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                    "id": 19,
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            "updated_at": "2024-12-11T08:35:40.374521Z",
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            "costs": [
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            "keywords": [
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            "updated_at": "2025-01-29T11:32:53.505947Z",
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            "start_date": "2025-05-19",
            "end_date": "2025-05-20",
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            "city": "Jouy-en-Josas",
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        },
        {
            "id": 524,
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            "shortName": "Git Initiation 2023 S1",
            "description": "Objectifs\r\n- Savoir définir ce qu’est un outil de gestion de version\r\n- Être capable d’initialiser un entrepôt Git pour un projet\r\n- Être capable de définir quels fichiers inclure/exclure d’un projet\r\n- Savoir enregistrer localement une nouvelle version pour un projet\r\n- Savoir partager des modifications locales avec tous les contributeurs d’un projet\r\n- Savoir gérer des modifications en parallèle en utilisant les branches.\r\n- Connaître les bonnes pratiques pour contribuer à projet tiers\r\nProgramme :\r\n- Présentation des avantages de la gestion de versions (projets individuels & projets collaboratifs)\r\n- Présentation des principes de fonctionnement de Git\r\n- Présentation et mise en œuvre des commandes principales de Git (clone, checkout, add, rm, commit, merge,\r\npush, pull) ; en ligne de commande ou en utilisant une interface graphique (GitHub et GitLab)",
            "homepage": "https://abims.sb-roscoff.fr/training/courses",
            "is_draft": false,
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            ],
            "logo_url": "https://abims.sb-roscoff.fr/sites/default/files/abims.png",
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            "type": "Training course",
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            "end_date": "2023-06-23",
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            "city": "Roscoff",
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        {
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            "description": "The Toulouse Genotoul bioinformatics platform, in collaboration with the Genotoul Biostatistics platform, and the MIAT unit, organize a 3,5 days long training course for bio-informaticians and biologists aiming at learning sequence analysis. It focuses on (protein coding) gene expression analysis using reads produced by ‘RNA-Seq’. This training session is designed to introduce sequences from ‘NGS’ (Next Generation Sequencing), particularly Illumina platforms (HiSeq). You will discover the standards file formats, learn about the usual biases of this type of data and run different kinds of analyses, such as spliced alignment on a reference genome, novel gene and transcript discovery, expression quantification of coding genes and transcripts. Finally you will be able to extract the differentially expressed genes.",
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