Training List
Handles creating, reading and updating training events.
GET /api/training/?format=api&offset=160&ordering=-contacts
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La formation abordera les différents points fondamentaux (théoriques, pratiques, juridiques) en lien avec la politique nationale d’ouverture des données de la recherche et présentera sous forme de séances pratiques les ressources nationales accessibles à la communauté scientifique ainsi que les solutions proposées par l’IFB pour gérer les données d’un projet de recherche.", "homepage": "https://ifb-elixirfr.github.io/IFB-FAIR-data-training/", "is_draft": false, "costs": [ "Free" ], "topics": [ "http://edamontology.org/topic_3420", "http://edamontology.org/topic_3571", "http://edamontology.org/topic_0219" ], "keywords": [ "Données" ], "prerequisites": [], "openTo": "Everyone", "accessConditions": "public", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [ { "id": 3, "name": "IFB", "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/IFB/?format=api" } ], "organisedByOrganisations": [ { "id": 43, "name": "IFB-core", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/IFB-core/?format=api" } ], "organisedByTeams": [ { "id": 29, "name": "IFB Core", "url": "https://catalogue.france-bioinformatique.fr/api/team/IFB%20Core/?format=api" } ], "logo_url": "https://www.france-bioinformatique.fr/wp-content/uploads/logo-ifb-couleur.svg", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "A la fin de cette formation, les participants connaîtront et pourront mettre en œuvre les principes de la science ouverte pour gérer leurs jeux de données dans un projet :\r\n- Les principes fondamentaux de l’Open Data en biologie et santé, y compris dans ses aspects juridiques ;\r\n- Les bonnes pratiques et outils de gestion des données d’un projet en bioinformatique, en lien avec les ressources de l’infrastructure IFB ;\r\n- Le PGD : séances théoriques et pratiques de construction d’un PGD sur des exemples de jeux de données omiques ;\r\n- Le choix des métadonnées : panorama des ressources existantes pour choisir des métadonnées et mise en pratique pour annoter des jeux de données omiques en vue de la publication des données dans une banque internationale ou un dataverse institutionnel.", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": false, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/418/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/404/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/465/?format=api" ] }, { "id": 213, "name": "Analyse bioinformatique de données RNA-Seq sous Galaxy", "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/342/?format=api" ] }, { "id": 321, "name": "Genopole Autumn School", "shortName": "", "description": "Cette formation est dédiée aux chercheurs, ingénieurs et doctorants et dispensée en anglais par des experts internationaux de la génomique.\r\nLes points forts de la formation :\r\n\r\n Des sessions de formation pratiques aux outils d’analyse génomique\r\n Des experts des grands centres nationaux et internationaux (Université d’Evry – Paris-Saclay, Inrae, CEA, CNRS, Université du Luxembourg, EMBL-EBI)\r\n Format résidentiel tout inclus dans un cadre accueillant et propice au networking\r\n Effectif limité à 15 participants pour une qualité optimale des sessions pratiques\r\n Formation éligible à la prise en charge employeurs ou OPCO", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": null, "updated_at": "2022-11-14T16:38:22.898523Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/501/?format=api" ] }, { "id": 276, "name": "Introduction to Machine Learning Using R", "shortName": "", "description": "With the rise in high-throughput sequencing technologies, the volume of omics data has grown exponentially in recent times and a major issue is to mine useful knowledge from these data which are also heterogeneous in nature. Machine learning (ML) is a discipline in which computers perform automated learning without being programmed explicitly and assist humans to make sense of large and complex data sets. The analysis of complex high-volume data is not trivial and classical tools cannot be used to explore their full potential. Machine learning can thus be very useful in mining large omics datasets to uncover new insights that can advance the field of bioinformatics.\r\n\r\nThis 2-day course will introduce participants to the machine learning taxonomy and the applications of common machine learning algorithms to omics data. The course will cover the common methods being used to analyse different omics data sets by providing a practical context through the use of basic but widely used R libraries. The course will comprise a number of hands-on exercises and challenges where the participants will acquire a first understanding of the standard ML processes, as well as the practical skills in applying them on familiar problems and publicly available real-world data sets.", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 30, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 8, "name": "Elixir", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/Elixir/?format=api" }, { "id": 4, "name": "IFB - ELIXIR-FR", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/IFB%20-%20ELIXIR-FR/?format=api" } ], "organisedByTeams": [ { "id": 29, "name": "IFB Core", "url": "https://catalogue.france-bioinformatique.fr/api/team/IFB%20Core/?format=api" } ], "logo_url": "https://www.dissco.eu/wp-content/uploads/Elixir-Europe-logo-1.png", "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/415/?format=api" ] }, { "id": 64, "name": "Read alignment and SNP calling", "shortName": "", "description": "This training session, organized jointly with the Sigenae platform, is designed to help you deal with NGS data, in particular Roche 454 and Illumina Solexa technologies. You will discover the new sequence formats, the new assembly formats and the known biases of these technologies. You will use mapping on reference genome software, polymorphisms detection (with the GATK pipeline), polymorphisms annotation and alignment visualization software. Organized jointly by the Sigenae and bioinfo genotoul platforms.\n", "homepage": "http://bioinfo.genotoul.fr/index.php/events/alignment-and-small-size-variants-ca…", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [ "NGS Data Analysis", "Variant analysis", "Genomics (DNA-seq)" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "You need to register (via the website) and pay 165 euros a day for academic and 550 euros a day for a private.\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": 119, "name": "Modules Biologie École Doctorale SVSAE", "shortName": "", "description": "Les UE de bioinformatique de la spécialité AMD sont ouvertes aux doctorants de l'école doctorale SVSAE dans le cadre de leur formation doctorale. 3 UE sont particulièrement suivies : UE « Programmation en perl », UE « Bioistatistiques et programmation sous R » et UE « Génomique et bioinformatique ». Les formations continues proposées dans le domaine de la bioinformatique sont également ouvertes aux étudiants de l'Ecole Doctorale, et permettent de valider un module de biologie. Forme 2 à 3 doctorants par an.\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": 247, "name": "Manual curation of Transposable element annotation", "shortName": "", "description": "URGI organizes a BYOD-style (Bring Your Own Data) training course on manual curation of transposable elements reference sequences obtained with REPET pipelines.\n", "homepage": "https://urgi.versailles.inra.fr/Platform/Training/Manual-curation-of-Transposabl…", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "https://ressources.france-bioinformatique.fr/sites/default/files/Capture%20d%E2%80%99e%CC%81cran%202018-12-05%20a%CC%80%2009.40.29_0.png", "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/379/?format=api" ] }, { "id": 248, "name": "RNaseq with Galaxy ", "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/380/?format=api" ] }, { "id": 67, "name": "RNAseq de novo assembly", "shortName": "", "description": "This training session has been designed to give you an overview of the methods and tools used to de novo assemble transcriptomic short reads. You will learn how to pre-process your raw data (fastq files), how an assembler works and how to use it. Finally you will learn how to assess the quality of your assemblies in order to choose the best one. Organized jointly by the Sigenae and bioinfo genotoul platforms.\n", "homepage": "http://bioinfo.genotoul.fr/index.php/events/rnaseq-de-novo-assembly-2/", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [ "NGS Data Analysis", "Analysis of RNAseq data", "Transcript and transcript variant analysis", "Transcriptomics (RNA-seq)", "Sequence annotation" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "You need to register (via the website) and pay 165 euros a day for academic and 550 euros a day for a private.\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": 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": 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": 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": 275, "name": "Single-Cell : Transcriptomics, Spatial and Long reads", "shortName": "SincellTE", "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.", "homepage": "", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [], "prerequisites": [ "Master", "Autre (Diplôme universitaire, école d'ingénieur ...)" ], "openTo": "Everyone", "accessConditions": "Participants must have prior experience on NGS data analysis with everyday use of R and/or Python and good knowledge of Unix command line. Before the training, participants are advised to familiarize themselves with the processing and primary analyses steps of scRNA-seq datasets. \r\nIt is not necessary to have personal single-cell data to analyse.", "maxParticipants": 30, "contacts": [], "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": [], "logo_url": "https://ressources.france-bioinformatique.fr/sites/default/files/sincellTE_logo_0_2.png", "updated_at": "2024-03-20T09:31:42.144175Z", "audienceTypes": [], "audienceRoles": [ "Researchers", "Life scientists", "Biologists", "Bioinformaticians" ], "difficultyLevel": "Intermediate", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/199/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/405/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/422/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/177/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/606/?format=api" ] }, { "id": 14, "name": "Formation interne pipeline RNASeq", "shortName": "", "description": "", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "NGS Data Analysis", "Analysis of RNAseq data" ], "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": 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. It concerns both people who already have an annotation project on the MicroScope platform and wishing to deepen its use, as well as those wishing to learn microbial genomics.\n \n \nIn addition, if you are a user of the MicroScope platform and you have already followed the training \"Annotation and analysis of prokaryotic genomes using the MicroScope platform\" a few years ago we have implemented a new training , the \"MicroScope Platform - Advanced Course\" training in order to update your knowledge on the latest evolutions of the platform and to deepen some of its major functionalities.\n \nThis training, lasting 2 days, will consolidate your use of the platform but also go further:\nPresentation of the evolutions of the MicroScope platform\nPresentation of the new flagship features of the MicroScope platform\nPresentation of tools for RNA-seq analyzes\nDeepening of the functionalities allowing the exploration of the bacterial metabolism\n", "homepage": "https://labgem.genoscope.cns.fr/professional-trainings/microscope-professional-t…", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Methodology", "Metagenomics", "Metabolic Network Modelling", "Read alignment on genomes", "Gene expression differential analysis", "Web portals", "Variant analysis", "Interfaces", "Systems Biology", "Interoperability", "Metabolomics and Fluxomics", "Metabolic network analysis", "Genome analysis", "Structural and functional annotation of genomes", "Complete genomes", "Transcriptomics (RNA-seq)", "Genomics (DNA-seq)", "Functional and regulatory pathways comparison", "Genomes comparison", "Data collection curation", "Comparative genomics", "Data Integration", "Data management and transfer", "NGS Sequencing Data Analysis", "Toolkit", "Tool integration", "Databases and information systems", "Développements technologiques de l‘Information et de la Communication" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "For more information and registration : https://labgem.genoscope.cns.fr/professional-trainings/microscope-professional-trainings/.\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": 285, "name": "Linux Avancé / Advanced Linux", "shortName": "Advanced Linux", "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/module/linux_advanced", "is_draft": false, "costs": [ "Free" ], "topics": [ "http://edamontology.org/topic_3316" ], "keywords": [], "prerequisites": [ "Linux - Basic Knowledge" ], "openTo": "Everyone", "accessConditions": "Preregistration required using: https://abims.sb-roscoff.fr/ateliers/preinscription", "maxParticipants": 18, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 65, "name": "SBR - Roscoff Marine Station", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/SBR%20-%20Roscoff%20Marine%20Station/?format=api" } ], "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": "2026-02-03T16:16:01.381880Z", "audienceTypes": [ "Graduate", "Professional (initial)", "Professional (continued)" ], "audienceRoles": [], "difficultyLevel": "Intermediate", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": 3, "hoursHandsOn": 4, "hoursTotal": 7, "personalised": false, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/497/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/435/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/521/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/713/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/764/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/624/?format=api" ] }, { "id": 19, "name": "Analyse primaire de données issues de séquenceurs nouvelle génération sous Galaxy", "shortName": "", "description": "\nObjectifs\n\nConnaître les concepts et méthodes bioinformatiques utilisés pour l’analyse primaire de données issues de NGS. Application aux outils de mapping et d’assemblage.\nProgramme\nThéorie \n•Présentation des différents types de séquenceurs\n•Les grandes familles d’algorithmes de mapping de lectures courtes d’assemblage et les outils associés\nPratique\nAnalyse des données de séquençage d’un génome bactérien\n•Contrôle qualité\n•Assemblage de-novo\noNettoyage des données\noAssemblage\noVisualisation et statistiques sur l’assemblage\n•Comparaison à un génome de référence :\noMapping des lectures sur un génome proche\noVisualisation du mapping \n", "homepage": "http://migale.jouy.inra.fr/", "is_draft": false, "costs": [], "topics": [], "keywords": [ "NGS Data Analysis", "Galaxy", "NGS Sequencing Data Analysis" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "Ce cycle est ouvert à l'ensemble des agents de l'INRA et aux extérieurs.\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": [ "https://catalogue.france-bioinformatique.fr/api/event/246/?format=api" ] }, { "id": 156, "name": "Python for biology", "shortName": "", "description": "", "homepage": "https://cnrsformation.cnrs.fr/stage-17266-Python-pour-la-biologie.html", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [ "Sequence Algorithm", "Python Language", "Sequence analysis" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "CNRS fee-based training\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": 134, "name": "Initiation à l'analyse de données avec R", "shortName": "", "description": "Le cours s’adresse à des personnes qui veulent apprendre ou ré-apprendre à utiliser les statistiques à bon escient pour leurs propres projets. L’objectif est de présenter et expliquer les principales notions de statistiques utiles pour décrire un jeu de données, en explorer les propriétés afin d’en tirer des conclusions robustes, utiliser à bon escient les méthodes les plus courantes (tests d’hypothèse, ACP, …) et savoir lire, interpréter (et éventuellement aborder d’un œil critique) les résultats présentés dans les publications. Nous utiliserons le moins possible le formalisme mathématique mais insisterons sur les propriétés des méthodes, leurs pré-requis, l’interprétation des résultats. Nous aborderons les notions d’analyse exploratoire, ACP, clustering, estimation, échantillonnage, régression, tests d’hypothèse, planification d’expérience\nCe cours est une initiation à l’analyse de données. Il est préférable d’avoir une connaissance minimale de R. Dans le cas contraire, un tutoriel d’initiation est disponible sur la page web du cours et les notions de base de R seront rappelées pendant la pratique. Pour les personnes n’ayant jamais utilisé R, il peut être utile d’avoir des connaissances de base en programmation, quel que soit le langage.\nLes cours seront donnés en Français et alterneront théorie et pratique avec RStudio. Il est demandé à chaque participant de venir avec un ordinateur portable chargé sur lequel il aura préalablement installé les éléments nécessaires (R, Rstudio et les fichiers de données sur lesquels nous travaillerons). La liste complète des fichiers et logiciels nécessaires sera disponible sur la page web du cours une dizaine de jours avant le début de la session.\nderniere session: Mar 2016\n \n", "homepage": "https://c3bi.pasteur.fr", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Biostatistics", "Programming Languages & Computer Sciences", "Statistical Tests", "R Language", "Descriptive statistics" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "ouvert à tous, sur inscription.\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": [ "https://catalogue.france-bioinformatique.fr/api/event/534/?format=api" ] } ] }
