": null,
            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/593/?format=api"
            ]
        },
        {
            "id": 405,
            "name": "Annotation et comparaison de génomes bactériens",
            "shortName": "Annotation et comparaison de génomes bactériens",
            "description": "Connaître les concepts et les principales méthodes bioinformatiques pour annoter automatiquement et comparer un jeu de données de génomes bactériens. Construire et évaluer la qualité d’un jeu de données publiques. Évaluer la qualité et annoter automatiquement un jeu de données. Savoir mettre en oeuvre une comparaison de génomes et en interpréter les résultats.\r\n\r\nProgramme :\r\n\r\n* Construction d’un jeu de données :\r\n        Téléchargement de données publiques\r\n        Evaluation de la qualité d’un jeu de données\r\n\r\n* Principes et mise en œuvre d’une annotation automatique d’un génome bactérien\r\n\r\n * Caractérisation de la diversité génomique\r\n\r\n * Construction de pangénomes\r\n\r\n * Analyse des résultats :\r\n        Résultats et métriques d’un pangénome\r\n        Notions élémentaires de phylogénomique\r\n        Visualisation et interprétation des résultats\r\n\r\n * Mise en pratique sur un jeu de données bactériens, utilisation des logiciels dRep, Quast, Bakta et PPanGGOLiN sous Galaxy.",
            "homepage": "https://documents.migale.inrae.fr/trainings.html",
            "is_draft": false,
            "costs": [
                "Priced"
            ],
            "topics": [
                "http://edamontology.org/topic_3299",
                "http://edamontology.org/topic_0622",
                "http://edamontology.org/topic_0797"
            ],
            "keywords": [
                "Genome annotation",
                "Comparative genomics"
            ],
            "prerequisites": [],
            "openTo": "Everyone",
            "accessConditions": "",
            "maxParticipants": 10,
            "contacts": [
                "https://catalogue.france-bioinformatique.fr/api/userprofile/769/?format=api"
            ],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [],
            "organisedByOrganisations": [
                {
                    "id": 82,
                    "name": "INRAE",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INRAE/?format=api"
                },
                {
                    "id": 88,
                    "name": "BioinfOmics",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/BioinfOmics/?format=api"
                }
            ],
            "organisedByTeams": [
                {
                    "id": 10,
                    "name": "MIGALE",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/MIGALE/?format=api"
                }
            ],
            "logo_url": "https://migale.inrae.fr/sites/default/files/migale-orange_0.png",
            "updated_at": "2026-02-12T10:45:53.661422Z",
            "audienceTypes": [
                "Professional (continued)"
            ],
            "audienceRoles": [
                "Biologists",
                "Bioinformaticians"
            ],
            "difficultyLevel": "",
            "trainingMaterials": [],
            "learningOutcomes": "Connaître les concepts et les principales méthodes bioinformatiques pour annoter automatiquement et comparer un jeu de données de génomes bactériens. Construire et évaluer la qualité d’un jeu de données publiques. Évaluer la qualité et annoter automatiquement un jeu de données. Savoir mettre en oeuvre une comparaison de génomes et en interpréter les résultats.",
            "hoursPresentations": 6,
            "hoursHandsOn": 6,
            "hoursTotal": 12,
            "personalised": null,
            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/791/?format=api"
            ]
        },
        {
            "id": 344,
            "name": "Analyses Single Cell RNA-seq (ScRNA-seq) avec R",
            "shortName": "",
            "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,
            "costs": [],
            "topics": [],
            "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,
            "contacts": [
                "https://catalogue.france-bioinformatique.fr/api/userprofile/154/?format=api"
            ],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [
                {
                    "id": 6,
                    "name": "CNRS formation entreprise",
                    "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/CNRS%20formation%20entreprise/?format=api"
                }
            ],
            "organisedByOrganisations": [
                {
                    "id": 1,
                    "name": "CNRS formation entreprises",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/CNRS%20formation%20entreprises/?format=api"
                }
            ],
            "organisedByTeams": [
                {
                    "id": 6,
                    "name": "CBiB",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/CBiB/?format=api"
                }
            ],
            "logo_url": "https://services.cbib.u-bordeaux.fr/utils/logo_cbib.png",
            "updated_at": "2023-08-31T09:19:56.754683Z",
            "audienceTypes": [
                "Graduate",
                "Professional (initial)"
            ],
            "audienceRoles": [
                "Biologists",
                "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...)",
            "hoursPresentations": null,
            "hoursHandsOn": null,
            "hoursTotal": null,
            "personalised": null,
            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/650/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/653/?format=api"
            ]
        },
        {
            "id": 287,
            "name": "Introduction to Oxford Nanopore Technology data analyses",
            "shortName": "Introduction to ONT data analyses",
            "description": "This course offers an introduction to ONT data analysis. It includes 5 issues: basecalling, reads quality control, assemblies and polishing/correction, contig quality and structural variants detection.",
            "homepage": "https://southgreenplatform.github.io/trainings//ont/",
            "is_draft": false,
            "costs": [
                "Free"
            ],
            "topics": [
                "http://edamontology.org/topic_3673",
                "http://edamontology.org/topic_0196",
                "http://edamontology.org/topic_3168"
            ],
            "keywords": [],
            "prerequisites": [
                "Linux and knowledge of NGS formats"
            ],
            "openTo": "Everyone",
            "accessConditions": "",
            "maxParticipants": 15,
            "contacts": [],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [],
            "organisedByOrganisations": [],
            "organisedByTeams": [
                {
                    "id": 24,
                    "name": "South Green",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/South%20Green/?format=api"
                }
            ],
            "logo_url": "https://southgreenplatform.github.io/trainings//images/southgreenlong.png",
            "updated_at": "2023-01-24T10:21:58.467251Z",
            "audienceTypes": [
                "Professional (initial)"
            ],
            "audienceRoles": [
                "Life scientists",
                "Biologists"
            ],
            "difficultyLevel": "Novice",
            "trainingMaterials": [
                {
                    "id": 1,
                    "name": "SG-ONT-slides",
                    "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/SG-ONT-slides/?format=api"
                }
            ],
            "learningOutcomes": "* Understanding limits and advantages of ONT technology\r\n* Manipulating ONT data on a virtual machine on jupyter environment\r\n* Handling mapping, assembly, polishing tools and be able to analyse your own data\r\n* Detecting structural variations using long reads",
            "hoursPresentations": 6,
            "hoursHandsOn": 6,
            "hoursTotal": 12,
            "personalised": null,
            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/441/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/450/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/562/?format=api"
            ]
        },
        {
            "id": 303,
            "name": "Tools for phylogenetic analysis",
            "shortName": "",
            "description": "You will learn How to find homologs, make multiple alignments, reconstruct the phylogeny, visualize the tree.\r\n\r\nAt the end of the workshop, you will be able to use web tools to reconstruct accurate phylogenies.\r\n\r\nUnless all participants speak French, the course will be taught in English.",
            "homepage": "https://pliniuscursus.univ-amu.fr/formation/tools-for-phylogenetic-analysis/",
            "is_draft": false,
            "costs": [
                "Free to academics"
            ],
            "topics": [
                "http://edamontology.org/topic_0084"
            ],
            "keywords": [],
            "prerequisites": [
                "Master"
            ],
            "openTo": "Internal personnel",
            "accessConditions": "The first sessions are only available for IM2B students.",
            "maxParticipants": 10,
            "contacts": [],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [],
            "organisedByOrganisations": [
                {
                    "id": 38,
                    "name": "IGS - Laboratoire Information Génomique et Structurale",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/IGS%20-%20Laboratoire%20Information%20G%C3%A9nomique%20et%20Structurale/?format=api"
                }
            ],
            "organisedByTeams": [
                {
                    "id": 23,
                    "name": "PACA-Bioinfo",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/PACA-Bioinfo/?format=api"
                }
            ],
            "logo_url": null,
            "updated_at": "2022-06-02T11:50:50.812642Z",
            "audienceTypes": [
                "Graduate"
            ],
            "audienceRoles": [
                "Biologists"
            ],
            "difficultyLevel": "Novice",
            "trainingMaterials": [],
            "learningOutcomes": "",
            "hoursPresentations": 1,
            "hoursHandsOn": 5,
            "hoursTotal": 6,
            "personalised": null,
            "event_set": []
        },
        {
            "id": 302,
            "name": "Initiation à la ligne de commande",
            "shortName": "",
            "description": "L’objectif de cette formation est de se familiariser à l’utilisation de la ligne de commande pour un usage sur un cluster de\r\ncalcul afin d’acquérir les bases pour le traitement de données biologiques.\r\nPrésentation de l’infrastructure du cluster de calcul du Mésocentre Clermont Auvergne.\r\nIntroduction à l’environnement Linux.\r\nInitiation à un langage de scripting avec le shell Bash.\r\nManipulation en ligne de commande de fichiers de données d'origine biologique.\r\nComment se connecter au serveur de calcul.\r\nApprentissage du langage informatique Bash et comment naviguer dans un environnement Linux.\r\nExercices pratiques de saisie de commandes sur un terminal sans interface graphique.\r\nApprentissage de la gestion de fichiers, comment les créer, gérer les droits d’accès, les manipuler et les transférer sur le\r\ncluster de calcul ou les récupérer sur son poste de travail local.",
            "homepage": "https://mesocentre.uca.fr/",
            "is_draft": false,
            "costs": [
                "Free to academics"
            ],
            "topics": [
                "http://edamontology.org/topic_0605",
                "http://edamontology.org/topic_0091"
            ],
            "keywords": [],
            "prerequisites": [
                "Licence"
            ],
            "openTo": "Everyone",
            "accessConditions": "Avoir un compte sur le cluster de calcul du Mésocentre Clermont Auvergne (faire une demande le cas échéant sur le site\r\nhttps://hub.mesocentre.uca.fr)\r\nVENIR AVEC UN ORDINATEUR PORTABLE muni d’une connexion à Eduroam opérationnelle.",
            "maxParticipants": 10,
            "contacts": [
                "https://catalogue.france-bioinformatique.fr/api/userprofile/261/?format=api"
            ],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [],
            "organisedByOrganisations": [
                {
                    "id": 45,
                    "name": "UMR 454 MEDIS INRA-Université Clermont Auvergne",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/UMR%20454%20MEDIS%20INRA-Universit%C3%A9%20Clermont%20Auvergne/?format=api"
                }
            ],
            "organisedByTeams": [
                {
                    "id": 31,
                    "name": "AuBi",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/AuBi/?format=api"
                }
            ],
            "logo_url": "https://mesocentre.uca.fr/medias/photo/logoaubi-2019minus_1553844844490-jpg?ID_FICHE=41175",
            "updated_at": "2025-02-17T12:44:35.172676Z",
            "audienceTypes": [
                "Professional (initial)"
            ],
            "audienceRoles": [
                "Life scientists",
                "Biologists"
            ],
            "difficultyLevel": "Novice",
            "trainingMaterials": [],
            "learningOutcomes": "",
            "hoursPresentations": 2,
            "hoursHandsOn": 3,
            "hoursTotal": 6,
            "personalised": false,
            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/482/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/749/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/750/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/615/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/event/707/?format=api"
            ]
        },
        {
            "id": 368,
            "name": "Introduction à l'annotation de génomes bactériens avec Galaxy",
            "shortName": "",
            "description": "L’objectif est cette formation de se familiariser avec les étapes et les outils pour annoter des génomes bactériens. Nous proposons au personnel non-bioinformaticien de les accompagner dans la prise en main de l’annotation de génomes bactériens en utilisant la plateforme de bio-analyse Galaxy. \r\n\r\nAprès une introduction à l’annotation de génomes bactériens, une session pratique sur la plateforme Galaxy couvrira comment :\r\n- faire tourner une série d’outils pour annoter un génome bactérien avec différents éléments génomiques,\r\n- évaluer l’annotation\r\n- visualiser un génome bactérien et ses annotations",
            "homepage": "",
            "is_draft": false,
            "costs": [
                "Free to academics"
            ],
            "topics": [
                "http://edamontology.org/topic_3301",
                "http://edamontology.org/topic_0097",
                "http://edamontology.org/topic_0219",
                "http://edamontology.org/topic_0622"
            ],
            "keywords": [
                "Bacterial isolate",
                "Galaxy",
                "Structural and functional annotation of genomes"
            ],
            "prerequisites": [
                "Galaxy - Basic usage"
            ],
            "openTo": "Internal personnel",
            "accessConditions": "Formation ouverte au personnel de l’UCA & Associés\r\nAvoir un ordinateur portable et un accès wifi eduroam\r\nAvoir un compte sur la plateforme Galaxy (Faire une demande le cas échéant sur hub.mesocentre.uca.fr)\r\nÊtre familier avec Galaxy",
            "maxParticipants": null,
            "contacts": [
                "https://catalogue.france-bioinformatique.fr/api/userprofile/261/?format=api",
                "https://catalogue.france-bioinformatique.fr/api/userprofile/677/?format=api"
            ],
            "elixirPlatforms": [],
            "communities": [],
            "sponsoredBy": [
                {
                    "id": 1,
                    "name": "CNRS - IFB",
                    "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/CNRS%20-%20IFB/?format=api"
                },
                {
                    "id": 16,
                    "name": "Université Clermont Auvergne",
                    "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/Universit%C3%A9%20Clermont%20Auvergne/?format=api"
                }
            ],
            "organisedByOrganisations": [
                {
                    "id": 87,
                    "name": "AuBi",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/AuBi/?format=api"
                },
                {
                    "id": 96,
                    "name": "Mésocentre Clermont-Auvergne",
                    "url": "https://catalogue.france-bioinformatique.fr/api/organisation/M%C3%A9socentre%20Clermont-Auvergne/?format=api"
                }
            ],
            "organisedByTeams": [
                {
                    "id": 31,
                    "name": "AuBi",
                    "url": "https://catalogue.france-bioinformatique.fr/api/team/AuBi/?format=api"
                }
            ],
            "logo_url": "https://mesocentre.uca.fr/medias/photo/logoaubi-2019minus_1553844844490-jpg?ID_FICHE=41175",
            "updated_at": "2024-02-08T11:22:51.682232Z",
            "audienceTypes": [
                "Undergraduate",
                "Graduate",
                "Professional (initial)",
                "Professional (continued)"
            ],
            "audienceRoles": [
                "Researchers",
                "Life scientists",
                "Biologists"
            ],
            "difficultyLevel": "Novice",
            "trainingMaterials": [
                {
                    "id": 129,
                    "name": "Bacterial Genome Annotation",
                    "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/Bacterial%20Genome%20Annotation/?format=api"
                }
            ],
            "learningOutcomes": "At the end of the tutorial, learners would be able to:\r\n- Run a series of tools to annotate a draft bacterial genome for different types of genomic components\r\n- Evaluate the annotation\r\n- Process the outputs to format them for visualization needs\r\n- Visualize a draft bacterial genome and its annotations",
            "hoursPresentations": 1,
            "hoursHandsOn": 2,
            "hoursTotal": 3,
            "personalised": null,
            "event_set": [
                "https://catalogue.france-bioinformatique.fr/api/event/598/?format=api"
            ]
        }
    ]
}