Training List
Handles creating, reading and updating training events.
GET /api/training/?format=api&offset=200&ordering=-openTo
{ "count": 378, "next": "https://catalogue.france-bioinformatique.fr/api/training/?format=api&limit=20&offset=220&ordering=-openTo", "previous": "https://catalogue.france-bioinformatique.fr/api/training/?format=api&limit=20&offset=180&ordering=-openTo", "results": [ { "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": 194, "name": "NGS et Cancer (Canceropôle) : Analyse DNASeq", "shortName": "", "description": "", "homepage": "", "is_draft": false, "costs": [ "Free" ], "topics": [], "keywords": [], "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": [ "https://catalogue.france-bioinformatique.fr/api/event/321/?format=api" ] }, { "id": 195, "name": "NGS et Cancer (Canceropôle) : Analyse A-RNASeq", "shortName": "", "description": "", "homepage": "", "is_draft": false, "costs": [ "Free" ], "topics": [], "keywords": [], "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": [ "https://catalogue.france-bioinformatique.fr/api/event/322/?format=api" ] }, { "id": 295, "name": "Introduction to the use of a computing cluster", "shortName": "", "description": "Knowledge of the concepts and best practices for using the computing resources of the mesocenter cluster Clermont Auvergne in a bioinformatics context.\r\nBecome familiar with the work environment of the computing cluster, become autonomous in the use of its resources and learn to use a scheduler. \r\nPresentation of the resources accessible on the cluster (computing nodes, storage spaces, tools).\r\nConcept of jobs, queues and parallel computing.\r\nJob management (submission, follow-up, deletion).", "homepage": "https://mesocentre.uca.fr/", "is_draft": false, "costs": [ "Free to academics" ], "topics": [ "http://edamontology.org/topic_0091", "http://edamontology.org/topic_0605" ], "keywords": [], "prerequisites": [ "Linux and knowledge of NGS formats" ], "openTo": "Internal personnel", "accessConditions": "Have an account on the Mesocentre UCA computing cluster (make a request if necessary on the site https://hub.mesocentre.uca.fr)\r\nAlternation of theoretical courses and practical work.\r\nCOME WITH A LAPTOP with an operational Eduroam connection.\r\nThe training is in French.", "maxParticipants": 10, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 45, "name": "UMR 454 MEDIS INRA-Université Clermont Auvergne", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/UMR%20454%20MEDIS%20INRA-Universit%C3%A9%20Clermont%20Auvergne/?format=api" } ], "organisedByTeams": [ { "id": 31, "name": "AuBi", "url": "https://catalogue.france-bioinformatique.fr/api/team/AuBi/?format=api" } ], "logo_url": null, "updated_at": "2023-01-24T10:21:58.347905Z", "audienceTypes": [ "Graduate" ], "audienceRoles": [ "Researchers", "Computer scientists" ], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": 3, "hoursHandsOn": 4, "hoursTotal": 8, "personalised": false, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/487/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/616/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/461/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/708/?format=api" ] }, { "id": 157, "name": "Cycle « Initiation à la bioinformatique » - Module 4/4 : Initiation à la reconstruction phylogénétique en biologie moléculaire", "shortName": "", "description": "Bilille propose un cycle de découverte de la bioinformatique à destination des chercheur·euses, enseignant·es-chercheur·euses, ingénieur·es, technicien·nes et doctorant·es en biologie. Aucun pré-requis en informatique n'est attendu.\r\nLe cycle est constitué de quatre modules de deux jours:\r\n- Banques de données et BLAST\r\n- Alignement de séquences\r\n- Prédiction de gènes et annotation de protéines\r\n- Initiation à la reconstruction phylogénétique en biologie moléculaire\r\nCes modules peuvent être suivis indépendamment, mais ont une cohérence. Suivre chaque module peut aider à une meilleure compréhension des modules suivants.\r\nLes fiches descriptives des différents modules sont accessibles sur le site web de Bilille.\r\nLes objectifs du module 4 sont :\r\n- Comprendre les grands principes de l’évolution moléculaire et de la reconstruction phylogénétique\r\n- Savoir construire des alignements informatifs pour une analyse phylogénétique\r\n- Comprendre les modèles phylogénétiques probabilistes, les méthodes d'inférence et savoir les appliquer\r\n- Savoir reconstruire des arbres phylogénétiques en Maximum de vraisemblance (ML) et par Inférence Bayésienne (BI)\r\n- Etre capable d’analyser avec un regard critique les résultats obtenus", "homepage": "https://bilille.univ-lille.fr/training/training-offer", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Phylogeny", "Evolution and Phylogeny", "Molecular evolution", "Speciation dating", "Tree of Life", "Sequence analysis", "Multiple sequence alignment" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "- Il est conseillé mais non nécessaire d’avoir suivi le module 1/4 « Banques de données et Blast » et le module 2/4 « Alignements de séquences » du cycle d'initiation à la bioinformatique.", "maxParticipants": null, "contacts": [], "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": "2024-12-09T17:41:54.833188Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [] }, { "id": 10, "name": "Formations Universitaire", "shortName": "", "description": "\nOrganisatrice et responsable du module « cellule épithéliale et cancer » de l’option B2PCR du M2 BCPP (Biologie Cellulaire, Physiologie et Pathologies : Université Paris 5, 11 et 12 (depuis 2010).\nCours et jury M1 et M2R Magistère Européen de Génétique – UE Génétique Moléculaire des Maladies Génétiques (depuis 2011).\n\n", "homepage": "http://www.france-bioinformatique.fr", "is_draft": false, "costs": [], "topics": [], "keywords": [], "prerequisites": [ "Master" ], "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": 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": 209, "name": "Initiation à Python", "shortName": "", "description": "", "homepage": "", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [], "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": [ "https://catalogue.france-bioinformatique.fr/api/event/338/?format=api" ] }, { "id": 303, "name": "Tools for phylogenetic analysis", "shortName": "", "description": "You will learn How to find homologs, make multiple alignments, reconstruct the phylogeny, visualize the tree.\r\n\r\nAt the end of the workshop, you will be able to use web tools to reconstruct accurate phylogenies.\r\n\r\nUnless all participants speak French, the course will be taught in English.", "homepage": "https://pliniuscursus.univ-amu.fr/formation/tools-for-phylogenetic-analysis/", "is_draft": false, "costs": [ "Free to academics" ], "topics": [ "http://edamontology.org/topic_0084" ], "keywords": [], "prerequisites": [ "Master" ], "openTo": "Internal personnel", "accessConditions": "The first sessions are only available for IM2B students.", "maxParticipants": 10, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 38, "name": "IGS - Laboratoire Information Génomique et Structurale", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/IGS%20-%20Laboratoire%20Information%20G%C3%A9nomique%20et%20Structurale/?format=api" } ], "organisedByTeams": [ { "id": 23, "name": "PACA-Bioinfo", "url": "https://catalogue.france-bioinformatique.fr/api/team/PACA-Bioinfo/?format=api" } ], "logo_url": null, "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [ "Graduate" ], "audienceRoles": [ "Biologists" ], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": 1, "hoursHandsOn": 5, "hoursTotal": 6, "personalised": null, "event_set": [] }, { "id": 373, "name": "Introduction à la segmentation des nucléoles et extraction de caractéristiques avec Galaxy", "shortName": "", "description": "L’objectif de cette formation est de se familiariser avec les premières étapes à l’analyse d’images. Nous proposons au personnel non-bioinformaticien de les accompagner dans la prise en main des ces étapes d’analyses en utilisant la plateforme de bio-analyse Galaxy. \r\n\r\nAprès une introduction à l’analyse d’images, une session pratique sur la plateforme Galaxy couvrira comment :\r\n- télécharger des images depuis un répertoire d’images publiques,- segmenter une image\r\n- extraire les caractéristiques des images", "homepage": "", "is_draft": false, "costs": [ "Free to academics" ], "topics": [ "http://edamontology.org/topic_3383", "http://edamontology.org/topic_3382" ], "keywords": [ "Galaxy" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "Formation ouverte au personnel de l’UCA & Associés\r\nAvoir un ordinateur portable et un accès wifi eduroam\r\nAvoir un compte sur la plateforme Galaxy (Faire une demande le cas échéant sur hub.mesocentre.uca.fr)\r\nÊtre familier avec Galaxy", "maxParticipants": null, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/261/?format=api", "https://catalogue.france-bioinformatique.fr/api/userprofile/677/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [ { "id": 1, "name": "CNRS - IFB", "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/CNRS%20-%20IFB/?format=api" }, { "id": 16, "name": "Université Clermont Auvergne", "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/Universit%C3%A9%20Clermont%20Auvergne/?format=api" } ], "organisedByOrganisations": [ { "id": 96, "name": "Mésocentre Clermont-Auvergne", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/M%C3%A9socentre%20Clermont-Auvergne/?format=api" }, { "id": 87, "name": "AuBi", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/AuBi/?format=api" } ], "organisedByTeams": [ { "id": 31, "name": "AuBi", "url": "https://catalogue.france-bioinformatique.fr/api/team/AuBi/?format=api" } ], "logo_url": "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, "personalised": null, "event_set": [] }, { "id": 15, "name": "IFSBM", "shortName": "", "description": "\nUFR médecine Paris-Sud (mai 2015). Big data en médecine. Acquisition et analyse des données de haut débit dans le but de détecter des variants génomiques (CGH, exome, génome), étudier les profils d’expression ou le statut épigénétique des cellules (expression array, RNA-seq, ChiP-seq, medip-seq).\n \nUFR médecine Paris-Sud (janvier 2015) Méthodologie en biologie moléculaire et cellulaire et analyse d’article\n\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [], "prerequisites": [ "Autre (Diplôme universitaire, école d'ingénieur ...)" ], "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": 39, "name": "Introduction to bioinformatics for 1st year Master in integrative Plant Biology, Strasbourg University", "shortName": "", "description": "2H / year of hands-on introduction to bioinformatics for 1st year Master in integrative Plant Biology, Strasbourg University\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [], "prerequisites": [ "Master (M1 uniquement)" ], "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": 40, "name": "Formation ABiMS", "shortName": "", "description": "L'offre de formation repose sur des modules de formation d'initiation aux environnements (Linux, Cluster, etc.), d'utilisation des outils (Galaxy, etc.) et langages (PERL, R, etc.), et de compréhension des méthodes (RNA-seq, Analyses statistiques, etc.). ABiMS est également en mesure de proposer des formations à façon pour des communautés (e.g. Métabolomique) ou des projets (École thématique).\nUniversitaires.\n \nGalaxy pour l'analyse de données métabolomique (1 jour)\nCluster (1 jour)\nLinux Initiation (1 jour)\nLinux avancé (1 jour)\nLinux scripting (1 jour)\nGalaxy initiation (1 jour)\nGalaxy RNAseq de novo/avec référence & cleaning (2 jours)\nGalaxy : initiation à la phylogénie (2 jours)\nR initiation (1 jour)\nR avancé (1 jour)\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Autre" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "Ouvert à tous avec facturation\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": 150, "name": "Cycle « Analyse de données de séquençage à haut-débit » - Module 4/5 : Analyses RNA-seq - partie 2 (biostatistique)", "shortName": "", "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 5 modules, à la carte : \r\n- Module 1: Analyses ADN\r\n- Module 2: Analyses de variants\r\n- Module 3: Analyses RNA-seq, bioinformatique\r\n- Module 4: Analyses RNA-seq, biostatistique\r\n- Module 5: Métagénomique\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 4 sont :\r\n- Savoir réaliser une analyse différentielle de données RNA-seq à partir d’une table de comptage (quantifiant les lectures alignées) à l’aide du portail Galaxy\r\n- Avoir un regard critique sur les résultats d’une analyse différentielle\r\n- Comprendre différentes méthodes de normalisation et les contextes d’utilisation correspondants", "homepage": "https://bilille.univ-lille.fr/training/training-offer", "is_draft": false, "costs": [], "topics": [], "keywords": [ "NGS Data Analysis", "Transcriptomics (RNA-seq)", "NGS Sequencing Data Analysis" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "- Etre familier avec la plate-forme web Galaxy (idéalement avoir suivi la formation bilille « Initiation à Galaxy »)\r\n- Avoir suivi le module 2/5 «Analyses RNA-seq–partie 1 (bioinformatique)» de ce cycle ou toute autre formation permettant de justifier de connaissances sur les données de séquençage haut débit et la façon d’obtenir une table de comptage", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 66, "name": "University of Lille", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/University%20of%20Lille/?format=api" }, { "id": 56, "name": "INSERM", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INSERM/?format=api" }, { "id": 52, "name": "CNRS", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/CNRS/?format=api" } ], "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": "2024-12-09T17:42:50.474644Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/279/?format=api" ] }, { "id": 4, "name": "Introduction to data analysis with R", "shortName": "", "description": "The program includes an introduction:\nApproaches in biostatistics and research, explaining to participants the principles, methodologies, use of statistical methods and applications in biology and clinical research.\nCourses on software R will be delivered in the form of additional exercises. The basis of the programming language R will be discussed and statistical approaches presented in the theoretical part will be implemented.\nApplication of skills acquired over a personal dataset\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Programming Languages & Computer Sciences", "R Language" ], "prerequisites": [], "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": 5, "name": "Partek Workshop", "shortName": "", "description": "Introduction to Partek® software and the principles of RNA-seq data analysis DNA-Seq analysis and annotations with Partek® Genomics Suite® Hands on analysis in Partek® Flow® including: Data import and sample annotation, Pre and post alignment quality control, Gene and transcript quantification, Detection of differential expression using powerful gene specific modeling\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Bioinformatics & Biomedical" ], "prerequisites": [], "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": 6, "name": "Ingenuiy Pathways Analysis Workshop", "shortName": "", "description": "The User Group Meeting will consist of talks, customer case studies and interactive feedback sessions where new and existing users of QIAGEN’s Ingenuity products can learn about product updates, usability tips & tricks and best practices. Take advantage of this opportunity to engage with other users from the scientific community.\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Bioinformatics & Biomedical" ], "prerequisites": [], "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": 16, "name": "Formations à la plate-forme Microscope", "shortName": "", "description": "The LABGeM team at Genoscope regularly organizes training courses dedicated to the analysis of bacterial genomes via the use of the MicroScope platform at the University of Évry.\n \nThe course \"Annotation and analysis of prokaryotic genomes using the MicroScope platform\" lasting 4.5 days is aimed at:\nacquiring theoretical and practical knowledge of genome annotation tools (structural and functional annotation, metabolic networks annotation)\nknowing how to interpret the results of functional annotation tools\nknowing how to carry out various comparative analyzes: analyzes of conserved syntenia, pan-genomes, phylogenetic and metabolic profiles\nlearning to interpret the results of metabolic network prediction tools and search for candidate genes for enzymatic activities\napplying those tools to the analysis of genomes of interest to the participants \nEach session is made up of half theory and half practical work. During the training, participants have the opportunity to work on their own data during practical work.\n \nThis training is aimed at doctoral students, engineers, researchers, experienced biological or medical laboratory technicians. 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