Training List
Handles creating, reading and updating training events.
GET /api/training/?format=api&offset=320&ordering=-openTo
{ "count": 391, "next": "https://catalogue.france-bioinformatique.fr/api/training/?format=api&limit=20&offset=340&ordering=-openTo", "previous": "https://catalogue.france-bioinformatique.fr/api/training/?format=api&limit=20&offset=300&ordering=-openTo", "results": [ { "id": 378, "name": "Les langages de workflows pour une analyse bioinformatique reproductible / Workflow languages for reproducible bioinformatics analysis", "shortName": "WF4bioinfo", "description": "L’Institut Français de Bioinformatique (IFB) organise en partenariat avec iPOP-UP (représenté par EDC) une formation sur les langages de workflows en bioinformatique à destination des bioinformaticien·ne·s et des bioanalystes. La formation abordera les fondamentaux et les fonctionnalités avancées des deux langages Snakemake et Nextflow. Ces outils sont en effet devenus indispensables pour assurer la reproductibilité et l’efficacité des analyses bioinformatiques. La formation sera structurée en deux séquences :\r\n- une journée commune qui abordera les grands principes des gestionnaires de workflow, en particulier dans le domaine de la bioinformatique et en lien avec les infrastructures de calcul de type cluster et cloud proposés au sein de l’IFB \r\n- une journée de session pratique avec 1 atelier snakemake et 1 atelier nextflow en parallèle au choix des participants. Nous proposons aux participants qui le souhaitent de travailler sur leur propre workflow dans une approche “Bring your own script” avec l’aide de l’équipe pédagogique.", "homepage": "https://moodle.france-bioinformatique.fr/course/view.php?id=29", "is_draft": false, "costs": [], "topics": [ "http://edamontology.org/topic_0769", "http://edamontology.org/topic_0091" ], "keywords": [ "FAIR", "Reproducibility", "Nextflow", "Snakemake" ], "prerequisites": [ "Linux - Basic Knowledge" ], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 20, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/116/?format=api", "https://catalogue.france-bioinformatique.fr/api/userprofile/326/?format=api", "https://catalogue.france-bioinformatique.fr/api/userprofile/804/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 4, "name": "IFB - ELIXIR-FR", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/IFB%20-%20ELIXIR-FR/?format=api" } ], "organisedByTeams": [ { "id": 38, "name": "PB-IBENS", "url": "https://catalogue.france-bioinformatique.fr/api/team/PB-IBENS/?format=api" } ], "logo_url": "https://moodle.france-bioinformatique.fr/pluginfile.php/1/core_admin/logocompact/300x300/1654772049/IFB-HAUT-COULEUR-PETIT.png", "updated_at": "2024-03-26T16:42:31.487108Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "Intermediate", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/613/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/664/?format=api" ] }, { "id": 314, "name": "Workflow4metabolomics", "shortName": "W4E", "description": "Processing, statistical analysis, and annotation of metabolomics data is a complex task for experimenters since it involves many steps and requires a good knowledge of both the methodology and software tools. The Workflow4Metabolomics.org (W4M) online infrastructure provides a user-friendly and high-performance environment with advanced computational modules for building, running, and sharing complete workflows for LC-MS, GC-MS, FIA and NMR analysis. Such features are of major values for teaching computational metabolomics to experimenters, and previous courses using W4M since 2014 have been very successful.", "homepage": "https://workflow4metabolomics.org/", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 20, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": null, "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/472/?format=api" ] }, { "id": 271, "name": "Bioinformatique pour le traitement de données de séquençage (NGS) : analyse de transcriptome", "shortName": "", "description": "OBJECTIFS\r\n- Comprendre les principes des méthodes d'analyse de données de séquençage à haut débit\r\n- Comprendre les résultats obtenus, les paramètres et leurs impacts sur les analyses\r\n- Savoir choisir et utiliser les principaux outils d'analyse\r\n- Être autonome pour utiliser un pipeline d'analyse\r\n- Savoir manipuler les fichiers de séquences : préparation et filtration\r\n- Savoir évaluer la qualité des données\r\n- Savoir analyser les résultats avec ou sans génome de référence\r\n\r\nPRÉREQUIS\r\n- Notions de base en informatique : fichiers, répertoire...\r\n- Notions du système linux et des lignes de commande\r\n- Niveau master \r\n\r\nPROGRAMME\r\n- Linux : commandes de base\r\n- Les données NGS : fichiers, manipulation de base, nettoyage\r\n- Mapping : principaux outils et pratique\r\n- Transcriptomique :\r\n. analyse de RNA-seq : expression différentielle des gènes / des ARNs (comptage et DESeq2) ; comparaison d'échantillons issus de conditions différentes\r\n. post-analyse : analyse GO, interrogation bases de connaissances (ex : KEGG), création de graphique (en R)\r\n. analyse couplée transcriptome / traductome", "homepage": "", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [ "NGS Sequencing Data Analysis" ], "prerequisites": [], "openTo": "Everyone", "accessConditions": "PUBLICS :\r\n- Biologistes, professionnels des sciences du vivant ayant besoin d'analyser des données de séquençage\r\n- Ingénieurs ou chercheurs en bioinformatique\r\n- Bioanalystes\r\n \r\nPRÉREQUIS\r\n- Notions de base en informatique : fichiers, répertoire...\r\n- Notions du système linux et des lignes de commande\r\n- Niveau master", "maxParticipants": 12, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/528/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 1, "name": "CNRS formation entreprises", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/CNRS%20formation%20entreprises/?format=api" } ], "organisedByTeams": [ { "id": 7, "name": "ATGC", "url": "https://catalogue.france-bioinformatique.fr/api/team/ATGC/?format=api" } ], "logo_url": "https://ressources.france-bioinformatique.fr/sites/default/files/ATGClogox120.png", "updated_at": "2023-01-24T10:47:30.457628Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/401/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/510/?format=api" ] }, { "id": 332, "name": "SHORT-READ ALIGNMENT AND SMALL SIZE VARIANTS CALLING", "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_2885", "http://edamontology.org/topic_0102" ], "keywords": [], "prerequisites": [ "Linux/Unix", "Cluster" ], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 12, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 37, "name": "MIAT - Mathématiques et Informatique Appliquées de Toulouse", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/MIAT%20-%20Math%C3%A9matiques%20et%20Informatique%20Appliqu%C3%A9es%20de%20Toulouse/?format=api" } ], "organisedByTeams": [ { "id": 22, "name": "Genotoul-bioinfo", "url": "https://catalogue.france-bioinformatique.fr/api/team/Genotoul-bioinfo/?format=api" } ], "logo_url": "https://bioinfo.genotoul.fr/wp-content/uploads/sigenae-text-black-1.png", "updated_at": "2025-12-01T11:54:41.351028Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/756/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/634/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/530/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/724/?format=api" ] }, { "id": 301, "name": "MIAPPE, Minimum Information About Plant Phenotyping Experiments", "shortName": "MIAPPE", "description": "The Minimal Information About Plant Phenotyping Experiments (MIAPPE, www.miappe.org) standard has been designed by ELIXIR, EMPHASIS and Bioversity international to guide plant scientist in the management of experimental data. Furthermore, since genetic studies relies on the integration and the linking between phenotype and genotype datasets, relevant section of MIAPPE are beginning to be used for genotyping standards.\r\nThis formation will cover a general introduction of the MIAPPE principles and some examples to illustrate different use cases on the usage of MIAPPE for plant phenotyping data standardization.", "homepage": "", "is_draft": false, "costs": [ "Free" ], "topics": [ "http://edamontology.org/topic_3298", "http://edamontology.org/topic_3572", "http://edamontology.org/topic_0219", "http://edamontology.org/topic_0625", "http://edamontology.org/topic_0780" ], "keywords": [ "Données" ], "prerequisites": [ "none" ], "openTo": "Everyone", "accessConditions": "Public", "maxParticipants": null, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/504/?format=api", "https://catalogue.france-bioinformatique.fr/api/userprofile/441/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 39, "name": "URGI - US1164", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/URGI%20-%20US1164/?format=api" }, { "id": 82, "name": "INRAE", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INRAE/?format=api" } ], "organisedByTeams": [ { "id": 26, "name": "URGI", "url": "https://catalogue.france-bioinformatique.fr/api/team/URGI/?format=api" } ], "logo_url": "https://urgi.versailles.inra.fr/extension/inra/design/urgi/images/logoURGI_res72_2-82X1-98.png", "updated_at": "2025-11-28T13:19:07.566534Z", "audienceTypes": [ "Graduate", "Professional (initial)", "Professional (continued)" ], "audienceRoles": [ "All" ], "difficultyLevel": "Novice", "trainingMaterials": [ { "id": 150, "name": "Plant Data Managment for Phenotyping Experiments - MIAPPE", "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/Plant%20Data%20Managment%20for%20Phenotyping%20Experiments%20-%20MIAPPE/?format=api" } ], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": false, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/732/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/733/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/734/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/736/?format=api" ] }, { "id": 405, "name": "Annotation et comparaison de génomes bactériens", "shortName": "Annotation et comparaison de génomes bactériens", "description": "Connaître les concepts et les principales méthodes bioinformatiques pour annoter automatiquement et comparer un jeu de données de génomes bactériens. Construire et évaluer la qualité d’un jeu de données publiques. Évaluer la qualité et annoter automatiquement un jeu de données. Savoir mettre en oeuvre une comparaison de génomes et en interpréter les résultats.\r\n\r\nProgramme :\r\n\r\n* Construction d’un jeu de données :\r\n Téléchargement de données publiques\r\n Evaluation de la qualité d’un jeu de données\r\n\r\n* Principes et mise en œuvre d’une annotation automatique d’un génome bactérien\r\n\r\n * Caractérisation de la diversité génomique\r\n\r\n * Construction de pangénomes\r\n\r\n * Analyse des résultats :\r\n Résultats et métriques d’un pangénome\r\n Notions élémentaires de phylogénomique\r\n Visualisation et interprétation des résultats\r\n\r\n * Mise en pratique sur un jeu de données bactériens, utilisation des logiciels dRep, Quast, Bakta et PPanGGOLiN sous Galaxy.", "homepage": "https://documents.migale.inrae.fr/trainings.html", "is_draft": false, "costs": [ "Priced" ], "topics": [ "http://edamontology.org/topic_3299", "http://edamontology.org/topic_0797", "http://edamontology.org/topic_0622" ], "keywords": [ "Genome annotation", "Comparative genomics" ], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 10, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/769/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 82, "name": "INRAE", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INRAE/?format=api" }, { "id": 88, "name": "BioinfOmics", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/BioinfOmics/?format=api" } ], "organisedByTeams": [ { "id": 10, "name": "MIGALE", "url": "https://catalogue.france-bioinformatique.fr/api/team/MIGALE/?format=api" } ], "logo_url": "https://migale.inrae.fr/sites/default/files/migale-orange_0.png", "updated_at": "2026-02-12T10:45:53.661422Z", "audienceTypes": [ "Professional (continued)" ], "audienceRoles": [ "Biologists", "Bioinformaticians" ], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "Connaître les concepts et les principales méthodes bioinformatiques pour annoter automatiquement et comparer un jeu de données de génomes bactériens. Construire et évaluer la qualité d’un jeu de données publiques. Évaluer la qualité et annoter automatiquement un jeu de données. Savoir mettre en oeuvre une comparaison de génomes et en interpréter les résultats.", "hoursPresentations": 6, "hoursHandsOn": 6, "hoursTotal": 12, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/791/?format=api" ] }, { "id": 291, "name": "Formation au logiciel R", "shortName": "Formation au logiciel R", "description": "Introduction au logiciel R et à son utilisation pour réaliser des graphiques et faire des analyses statistiques basiques en biologie. Introduction aux bibliothèques R utiles en biologie.", "homepage": "http://www.prabi.fr/spip.php?article273", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 14, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [ { "id": 19, "name": "PRABI-AMSB", "url": "https://catalogue.france-bioinformatique.fr/api/team/PRABI-AMSB/?format=api" } ], "logo_url": null, "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [ "Professional (initial)" ], "audienceRoles": [ "Life scientists" ], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "- Acquérir les compétences nécessaires à l’utilisation du logiciel R\r\n- Connaître les principales analyses statistiques nécessaires en biologie et les utiliser sous R\r\n- Réaliser des graphiques sous R\r\n- Connaitre les bibliothèques R utiles en Biologie", "hoursPresentations": 9, "hoursHandsOn": 12, "hoursTotal": 21, "personalised": false, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/437/?format=api" ] }, { "id": 362, "name": "Analyse statistique de données RNA-Seq - Recherche des régions d’intérêt différentiellement exprimées", "shortName": "Analyse statistique de données RNA-Seq", "description": "Objectifs pédagogiques\r\n* Se sensibiliser aux concepts et méthodes statistiques pour l’analyse de données transcriptomiques de type RNA-Seq.\r\n* Comprendre le matériel et méthodes (normalisation et tests statistiques) d’un article.\r\n* Réaliser une étude transcriptomique avec R dans l’environnement RStudio.\r\n\r\nProgramme\r\n* Planification expérimentale des expériences RNA-Seq (identification des biais, répétitions, biais contrôlables).\r\n* Normalisation et analyse différentielle : recherche de “régions d’intérêt” différentiellement exprimées (modèle linéaire généralisé).\r\n*Prise en compte de la multiplicité des tests.\r\n\r\nLe cours sera illustré par différents exemples. Un jeu de données à deux facteurs sera analysé avec les packages R DESeq2 et edgeR dans l’environnement RStudio.", "homepage": "https://documents.migale.inrae.fr/trainings.html", "is_draft": false, "costs": [ "Priced" ], "topics": [ "http://edamontology.org/topic_0203", "http://edamontology.org/topic_3170", "http://edamontology.org/topic_3308" ], "keywords": [ "Statistical differential analysis", "RNA-seq" ], "prerequisites": [ "Basic knowledge of R" ], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 10, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/769/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 82, "name": "INRAE", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INRAE/?format=api" }, { "id": 88, "name": "BioinfOmics", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/BioinfOmics/?format=api" } ], "organisedByTeams": [ { "id": 10, "name": "MIGALE", "url": "https://catalogue.france-bioinformatique.fr/api/team/MIGALE/?format=api" } ], "logo_url": "https://migale.inrae.fr/sites/default/files/migale-orange_0.png", "updated_at": "2024-01-18T14:50:06.093352Z", "audienceTypes": [ "Professional (continued)" ], "audienceRoles": [ "Biologists", "Bioinformaticians" ], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "Objectifs pédagogiques :\r\nSe sensibiliser aux concepts et méthodes statistiques pour l’analyse de données transcriptomiques de type RNA-Seq.\r\nComprendre le matériel et méthodes (normalisation et tests statistiques) d’un article.\r\nRéaliser une étude transcriptomique avec R dans l’environnement RStudio.", "hoursPresentations": 4, "hoursHandsOn": 8, "hoursTotal": 12, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/786/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/587/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/695/?format=api" ] }, { "id": 379, "name": "Manipulating & Visualizing Data with R", "shortName": "R - DataViz", "description": "Objectifs\r\n- Importer, structurer, transformer et exporter un tableau de données avec R\r\n- Générer des figures de qualité pour, par exemple, une publication scientifique\r\n\r\nProgramme\r\n- Introduction au tidyverse (metapackage pour manipuler, visualiser et analyser des données)\r\n- Import et export de tableaux de données (csv, excel, google sheet, etc.)\r\n- Manipulation de tableaux de données avec dplyr et tidyr (filtre, aggregation, jointure)\r\n- Manipulation de chaînes de caractères et de dates avec stringr et lubridate\r\n- Introduction aux concepts de visualisation de données\r\n- Apprendre à utiliser ggplot2 grâce à esquisse\r\n- Partager ses résultats avec Quarto", "homepage": "https://abims.sb-roscoff.fr/module/r_dataviz", "is_draft": false, "costs": [ "Free" ], "topics": [ "http://edamontology.org/topic_0092" ], "keywords": [], "prerequisites": [], "openTo": "Everyone", "accessConditions": "Preregistration required using: https://abims.sb-roscoff.fr/ateliers/preinscription", "maxParticipants": 18, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/299/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [ { "id": 4, "name": "ABiMS", "url": "https://catalogue.france-bioinformatique.fr/api/team/ABiMS/?format=api" } ], "logo_url": "https://abims.sb-roscoff.fr/sites/default/files/abims.png", "updated_at": "2026-02-05T08:15:08.934519Z", "audienceTypes": [ "Undergraduate", "Graduate", "Professional (initial)", "Professional (continued)" ], "audienceRoles": [ "All" ], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": 2, "hoursHandsOn": 5, "hoursTotal": 7, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/619/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/716/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/795/?format=api" ] }, { "id": 268, "name": "EBAII - Ecole de Bioinformatique niveau débutant", "shortName": "EBAII", "description": "Description : La formation EBAII IFB Aviesan de niveau 1 propose une expérience d'apprentissage intensive conçue pour les biologistes, qu'ils soient ingénieurs, doctorants, chercheurs, enseignants-chercheurs ou praticiens, qui sont confrontés à l'analyse de données NGS (Next-Generation Sequencing) mais qui ne disposent pas encore des compétences bioinformatiques nécessaires, ou qui cherchent à renforcer leurs compétences existantes.\r\n\r\nContenu : Cette formation est structurée autour d'une combinaison de sessions théoriques et d'ateliers pratiques. Les participants auront l'occasion d'explorer diverses thématiques, notamment le traitement de données de variants, ChIP-Seq, Bulk RNA-Seq, et Single-Cell RNA-Seq. De plus, ils recevront une introduction aux technologies \"long reads\".\r\n\r\nObjectifs généraux:\r\nAcquérir une compréhension approfondie des concepts liés à l'analyse de données NGS.\r\nMaîtriser les outils informatiques nécessaires pour effectuer ces analyses.\r\nInterpréter les résultats des analyses de données NGS.", "homepage": "https://moodle.france-bioinformatique.fr/course/view.php?id=28", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [ "Biostatistics", "Sequence analysis", "NGS Sequencing Data Analysis" ], "prerequisites": [], "openTo": "Everyone", "accessConditions": "La formation s’adresse à des biologistes directement impliqués dans des projets “Next Generation Sequencing” (NGS). \r\nAucune connaissance préalable des environnements Linux ou R n’est requise, mais il sera demandé aux participants de suivre une autoformation en ligne en amont, pour faciliter la prise en main de ces langages. 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"https://catalogue.france-bioinformatique.fr/api/event/645/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/760/?format=api" ] }, { "id": 304, "name": "Initiation à Galaxy", "shortName": "Bilille Galaxy Init", "description": "Bilille organise régulièrement des formations d'initiation à l'outil Galaxy d'une journée, destinée aux biologistes et médecins désirant découvrir le traitement bioinformatique de données via une interface conviviale.\r\n\r\nGalaxy est très répandu pour l’analyse de données omiques, telles que données de séquençage ou données de puces à ADN. \r\nC'est l'environnement qui est utilisé lors du cycle de formation “Analyse de données de séquençage à haut-débit”.", "homepage": "https://bilille.univ-lille.fr/training/training-offer", "is_draft": false, "costs": [ "Free" ], "topics": [], "keywords": [ "Galaxy" ], "prerequisites": [], "openTo": "Everyone", "accessConditions": "Ouvert en priorité aux participants du cycle Analyse NGS organisé par Bilille.", "maxParticipants": null, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/763/?format=api", "https://catalogue.france-bioinformatique.fr/api/userprofile/487/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [ { "id": 3, "name": "Bilille", "url": "https://catalogue.france-bioinformatique.fr/api/team/Bilille/?format=api" } ], "logo_url": "https://bilille.univ-lille.fr/fileadmin/_processed_/9/2/csm_logo_bilille_complet_65be9bda8b.png", "updated_at": "2024-12-09T17:41:37.266949Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/741/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/676/?format=api" ] }, { "id": 300, "name": "Analyse des données RNA-Seq sous l’environnement Galaxy", "shortName": "Analyse des données RNA-Seq sous l’environnement Galaxy", "description": "Introduction à l'analyse des données RNA-Seq sous l’environnement Galaxy", "homepage": "http://www.prabi.fr/spip.php?article274", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 14, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 9, "name": "PRABI", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/PRABI/?format=api" } ], "organisedByTeams": [ { "id": 19, "name": "PRABI-AMSB", "url": "https://catalogue.france-bioinformatique.fr/api/team/PRABI-AMSB/?format=api" } ], "logo_url": null, "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [ "Professional (continued)" ], "audienceRoles": [ "Life scientists" ], "difficultyLevel": "", "trainingMaterials": 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distance\r\n- Maximum de vraisemblance\r\n- Reconstruction phylogénétique Bayésienne\r\n- Bootstraps et autres supports de branches", "homepage": "", "is_draft": false, "costs": [ "1200 €" ], "topics": [ "http://edamontology.org/topic_3299", "http://edamontology.org/topic_0084", "http://edamontology.org/topic_3293" ], "keywords": [], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 12, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/241/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 1, "name": "CNRS formation entreprises", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/CNRS%20formation%20entreprises/?format=api" } ], "organisedByTeams": [ { "id": 7, "name": "ATGC", "url": "https://catalogue.france-bioinformatique.fr/api/team/ATGC/?format=api" } ], "logo_url": "https://ressources.france-bioinformatique.fr/sites/default/files/ATGClogox120_0.png", "updated_at": "2023-01-24T10:44:55.936489Z", "audienceTypes": [ "Professional (continued)" ], "audienceRoles": [], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "To know how to infer a phylogenetic tree and interpret it.", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": true, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/460/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/509/?format=api" ] }, { "id": 384, "name": "EBAII - Ecole de Bioinformatique niveau intermédiaire", "shortName": "EBAII N2", "description": "Objectifs: L’école s’articulera autour de trois ateliers thématiques en session parallèle (RNA-seq, ChIP-seq, variants DNA-seq), et abordera la visualisation et l’intégration des données. \r\n\r\nEnvironnement de travail: L’ensemble de la formation reposera sur l’utilisation de commandes en ligne (terminal Linux) et du langage R. \r\n\r\nPrérequis: Les candidats doivent avoir acquis les compétences enseignées durant l’école de niveau débutant: un niveau de base en ligne de commande, R, et (au choix) RNA-seq, ChIP-seq ou variants DNA-seq.", "homepage": "", "is_draft": false, "costs": [ "Priced" ], "topics": [ "http://edamontology.org/topic_3391", "http://edamontology.org/topic_3366", "http://edamontology.org/topic_0092", "http://edamontology.org/topic_3168", "http://edamontology.org/topic_0091" ], "keywords": [ "Biostatistics", "Sequence analysis", "NGS Sequencing Data Analysis" ], "prerequisites": [], "openTo": "Everyone", "accessConditions": "La formation s’adresse à des biologistes directement impliqués dans des projets “Next Generation Sequencing” (NGS) avec un niveau de base en ligne de commande, R, et (au choix) RNA-seq, ChIP-seq ou variants DNA-seq.", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "https://www.sb-roscoff.fr/sites/www.sb-roscoff.fr/files/styles/large/public/images/station-biologique-roscoff-roscoff-4404.jpg", "updated_at": "2024-12-05T07:33:48.573507Z", "audienceTypes": [], "audienceRoles": [ "Biologists" ], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/644/?format=api" ] }, { "id": 396, "name": "Metagenomics and Metatranscriptomics initiation", "shortName": "Metagenomics", "description": "Présentation de la formation\r\nA la demande du laboratoire d'Ecologie Microbienne de Lyon, l'équipe Formation de l'IFB organise une session de formation de deux jours sous Galaxy pour l'analyse de données de métagénomique et métatranscriptomique.\r\n\r\nObjectifs pédagogiques\r\nA la fin de cette formation, les participants 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key steps in RNASeq data analysis for a differential expression study\r\n- Know how to perform command-line analysis using Snakemake.\r\n\r\nPedagogical Content\r\nDay 1\r\n- Principle of RNASeq technology: objectives and experimental design.\r\n- Data quality assessment (FastQC, MultiQC).\r\n- Sequence alignment to a reference genome (STAR).\r\n\r\nDay 2\r\n- Differential gene expression analysis (HTSeqCount, DESeq2).\r\n- Functional annotation (GO, Kegg).\r\n- Using the Snakemake workflow system.\r\n- Comparison between RNASeq and 3’SRP methods.\r\n\r\nThe theoretical part is followed by a pipeline run step-by-step on a test dataset. \r\nIt will be possible to start an analysis on your own data.", "homepage": "https://pf-bird.univ-nantes.fr/training/rnaseq/", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Everyone", "accessConditions": "- Be comfortable with basic Linux commands or have completed the training course 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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. 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