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            "name": "Analyse de données de métabarcoding : 2025",
            "shortName": "Analyse de données de 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\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).\r\nIls seront capables d’utiliser les outils de FROGS sur les jeux de données de la formation (16S et ITS).\r\nIls seront capables d’identifier les outils et méthodes adaptées au cadre de leurs analyses.\r\nS’ils ont en leur possession un jeu de données à analyser, ils sont encouragés à venir avec celui- ci.",
            "homepage": "https://migale.inrae.fr/trainings/",
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            "updated_at": "2025-01-23T15:50:14.223205Z",
            "type": "Training course",
            "start_date": "2025-06-23",
            "end_date": "2025-06-26",
            "venue": "Access to the INRAE center reception\r\n By car\r\n\r\n    Take the N118 from the Paris rotary Porte de Saint-Cloud > Pont de Sèvres > Follow direction Bordeaux/Nantes – take exit 6A Jouy-en-Josas/Bièvres\r\n    Take the N12 from Plaisir > Follow direction Paris exit 1 towards the D53\r\n    Take the A12 Rambouillet > Jouy – take exit 2 via the D446\r\n\r\n By the RER (train to the suburbs)\r\n\r\nRER C Line: Get off at the Jouy-en-Josas station. The research center is a 15 minute walk (you must walk towards the town hall (Mairie de Jouy).\r\n\r\n    From Chatelet-Les Halles, take the RER B line until the Massy-Palaiseau station (32 min.) then take the RER C line CIME train (14 min.)\r\n    From Versailles-Chantier RER C station take the VICK or VITY train (8 min.)\r\n    From the Bibliothèque François Mitterand RER C station, take the CIME train (1 hour)",
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            "id": 509,
            "name": "New session of Molecular Phylogeny - Level 1",
            "shortName": "New session of Phylogénie moléculaire - Niveau 1",
            "description": "OBJECTIF\r\n- Savoir inférer un arbre phylogénétique et l'interpréter\r\n\r\nPRÉREQUIS\r\n- Savoir ce à quoi correspondent des séquences génétiques homologues\r\n- Avoir déjà utilisé les logiciels de base en bioinformatique\r\n- Connaître les notions de base en statistiques (tests, lois probabilistes usuelles, méthodes simples d'estimation de paramètres)\r\n- Avoir des notions de programmation\r\n\r\nPROGRAMME\r\n- Lignes de commandes Linux\r\n- Le format Newick\r\n- Dessin d'arbres\r\n- Alignements multiples et nettoyage\r\n- Modèles d'évolution\r\n- Choix de modèles\r\n- Définitions et propriétés des arbres\r\n- Méthodes de parcimonie\r\n- Méthodes de distance\r\n- Maximum de vraisemblance\r\n- Reconstruction phylogénétique Bayésienne\r\n- Bootstraps et autres supports de branches",
            "homepage": "https://cnrsformation.cnrs.fr/liste-stages-176-Bioinformatique.html",
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                "1200 €"
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                "http://edamontology.org/topic_3293",
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            "updated_at": "2023-10-05T12:37:00.397895Z",
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            "id": 558,
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            "description": "This course offers an introduction to microbial genomics analysis.\r\nIt includes 5 issues: assembly, genome annotation, circos visualization, pan-genome construction, pan-GWAS.",
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                "Genome analysis"
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            "name": "New session of Bioinformatique pour le traitement de données de séquençage (NGS) : analyse de transcriptome",
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            "updated_at": "2023-10-05T12:36:48.888153Z",
            "type": "Training course",
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            "name": "Linux - Initiation / Linux for Beginners - 2022 Session 2",
            "shortName": "Linux Init - 2022 Session 2",
            "description": "Objectifs :\r\n- Être capable de se connecter à une machine Linux\r\n- Être capable de transférer des fichiers à partir de/vers une machine Linux\r\n- Être capable de naviguer dans le système de fichiers\r\n- Être capable d’examiner le contenu d’un fichier et de gérer l’espace disque\r\n- Être capable de gérer les droits d’accès aux répertoires et aux fichiers.\r\n- Être capable de gérer le lancement, l’interruption et l’arrêt de processus",
            "homepage": "http://abims.sb-roscoff.fr/training/courses",
            "is_draft": false,
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            "topics": [
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            "logo_url": "https://abims.sb-roscoff.fr/sites/default/files/abims.png",
            "updated_at": "2023-05-17T09:55:01.623771Z",
            "type": "Training course",
            "start_date": "2022-11-21",
            "end_date": "2022-11-21",
            "venue": "Station Biologique de Roscoff",
            "city": "Roscoff",
            "country": "France",
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            "name": "Short-Read Alignment And Small Size Variants Calling - session 13/11/2023 - 14/11/2023",
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            "description": "This training session, organized jointly with the Sigenae platform, is designed to introduce NGS data, in particular Illumina Solexa technologies with command line. You will discover the new sequence formats, the assembly formats and the known biases of these technologies. You will use mapping on reference genome software, polymorphisms detection with the GATK pipeline and alignment visualization software.\r\n\r\nThis training is focused on the practice. It consists of modules with a large variety of exercises:\r\n\r\nDay 1 (09:00 am to 12:30 am): Fastq format / Sequence quality. Read mapping.\r\nDay 1 (14:00 pm to 17:00 pm): SAM format. Visualisation.\r\nDay 2 (09:00 am to 17:00 am): Variant calling. VCF format. Variant annotation (SNPeff / SNPsift).\r\n \r\nThe session will take place in the room ‘salle de formation’ at INRAE center of Toulouse-Auzeville.\r\n\r\nPrerequisites: ability to use a Unix environment (see Unix training) and Cluster (see Cluster training).\r\n \r\nTool box: FastQC, BWA, Samtools, Picard tools, GATK, SnpSift / SnpEff, IGV.",
            "homepage": "https://bioinfo.genotoul.fr/index.php/events/alignment-and-small-size-variants-calling/",
            "is_draft": false,
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                "Non-academic: 550€ + 20% taxes (TVA)",
                "Academic but non-INRAE: 170 € + 20% taxes (TVA)",
                "For INRAE's staff: 150 € no VAT charged;"
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            "topics": [
                "http://edamontology.org/topic_0102",
                "http://edamontology.org/topic_2885"
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            "updated_at": "2024-06-10T12:36:44.820913Z",
            "type": "Training course",
            "start_date": "2023-11-13",
            "end_date": "2023-11-14",
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            "id": 177,
            "name": "Ecole thématique CNRS Single-cell 2018",
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            "updated_at": "2022-06-02T11:50:50.627601Z",
            "type": "Training course",
            "start_date": "2018-06-17",
            "end_date": "2018-06-22",
            "venue": "Station Biologique",
            "city": "Roscoff",
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            "id": 711,
            "name": "Initiation à Galaxy / Galaxy Initiation",
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            "updated_at": "2025-02-21T08:53:09.273663Z",
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        {
            "id": 706,
            "name": "New session of Formation d'initiation à la plateforme de stockage d'imagerie OMERO",
            "shortName": "New session of Formation d'initiation à OMERO",
            "description": "Cette session d'introduction a pour objectif la prise en main d'OMERO et le chargement d'images vers l'instance OMERO hébergée au Mésocentre Clermont Auvergne, service de la plateforme AuBi.\r\n\r\nQu'est-ce qu'OMERO ?\r\nOMERO est une plateforme logicielle permettant de visualiser, de gérer et d'annoter des données d'images scientifiques. OMERO vous permet d'importer et d'archiver vos images, de les annoter et de baliser vos images, d'enregistrer vos protocoles expérimentaux et d'exporter vos images dans de nombreux formats. Il vous permet également de collaborer avec des collègues en créant des groupes d'utilisateurs.\r\n\r\nPourquoi utiliser OMERO ?\r\nC'est très pratique ! Une fois vos données importées, vous n'avez plus à vous soucier des montages réseau et des structures de dossiers. Vos données sont consultables, vous pouvez les annoter, les visualiser, effectuer des flux de travail simples d'analyse d'images, les partager avec des collaborateurs et générer des figures de niveau publication, le tout directement depuis votre navigateur web.\r\n\r\nComment l'utiliser ?\r\nIl existe deux interfaces principales pour OMERO : un client de bureau (OMERO.insight) et une page web (OMERO.web). Elles ont toutes deux des caractéristiques similaires mais pas identiques. Venez découvrir ces outils lors de cette formation AuBi !\r\n\r\nPour cela, il est indispensable d'être équipé d'un ordinateur portable sur lequel omero insight sera installé en amont de la formation et d'avoir un compte actif au Mésocentre Clermont Auvergne qui vous permettra ensuite de vous connecter sur omero.web.",
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            "type": "Training course",
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            "end_date": "2025-03-12",
            "venue": "",
            "city": "castanet-tolosan",
            "country": "France",
            "geographical_range": "National",
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                    "id": 43,
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            "logo_url": "https://www.france-bioinformatique.fr/wp-content/uploads/logo-ifb-couleur.svg",
            "updated_at": "2023-10-16T08:28:12.972795Z",
            "type": "Training course",
            "start_date": "2023-10-09",
            "end_date": "2023-10-11",
            "venue": "Institut des Systèmes Complexes",
            "city": "Paris",
            "country": "France",
            "geographical_range": "National",
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            "id": 560,
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            "shortName": "",
            "description": "This course offers to develop and enhance advanced Linux shell command line and scripting skills for the processing and analysis of NGS data. We will work on a HPC server and use linux powerful commands to allow to analyze big amount of biological data.",
            "homepage": "https://southgreenplatform.github.io/trainings/linuxJedi/",
            "is_draft": false,
            "costs": [
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            ],
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            "keywords": [],
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                "Linux - Basic Knowledge"
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            "accessConditions": "Open to South Green close collaborators",
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            "logo_url": "https://southgreenplatform.github.io/trainings//images/southgreenlong.png",
            "updated_at": "2023-12-04T15:37:17.765878Z",
            "type": "Training course",
            "start_date": "2023-05-15",
            "end_date": "2023-05-16",
            "venue": "",
            "city": "Montpellier",
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            "homepage": "https://abims.sb-roscoff.fr/training/courses",
            "is_draft": false,
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                "Free"
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                "Basic knowledge of R"
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            "updated_at": "2023-05-17T09:27:31.911754Z",
            "type": "Training course",
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            "country": "France",
            "geographical_range": "",
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            "id": 603,
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            "logo_url": "https://bird.univ-nantes.io/website/images/logo/logo.svg",
            "updated_at": "2024-02-19T09:37:13.928843Z",
            "type": "Training course",
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            "end_date": "2024-03-21",
            "venue": "",
            "city": "Nantes",
            "country": "",
            "geographical_range": "",
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        },
        {
            "id": 538,
            "name": "Workshop nf-core et sarek - 8 et 9 Décembre 2022",
            "shortName": "",
            "description": "Dans le cadre du réseau métier ingénieur.e.s lillois, bilille organise un workshop de 2 jours autour de la communauté internationale et des pipelines de bioinformatique nf-core, les 8 et 9 Décembre sur le campus Cité Scientifique de l’Université de Lille, à Villeneuve d’Ascq.\r\n\r\nLe projet nf-core a été créé en 2018 afin de proposer et maintenir de manière collaborative des pipelines d’analyse de bioinformatique en Nextflow selon des standards stricts de qualité et de reproductibilité, tout en facilitant leur mise en œuvre sur la majorité des infrastructures de calcul. La communauté, très active, qui s’organise autour de cette collection de pipelines rassemble des scientifiques du monde entier, issus de parcours très divers.\r\n\r\nÀ l’occasion de cet atelier, nous accueillerons Maxime Garcia (Seqera labs, Stockholm), membre de l’équipe d’administration nf-core et développeur principal du pipeline d’analyse de variants génomique Sarek. Il présentera la communauté aux participant.e.s et les formera à l’utilisation de ces pipelines d’analyse, en alternant les présentations avec des mises en pratique. Il présentera également les outils de développement mis en place par nf-core pour permettre aux participant.e.s de contribuer aux outils existants et de proposer, si elles et ils le souhaitent, leurs propres pipelines selon les standards de la communauté.",
            "homepage": "https://ums-plbs.univ-lille.fr/workshop-nf-core-et-sarek-avec-maxime-garcia",
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