Training List
Handles creating, reading and updating training events.
GET /api/training/?format=api&offset=200&ordering=-homepage
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"https://mesocentre.uca.fr/medias/photo/logoaubi-2019minus_1553844844490-jpg?ID_FICHE=41175", "updated_at": "2024-02-08T11:28:41.024508Z", "audienceTypes": [ "Undergraduate", "Graduate", "Professional (initial)", "Professional (continued)" ], "audienceRoles": [ "Researchers", "Life scientists", "Biologists" ], "difficultyLevel": "Novice", "trainingMaterials": [ { "id": 134, "name": "Nucleoli segmentation and feature extraction using CellProfiler", "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/Nucleoli%20segmentation%20and%20feature%20extraction%20using%20CellProfiler/?format=api" } ], "learningOutcomes": "At the end, learners would be able to:\r\n- How to download images from a public image repository.\r\n- How to segment cell nuclei using CellProfiler in Galaxy.\r\n- How to segment cell nucleoli using CellProfiler in Galaxy.\r\n- How to extract features for images, nuclei and nucleoli.", "hoursPresentations": 1, "hoursHandsOn": 2, "hoursTotal": 3, 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[], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [] }, { "id": 13, "name": "Formation interne pipeline DEVA detection de variants par NGS", "shortName": "", "description": "", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "NGS Data Analysis" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [] }, { "id": 11, "name": "Bioinformatique, NGS et Cancer", "shortName": "", "description": "Co-organisation Atelier Cancéropole Ile de France « Bioinformatique, NGS et Cancer» (avril 2014 et Nov 2014)\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "NGS Data Analysis" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "http://www.canceropole-idf.fr/fr/ngs\n", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [] }, { "id": 195, "name": "NGS et Cancer (Canceropôle) : 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"", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "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/321/?format=api" ] }, { "id": 8, "name": "DU \"séquençage haut débit et maladies génétiques\"", "shortName": "", "description": "Acquérir une formation en séquençage nouvelle génération appliqué aux maladies génétiques mendéliennes,des technologies de séquençage et approches expérimentales possibles aux outils bio-informatiques utilisés pour le traitement des données brutes, l'identification de variations génétiques et l'interprétation des résultats. Se familiariser avec le système Unix/Linux, la ligne de commande et la gestion et l'analyse de données sur un serveur à distance. Connaître et savoir utiliser les principaux logiciels dédiés à l'analyse de données de séquençage nouvelle génération, de l'alignement des séquences brutes à l'annotation de variations génétiques. Maîtriser les principaux navigateurs, bases de données et outils de prédiction couramment utilisés en génétique humaine et médicale. Connaître les différentes applications possibles du séquençage nouvelle génération pour le diagnostic de maladies génétiques, les principales règles à suivre et paramètres à considérer pour assurer la qualité des données produites dans un contexte de laboratoire médical, et les considérations éthiques que soulève le séquençage nouvelle génération pour l'interprétation et le rendu des résultats.\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [], "prerequisites": [ "Autre (Diplôme universitaire, école d'ingénieur ...)" ], "openTo": "Internal personnel", "accessConditions": "Aucune\n", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [] }, { "id": 372, "name": "Introduction à l'analyse d’images avec Galaxy", "shortName": "", "description": "L’objectif de cette formation est de se familiariser avec les premières étapes à l’analyse d’images. 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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. 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