Handles creating, reading and updating training events.

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            "name": "Analysis of shotgun metagenomic data",
            "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",
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                "http://edamontology.org/topic_3174"
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            "id": 412,
            "name": "Construction and analysis of eukaryotic pangenome graphs",
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            "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.",
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            "name": "LINUX",
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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": "https://bioinfo.genotoul.fr/index.php/events/linux-2-2/",
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                "http://edamontology.org/topic_3316"
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            "logo_url": "https://bioinfo.genotoul.fr/wp-content/uploads/bioinfo_logo-rvb-petit.png",
            "updated_at": "2025-12-09T09:42:16.231660Z",
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            "id": 332,
            "name": "SHORT-READ ALIGNMENT AND SMALL SIZE VARIANTS CALLING",
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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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                "Non-academic: 550€ + 20% taxes (TVA)",
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            "logo_url": "https://bioinfo.genotoul.fr/wp-content/uploads/sigenae-text-black-1.png",
            "updated_at": "2025-12-01T11:54:41.351028Z",
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            "id": 409,
            "name": "Introduction to single-cell RNAseq analysis",
            "shortName": "Intro Single-cell",
            "description": "Objectives\r\n- Understand and learn the main steps of scRNA-seq data analysis, up to marker gene detection and cell type identification.\r\n- Be able to use the Seurat package on a small test dataset, from count matrices to clustering and cluster annotation.\r\n- Understand the basics of the analysis in order to apply them to one’s own dataset.\r\n\r\nCourse Content\r\nI. Introduction\r\n- Single-cell RNA sequencing\r\n- From raw sequencing data to count matrices\r\n- Software tools\r\n\r\nII. Preprocessing of the expression matrix (Theory and Practice)\r\n- Quality control\r\n- Normalization\r\n- Dimensionality reduction (HVG, PCA, UMAP)\r\n- Detection of expression biases\r\n\r\nIII. Annotation (Theory and Practice)\r\n- Clustering\r\n- Marker genes\r\n- Cell type identification\r\n- Analysis of marker gene lists with the R package ClusterProfiler\r\n\r\nIV. Practical Workshop “Bring your own data”\r\n- Semi-autonomous execution of primary analysis on learners’ own data",
            "homepage": "https://pf-bird.univ-nantes.fr/training/singlecell/",
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            "updated_at": "2026-03-26T14:34:54.143222Z",
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            "id": 407,
            "name": "Optimal use of GLiCID HPC cluster",
            "shortName": "GLiCID",
            "description": "Objectives\r\n- understand the infrastructure of GLiCID HPC cluster\r\n- understand the different types of storage and computing nodes\r\n- launch computing tasks via the Slurm scheduler\r\n\r\nCourse Content\r\n- configuration of your account and connection with ssh on GLiCID (ssh keys)\r\n- navigate through the storage spaces\r\n- use slurm to launch a job\r\n- manage the software environments (micromamba, guix, modules)\r\n- use workflow managers on GLiCID",
            "homepage": "https://pf-bird.univ-nantes.fr/training/cluster/",
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            "id": 288,
            "name": "Introduction to the command-line interface",
            "shortName": "BirdLinux",
            "description": "Objectives\r\n- Understand the principles and advantages of the Linux system\r\n- Know and use the main bash commands.\r\n- Ability to chain multiple commands using pipes\r\n- Launch programs with arguments\r\n- Gain independence to perform command line analyses\r\n\r\nCourse Content\r\n- Introduction to the Linux system.\r\n- File system: directory structure, paths, home directory, file and directory management.\r\n- Principle of protections: reading file attributes, access rights, management of user groups.\r\n- Useful commands for file manipulation\r\n- Redirection operators (command input/output)\r\n- Creating and running a bash script\r\nIntroduction to environment variables\r\nConnecting to a remote server via a terminal or via WSL",
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            "name": "Introduction to R",
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            "description": "Objectives\r\n- Understand basic R commands\r\n- Learn how to use the RStudio interface\r\n- Understand the use of R functions\r\n- Be able to perform simple data manipulations\r\n- Be able to create basic visualizations\r\n\r\nCourse Content\r\nI. Introduction\r\n- Getting started with the RStudio environment\r\n- Programming best practices\r\n- Different types and classes of variables\r\n- Functions\r\n\r\nII. Data manipulation with the tidyverse\r\n- Logical operators\r\n- Working with data frames\r\n\r\nIII. Visualization with ggplot2\r\n- Principles\r\n- Simple examples",
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