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            "name": "Annotation and analysis of prokaryotic genomes using the MicroScope platform - novembre 2022",
            "shortName": "MicroScope training - nov 2022",
            "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/",
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                "2500 € for private companies",
                "1350 € for academics",
                "945 € for students"
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                "Licence"
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            "updated_at": "2022-06-02T11:50:50.627601Z",
            "type": "Training course",
            "start_date": "2022-11-21",
            "end_date": "2022-11-25",
            "venue": "Evry University Paris Saclay",
            "city": "Evry",
            "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/",
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            "costs": [
                "Non-academic: 550€ + 20% taxes (TVA)",
                "Academic but non-INRAE: 170 € + 20% taxes (TVA)",
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            "updated_at": "2024-06-10T12:36:44.820913Z",
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            "start_date": "2023-11-13",
            "end_date": "2023-11-14",
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            "name": "LINUX - session 07/10/2024",
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            "description": "This training session is organized by the Genotoul bioinfo platform and aims at learning sequence analysis. This training session has been designed to familiarize yourself with the platform resources and its organization. You will learn to access the platform from your work station, what is an Linux environment and how to use it, how to create and manipulate files, how to transfer them from and to your personal computer.\r\n\r\nThis training is focused on practice. It consists of 3 modules with a large variety of exercises:\r\n\r\n- Connect to « genotoul » server (09:00 am to 10:30 am): Platform presentation, Linux basics, opening an user account, Putty installation, first connection.\r\n- Files and basics commands  (10:45 am to 12:00 pm): types of files and secure access, file manipulation commands, text editors and viewers, disk space management .\r\n- Transfers and file manipulation (14:00 pm to 17:00 pm): download/transfer, compress/uncompress, utility commands and data extraction, output redirections.",
            "homepage": "http://bioinfo.genotoul.fr/index.php/events/linux-2-2/",
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                "Non-academic: 550€ + 20% taxes (TVA)",
                "Academic but non-INRAE: 170 € + 20% taxes (TVA)",
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            "updated_at": "2024-06-05T09:15:55.325587Z",
            "type": "Training course",
            "start_date": "2024-10-07",
            "end_date": "2024-10-07",
            "venue": "",
            "city": "castanet-tolosan",
            "country": "France",
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                    "id": 137,
                    "name": "Linux slides - Genotoul-bioinfo",
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                    "id": 138,
                    "name": "Linux TP - Genotoul-bioinfo",
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            "id": 669,
            "name": "Using sed and awk to modify large large text files - 13 March 2025",
            "shortName": "",
            "description": "Many analysis generate large result text files which have to be checked, merged, split, reduced. Several tools have been developed and are available on Unix to do this, including sed and AWK. During this course you will be trained to process large files with sed and AWK. Sed is tool enabling to select and process lines. You can easily insert, delete, modify, append lines to very large files with millions of lines. AWK will enable to perform more fine tuned file modifications based on columns. It includes also more mathematical and string functions.  The course is based mainly on exercises with small sections presenting concepts and commands.",
            "homepage": "http://bioinfo.genotoul.fr/index.php/events/modify-and-extract-information-from-large-text-files-day-2-3/",
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                "Non-academic: 550€ + 20% taxes (TVA)",
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            "updated_at": "2024-12-06T20:47:41.482360Z",
            "type": "Training course",
            "start_date": "2025-03-13",
            "end_date": "2025-03-13",
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            "id": 746,
            "name": "RNASeq Analysis",
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            "homepage": "https://pf-bird.univ-nantes.fr/training/rnaseq/",
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            "logo_url": "https://bird.univ-nantes.io/website/images/logo/logo.svg",
            "updated_at": "2026-01-27T10:34:29.823975Z",
            "type": "Training course",
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            "end_date": "2025-11-04",
            "venue": "",
            "city": "Nantes",
            "country": "",
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            "logo_url": "https://bird.univ-nantes.io/website/images/logo/logo.svg",
            "updated_at": "2024-08-22T15:55:32.866676Z",
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            "venue": "",
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            "name": "Introduction To Python - session 16/10/2024 - 17/10/2024",
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            "description": "The Toulouse Genotoul bioinformatics platform, organizes a 2 days long training course for non computer scientist and biologists aiming at learning the foundation of Python programming. In this training you will learn the basics of programming (variables, functions, control structures such as “if” condition, “for” loop”), writing simple programs which read files, and write results to others. The training course does not require any knowledge in programming, but basic Linux/bash commands are required (cd, ls).\r\n\r\nThis training focuses on practice. It consists of modules with a large variety of exercises described hereunder (PROVISIONAL SCHEDULE):\r\n\r\nUsing a Jupyter notebook (Day 1).\r\nUsing variables (Day 1).\r\nBasic operations and functions (Day 1).\r\nReading a file, writing to a file (Day 1).\r\nCharacter string manipulation (Day 1).\r\nLists and dictionaries (Day 2).\r\nThe if and for controls (Day 2).\r\nBases of algorithms (Day 2).",
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            "updated_at": "2024-06-10T12:33:57.629350Z",
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            "end_date": "2024-10-17",
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            "id": 601,
            "name": "Introduction to Linux",
            "shortName": "Introduction to Linux - BiRD",
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            "homepage": "https://pf-bird.univ-nantes.fr/training/",
            "is_draft": false,
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            "logo_url": "https://bird.univ-nantes.io/website/images/logo/logo.svg",
            "updated_at": "2024-02-19T09:37:34.209594Z",
            "type": "Training course",
            "start_date": "2024-03-18",
            "end_date": "2024-03-18",
            "venue": "Faculté de Pharmacie - Salle 450, 4ème étage",
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        {
            "id": 511,
            "name": "New session of Molecular Phylogeny - Level 2",
            "shortName": "New session of Phylogénie moléculaire - Niveau 2",
            "description": "OBJECTIF\r\n- Être capable de tester des hypothèses et d'ajuster des modèles permettant de comprendre l'évolution à l'échelle moléculaire\r\n\r\nPRÉREQUIS\r\n- Avoir déjà utilisé les logiciels de base en phylogénie moléculaire\r\n- Maîtriser les notions de base en statistiques (tests statistiques, principe du bootstrap, intervalles de confiances, etc.) et de probabilités (probabilités jointes / conditionnelles, théorème de Bayes, etc.)\r\n- Maîtriser un langage de programmation\r\n- Notions de phylogénie moléculaire\r\nAvoir suivi le stage \"Phylogénie moléculaire - formation de base\" ou niveau équivalent \r\n\r\nPROGRAMME\r\n- Phylogénétique et génétique des populations\r\n- Détection de sélection positive au sein de séquences codantes\r\n- Datation moléculaire : intégrer fossiles et molécules\r\n- Phylogénomique\r\n- Super-arbres et super-matrices, réconciliations d'arbres\r\n- Visualisation de l'information en phylogénie\r\n- Placement phylogénétique\r\n- Bases d'épidémiologie (modèles en compartiments, ODE, applications, etc)\r\n- Simulations selon une variété de modèles épidémiologiques\r\n- Phylodynamique : combiner épidémiologie et évolution",
            "homepage": "https://cnrsformation.cnrs.fr/liste-stages-176-Bioinformatique.html",
            "is_draft": false,
            "costs": [
                "Priced",
                "1200 €"
            ],
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            "keywords": [
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                "Selection Detection",
                "Phylogenomics"
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            "accessConditions": "",
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            "logo_url": "http://www.atgc-montpellier.fr/pictures/ATGClogo.svg",
            "updated_at": "2023-10-05T12:36:32.255069Z",
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            "end_date": "2023-10-06",
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            "id": 670,
            "name": "Analysis of shotgun metagenomic data - May 2025",
            "shortName": "",
            "description": "This training session is organized by the Genotoul bioinfo platform. This course is dedicated to the analysis of prokaryotic shotgun metagenomic data from Illumina and Pacbio HiFi sequencing technology. \r\n\r\nAfter an overview of metagenomics and the biases and limitations of analyses, we will look at the main steps involved in analysing metagenomic data and launch independent tools on the genobioinfo cluster.\r\nLearners will then test a workflow to automate processing on a test dataset (metagWGS ).\r\nOn the third day, learners will choose which analysis strategy to start with according to their experimental design and launch the first stage of metagWGS on their own data.\r\nBy the end of the course, trainees will be familiar with the scope, advantages and limitations of shotgun sequencing data analysis and will have started the analysis on their own data.\r\n\r\ncalendar\r\n \r\n\r\nThis training is focused on practice. It consists of several modules with a large variety of exercises:\r\n\r\nFirst Day\r\nStart at 09:00 am\r\nTour de table\r\nIntroduction to metagenomics, Illumina and Pacbio data, analysis stages, analysis limits, etc.\r\nPresentation of some key tools for each stage\r\nPractical work on the main stages launched independently\r\nEnd at 17:00 pm\r\nSecond Day\r\nStart at 09:00 am\r\nIntroduction to the advantages and disadvantages of workflows and containers\r\nLaunch of the data cleansing stage\r\nLaunch of the rest of the workflow and analysis of the multiQC report\r\nEnd at 17:00 pm\r\nThird Day – BYOD\r\nStart at 09:00 am\r\nDefine the analysis strategy and launch the start of the analysis of your own data.\r\nEnd at 17:00 pm maximum",
            "homepage": "https://bioinfo.genotoul.fr/index.php/events/analysis-of-shotgun-metagenomic-data/",
            "is_draft": false,
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                "Academic non-INRAE for academic but non-INRAE: 510 € + 20% taxes (TVA)",
                "INRAE for INRAE's staff: 450 € no VAT charged"
            ],
            "topics": [
                "http://edamontology.org/topic_3174"
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                "Metagenomics"
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                {
                    "id": 88,
                    "name": "BioinfOmics",
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            ],
            "logo_url": "http://bioinfo.genotoul.fr/wp-content/uploads/bioinfo_logo-rvb-petit.png",
            "updated_at": "2024-12-06T20:59:00.699915Z",
            "type": "Training course",
            "start_date": "2025-05-05",
            "end_date": "2025-05-07",
            "venue": "",
            "city": "castanet-tolosan",
            "country": "France",
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            "registration_opening": "2024-12-06",
            "registration_closing": "2025-04-23",
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        },
        {
            "id": 589,
            "name": "NGS data analysis on the command line - Session 6",
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            "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": [
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            ],
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            ],
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            ],
            "logo_url": null,
            "updated_at": "2024-01-22T14:58:13.640466Z",
            "type": "Training course",
            "start_date": "2024-03-11",
            "end_date": "2024-03-15",
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            "city": "Strasbourg",
            "country": "",
            "geographical_range": "Local",
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            ],
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        },
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            "name": "Analyses Single Cell RNA-seq (ScRNA-seq) avec R",
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            "homepage": "https://cnrsformation.cnrs.fr/analyses-single-cell-rna-seq-scrna-seq-avec-r?axe=176",
            "is_draft": false,
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            "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": [
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            ],
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                {
                    "id": 6,
                    "name": "CNRS formation entreprise",
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            ],
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            ],
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                {
                    "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": "2025-12-09T10:09:10.250876Z",
            "type": "Training course",
            "start_date": "2026-06-11",
            "end_date": "2026-06-12",
            "venue": "",
            "city": "Bordeaux",
            "country": "France",
            "geographical_range": "National",
            "trainers": [
                "https://catalogue.france-bioinformatique.fr/api/userprofile/34/?format=api",
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            "trainingMaterials": [],
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            "realisation_status": "future",
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            "registration_closing": "2026-06-01",
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        },
        {
            "id": 503,
            "name": "NGS data analysis on the command line - session 4",
            "shortName": "NGS-analysis-cli - session4",
            "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://gitlab.com/ngs_workshop/april2022",
            "is_draft": false,
            "costs": [
                "Free to academics"
            ],
            "topics": [
                "http://edamontology.org/topic_0102",
                "http://edamontology.org/topic_2269",
                "http://edamontology.org/topic_3170",
                "http://edamontology.org/topic_3168"
            ],
            "keywords": [],
            "prerequisites": [
                "none"
            ],
            "openTo": "Internal personnel",
            "accessConditions": "This training is dedicated to academics working in a laboratory of Unistra/CNRS.",
            "maxParticipants": 12,
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            ],
            "organisedByTeams": [
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            ],
            "logo_url": null,
            "updated_at": "2022-11-28T14:04:22.544121Z",
            "type": "Training course",
            "start_date": "2022-03-31",
            "end_date": "2022-04-04",
            "venue": "",
            "city": "Strasbourg",
            "country": "France",
            "geographical_range": "",
            "trainers": [],
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            "registration_opening": null,
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        },
        {
            "id": 634,
            "name": "Short-Read Alignment And Small Size Variants Calling - session 9/10/2024 - 10/10/2024",
            "shortName": "",
            "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,
            "costs": [
                "Non-academic: 550€ + 20% taxes (TVA)",
                "Academic but non-INRAE: 170 € + 20% taxes (TVA)",
                "For INRAE's staff: 150 € no VAT charged;"
            ],
            "topics": [
                "http://edamontology.org/topic_0102",
                "http://edamontology.org/topic_2885"
            ],
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                    "name": "Genotoul-bioinfo",
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            ],
            "logo_url": "https://bioinfo.genotoul.fr/wp-content/uploads/sigenae-text-black-1.png",
            "updated_at": "2024-06-10T12:36:32.603065Z",
            "type": "Training course",
            "start_date": "2024-10-09",
            "end_date": "2024-10-10",
            "venue": "",
            "city": "castanet-tolosan",
            "country": "France",
            "geographical_range": "",
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            ],
            "trainingMaterials": [],
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            "realisation_status": "past",
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        },
        {
            "id": 722,
            "name": "HOW TO RUN A NF-CORE NEXTFLOW WORKFLOW ON GENOTOUL ? December 1er 2025",
            "shortName": "Nextflow/nf-core",
            "description": "This training session is organized by the Genotoul bioinfo platform and aims at learning nf-core workflow submission, error understanding, resuming jobs and ressource reservation. We will present and practice:\r\n\r\nthe Nextflow software\r\nthe nf-core community and pipelines\r\nWhat is a singularity image ?\r\nWhere are installed the nf-core workflows ? Which version do I use ?\r\nHow to run a workflow and which config file is used ?\r\nWhich kind of error I can get ?\r\nHow to resume failed jobs?\r\nHow to handle genome indexes ?\r\nHow to monitor my process and then well configure my workflow ?\r\nHow do you best adjust CPU and RAM reservations?\r\nThis is NOT a bioinformatic training on a particular workflow or a training on how to develop a workflow.\r\n\r\nThis training is focused on practice. It consists of several modules with a large variety of exercises:\r\n\r\nStart at 09:00 am\r\nEnd at 17:00 pm",
            "homepage": "https://bioinfo.genotoul.fr/index.php/events/how-to-run-a-nf-core-nextflow-workflow-on-genotoul-2/",
            "is_draft": false,
            "costs": [
                "Non-academic: 550€ + 20% taxes (TVA)",
                "Academic but non-INRAE: 170 € + 20% taxes (TVA)",
                "For INRAE's staff: 150 € no VAT charged;"
            ],
            "topics": [
                "http://edamontology.org/topic_0769"
            ],
            "keywords": [
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            ],
            "prerequisites": [
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                "Cluster"
            ],
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            ],
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                    "id": 22,
                    "name": "Genotoul-bioinfo",
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            ],
            "logo_url": "http://bioinfo.genotoul.fr/wp-content/uploads/bioinfo_logo-rvb-petit.png",
            "updated_at": "2025-05-09T13:20:57.741969Z",
            "type": "Training course",
            "start_date": "2025-12-01",
            "end_date": "2025-12-01",
            "venue": "",
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            "country": "France",
            "geographical_range": "",
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            ],
            "computingFacilities": [],
            "realisation_status": "past",
            "registration_opening": "2025-05-09",
            "registration_closing": "2025-11-24",
            "registration_status": "closed",
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        },
        {
            "id": 745,
            "name": "Annotation and analysis of prokaryotic genomes using the MicroScope platform",
            "shortName": "MicroScope training - April 2026",
            "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": [
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