Handles creating, reading and updating events.

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            "description": "Bilille propose chaque année un cycle de formation d'introduction à l'analyse des données de séquençage à haut débit.\r\nCe cycle est composé de 6 modules, à la carte : \r\n- Module 1: Analyses ADN\r\n- Module 2: Analyses de variants\r\n- Module 3 : Métagénomique\r\n- Module 4: ChIP-seq\r\n- Module 5: Analyses RNA-seq, bioinformatique\r\n- Module 6: Analyses RNA-seq, biostatistique\r\nLes fiches descriptives sont accessibles sur le site de Bilille. Chaque module comprend des présentations générales et des séances pratiques sur ordinateur, avec Galaxy.\r\nLes objectifs du module 5 sont :\r\n- Savoir réaliser une analyse transcriptomique par RNA-seq avec ou sans (de novo) génome de référence à l’aide du portail Galaxy\r\n- Avoir un regard critique sur la qualité des lectures obtenues par le séquenceur\r\n- Connaître et savoir paramétrer les outils nécessaires à l’analyse",
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            "description": "Ce cours théorique et pratique de deux semaines est orienté sur les méthodes pour étudier la synthèse, maturation et la dégradation d’une large variété de molécules d’ARN dans les cellules eucaryotes - voir plus\n",
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            "name": "5th workshop Single-Cell : Transcriptomics, Spatial and Long reads",
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            "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.\r\n\r\nAll the classes will be taught in English",
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            "venue": "Station Biologique",
            "city": "Roscoff",
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            "name": "Linux Avancé / Advanced Linux - 2022 Session2",
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            "description": "Objectifs\r\n- Savoir utiliser des commandes linux pour traiter de grosses quantités de données : fichiers\r\nvolumineux et/ou en grands nombres : recherche, comptage, tri, fusion, …\r\nProgramme\r\n- Introduction\r\n- Décrire (wc, grep)\r\n- Manipuler des fichiers tabulés (cut, sort)\r\n- Rechercher (grep)\r\n- Redirection / Pipeline (stdin, stdout, stderr, >, 2>, &&, |)\r\n- Recherche avancée : notion d’expression régulière (egrep)\r\n- Rechercher/Remplacer haut débit (tr, sed)\r\n- Manipulation de fichier tabulé – mode avancé (awk)\r\n- Traitement séquentiel de nombreux fichiers (for)",
            "homepage": "https://abims.sb-roscoff.fr/training/courses",
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                    "name": "SBR - Roscoff Marine Station",
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            "logo_url": "https://abims.sb-roscoff.fr/sites/default/files/abims.png",
            "updated_at": "2023-05-17T09:55:24.793130Z",
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            "name": "Introduction to High-performance computing",
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            "description": "This course offers an introduction on how to work with HPC Southgreen clusters. It is intended for new users, with the goals of improving user productivity and minimizing the obstacles. The HPC Southgreen cluster are presented, together with the tools to be able to use it. Module load notion, interactive usage and batch jobs submittions will be developped.\nPrerequisites\nLinux Basics\n\nProgram\nIntroduction to HPCs architecture\nDiscover Sun grid Engine (SGE)\nData Management on clusters\nInteractive Usage\nSubmit batch jobs\n\n\nLearning objectives\nAfter this course, participants should be able to:\nUse the HPC resources interactively\nManage data copies\nUse module load\nsubmit batch jobs\n\n\nInstructors\n\n\nNdomassi Tando (NT) - ndomassi.tando@ird.fr\nBertrand Pitollat(BP) - bertrand.pitollat@cirad.fr\nAlexis Dereeper (AD) - alexis.dereeper@ird.fr​\n\n",
            "homepage": "https://southgreenplatform.github.io/trainings//HPC/",
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            "updated_at": "2022-06-02T11:50:50.627601Z",
            "type": "Training course",
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            "city": "Centre IRD, Montpellier",
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            "id": 264,
            "name": "Bioinformatique pour le traitement de données de séquençage (NGS)",
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            "description": "\nLes objectifs sont :\n- Savoir choisir les outils d'analyse\n- Etre autonome pour effectuer un pipeline d'analyse\n- Comprendre les principes des méthodes d'analyse\n- Savoir manipuler les fichiers de séquences : préparation et filtration\n- Etre capable d'évaluer la qualité des données\n- Savoir analyser avec ou sans génome de référence\nhttps://cnrsformation.cnrs.fr/\n\n",
            "homepage": "http://cnrsformation.cnrs.fr/stage-17010-Bioinformatique-pour-le-traitement-de-d…",
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                "NGS Data Analysis",
                "Analysis of RNAseq data",
                "Assembly of genomes and transcriptomes",
                "Read alignment on genomes",
                "Variant analysis",
                "Complete genomes",
                "Transcriptomics (RNA-seq)",
                "Genomics (DNA-seq)",
                "NGS Sequencing Data Analysis"
            ],
            "prerequisites": [],
            "openTo": "Internal personnel",
            "accessConditions": "S'acquitter des frais d'inscription, notions de base en informatique : fichiers, répertoire..., notions du système linux et des lignes de commandes, niveau master\n",
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            "updated_at": "2022-06-02T11:50:50.627601Z",
            "type": "Training course",
            "start_date": "2019-03-24",
            "end_date": "2019-03-28",
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        },
        {
            "id": 270,
            "name": "Biotechnologies et bioinformatique appliquées aux maladies rares",
            "shortName": "",
            "description": "Module optionnel du DIU Maladies rares : de la recherche au traitement.\n",
            "homepage": "http://fondation-maladiesrares.org/actualite/diu-maladies-rares-de-la-recherche-…",
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                "Bioinformatics & Biomedical",
                "Sequence analysis",
                "NGS Sequencing Data Analysis"
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                "Autre (Diplôme universitaire, école d'ingénieur ...)"
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            "accessConditions": "Inscription au DIU Maladies rares : de la recherche au traitement\n",
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            "updated_at": "2022-06-02T11:50:50.627601Z",
            "type": "Training course",
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            "end_date": "2017-02-09",
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            "id": 756,
            "name": "SHORT-READ ALIGNMENT AND SMALL SIZE VARIANTS CALLING - 13 avril 2026",
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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.",
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            "is_draft": false,
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