Training List
Handles creating, reading and updating training events.
GET /api/training/?format=api&offset=80&ordering=-shortName
{ "count": 391, "next": "https://catalogue.france-bioinformatique.fr/api/training/?format=api&limit=20&offset=100&ordering=-shortName", "previous": "https://catalogue.france-bioinformatique.fr/api/training/?format=api&limit=20&offset=60&ordering=-shortName", "results": [ { "id": 383, "name": "Artificial Intelligence and Machine Learning in Life Sciences: from foundations to applications", "shortName": "AI & ML in LS", "description": "Artificial intelligence (AI) has permeated our lives, transforming how we live and work. Over the past few years, a rapid and disruptive acceleration of progress in AI has occurred, driven by significant advances in widespread data availability, computing power and machine learning. Remarkable strides were made in particular in the development of foundation models - AI models trained on extensive volumes of unlabelled data. Moreover, given the large amounts of omics data that are being generated and made accessible to researchers due to the drop in the cost of high-throughput technologies, analysing these complex high-volume data is not trivial, and the use of classical statistics can not explore their full potential. As such, Machine Learning (ML) and Artificial Intelligence (AI) have been recognized as key opportunity areas, as evidenced by a number of ongoing activities and efforts throughout the community.\r\n\r\nHowever, beyond the technological advances, it is equally important that the individual researchers acquire the necessary knowledge and skills to fully take advantage of Machine Learning. Being aware of the challenges, opportunities and constraints that ML applications entail, is a critical aspect in ensuring high quality research in life sciences.\r\n\r\nRecognizing this need, this week-long training will bring together experts from four ELIXIR Nodes and deliver a hands-on, high-intensity course available for members from all ELIXIR Nodes.\r\n\r\nLearners will be guided across the various steps in Machine Learning, from the foundational concepts, through the deep learning and generative AI techniques, closely complemented by insights into the existing reporting (DOME Recommendations) and regulatory frameworks (EU AI Act).", "homepage": "", "is_draft": false, "costs": [], "topics": [ "http://edamontology.org/topic_3474" ], "keywords": [], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 30, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "https://www.dissco.eu/wp-content/uploads/Elixir-Europe-logo-1-300x226.png", "updated_at": "2025-01-23T14:14:17.330709Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "Intermediate", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/643/?format=api" ] }, { "id": 356, "name": "Advanced Python", "shortName": "Advanced Python", "description": "Objectifs pédagogiques\r\n\r\nA l’issue de la formation, les stagiaires seront capables de :\r\n\r\nconnaître les éléments avancés du langage de programmation Python,\r\nles appliquer sur des cas concrets en bioinformatique,\r\nêtre autonome dans la mise en place de tâches complexes visant à extraire et re-formater des données issues de fichiers textes,\r\ndans le cadre de traitement de données via le langage de programmation Python\r\n\r\nProgramme\r\n\r\nFonctions\r\nExpressions régulières\r\nGestion des erreurs\r\nBiopython\r\nQuelques modules de bioinformatique\r\nRéalisation de programmes et de Notebooks Jupyter\r\nIllustration avec des exercices de manipulation de fichiers de séquences", "homepage": "https://documents.migale.inrae.fr/trainings.html", "is_draft": false, "costs": [ "Priced" ], "topics": [ "http://edamontology.org/topic_0605" ], "keywords": [ "Python Language" ], "prerequisites": [ "Python - basic knowledge" ], "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": "2024-01-18T13:17:08.789820Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "Advanced", "trainingMaterials": [], "learningOutcomes": "A l’issue de la formation, les stagiaires seront capables de :\r\n\r\nconnaître les éléments avancés du langage de programmation Python,\r\nles appliquer sur des cas concrets en bioinformatique,\r\nêtre autonome dans la mise en place de tâches complexes visant à extraire et re-formater des données issues de fichiers textes,\r\ndans le cadre de traitement de données via le langage de programmation Python", "hoursPresentations": 2, "hoursHandsOn": 10, "hoursTotal": 12, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/575/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/788/?format=api" ] }, { "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/624/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/764/?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": 140, "name": "Bioinformatique et Analyses Mutationnelles", "shortName": "", "description": "Module de formation à la bioinformatique appliquée à l'analyse des données génétiques dans le cadre des maladies génétiques humaines. Cet enseignement fait partie du Master 2 de Pathologie Humaine dispensé à la faculté de Médecine de la Timone à Marseille.\n \n", "homepage": "http://formations.univ-amu.fr/ME5APH-ENAPHCU41.html", "is_draft": false, "costs": [], "topics": [], "keywords": [ "NGS Data Analysis", "Bioinformatics & Biomedical", "Sequence analysis", "NGS Sequencing Data Analysis" ], "prerequisites": [ "Master (M2 uniquement)" ], "openTo": "Internal personnel", "accessConditions": "Inscription au Master 2 de Pathologie Humaine\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/269/?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": 17, "name": "Formation universitaire", "shortName": "", "description": "LABGeM's researchers are involved in different training programs in collaboration with :\nthe University of Paris Saclay: master GENIOMHE, master MSSB, master NRBCe\nthe University Denis Diderot: master M2BI\nthe University Paris Descartes: master IMVI\nthe Institut Pasteur: Training ‘Analyse des génomes’\n", "homepage": "https://labgem.genoscope.cns.fr/professional-trainings/university-trainings/", "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": 393, "name": "Pandas : gérer, analyser, visualiser vos données efficacement", "shortName": "", "description": "Les objectifs de cette formation sont :\r\n- Importer, exporter, gérer, analyser des données tabulaires\r\n- Calculer des données dérivées\r\n- Combiner et interroger des données complexes\r\n- Calculer des statistiques descriptives des données\r\n- Visualiser et synthétiser les données sous formes graphiques", "homepage": "https://cnrsformation.cnrs.fr/python-et-module-pandas-pour-gerer-et-analyser-donnees?mc=Pandas", "is_draft": false, "costs": [ "Priced" ], "topics": [ "http://edamontology.org/topic_0091" ], "keywords": [ "Python Language" ], "prerequisites": [ "Linux - Basic Knowledge" ], "openTo": "Everyone", "accessConditions": "- Notions de base en informatique : fichiers, répertoire, organisation des données\r\n- Connaissance de base de la programmation en Python (activité régulière d'écriture de scripts en Python)\r\n- Maitrise d'un environnement de développement ou éditeur de programmes/scripts", "maxParticipants": 12, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/528/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [ { "id": 6, "name": "CNRS formation entreprise", "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/CNRS%20formation%20entreprise/?format=api" } ], "organisedByOrganisations": [], "organisedByTeams": [ { "id": 7, "name": "ATGC", "url": "https://catalogue.france-bioinformatique.fr/api/team/ATGC/?format=api" } ], "logo_url": "http://www.atgc-montpellier.fr/pictures/ATGClogo.svg", "updated_at": "2025-02-11T08:32:41.454179Z", "audienceTypes": [ "Professional (continued)" ], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "Jour 1\r\nMatin :\r\n- Initiation Pandas, structures de données Series et DataFrame, chargement de données à partir de fichiers de données tabulaires\r\nAprès-midi :\r\n- Requêtes et outils de sélection\r\n\r\nJour 2\r\nMatin :\r\n- Fusion, concaténation, jointure de tables, regroupement de sous-ensembles\r\nAprès-midi :\r\n- Indexation simple et multiple, réindexation, export et sauvegarde\r\n\r\nJour 3\r\nMatin :\r\n- Visualisation et réalisation de graphiques\r\nAprès-midi :\r\n- Analyse de données des participants", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": 21, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/702/?format=api" ] }, { "id": 48, "name": "Analyses bioinformatique et statistiques de données ChIP-seq sous Unix", "shortName": "", "description": "", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "NGS Data Analysis" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "Formations payantes\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": 344, "name": "Analyses Single Cell RNA-seq (ScRNA-seq) avec R", "shortName": "", "description": "Cette formation introduira notamment la librairie Seurat permettant la manipulation et l'analyse de données Single Cell RNA-seq ainsi que la visualisation des résultats d'analyse\r\n\r\n- Rappels des concepts du séquençage Single Cell RNA-seq\r\n- Importation des données Single Cell dans R\r\n- Intégration de données Single Cell multiples\r\n- Quality Check et pré-traitement des données\r\n- Normalisation de données\r\n- Identification de marqueurs\r\n- Clustering et assignation cellulaire\r\n- Analyse différentielle des groupes cellulaires\r\n- Savoir intégrer les données de spatialisation\r\n- Savoir intégrer les données de trajectoire\r\n- Savoir intégrer les données de communication cellulaire\r\n- Savoir intégrer les données d'épigénétique (ATAC-seq)", "homepage": "https://cnrsformation.cnrs.fr/analyses-single-cell-rna-seq-scrna-seq-avec-r?axe=176", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Bioinformatics & Biomedical", "R Language", "R", "NGS Sequencing Data Analysis" ], "prerequisites": [ "Basic knowledge of R", "R programming" ], "openTo": "Everyone", "accessConditions": "Maîtrise du langage R\r\nAvoir suivi le stage \"Langage R : introduction\" ou niveau équivalent.\r\nAfin de vérifier que votre maîtrise du langage R est suffisante pour pouvoir suivre ce stage, nous vous invitons à effectuer et à renvoyer le test téléchargeable\r\nhttps://cnrsformation.cnrs.fr/data/STG_23294_55153.docx", "maxParticipants": 12, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/154/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [ { "id": 6, "name": "CNRS formation entreprise", "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/CNRS%20formation%20entreprise/?format=api" } ], "organisedByOrganisations": [ { "id": 1, "name": "CNRS formation entreprises", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/CNRS%20formation%20entreprises/?format=api" } ], "organisedByTeams": [ { "id": 6, "name": "CBiB", "url": "https://catalogue.france-bioinformatique.fr/api/team/CBiB/?format=api" } ], "logo_url": "https://services.cbib.u-bordeaux.fr/utils/logo_cbib.png", "updated_at": "2023-08-31T09:19:56.754683Z", "audienceTypes": [ "Graduate", "Professional (initial)" ], "audienceRoles": [ "Biologists", "Bioinformaticians" ], "difficultyLevel": "Intermediate", "trainingMaterials": [], "learningOutcomes": "- Savoir expertiser et manipuler des données issues d'expériences Single Cell RNA-seq\r\n- Savoir mener une analyse différentielle à de multiples niveaux\r\n- Savoir intégrer des données complémentaires pour l'analyse Single Cell RNA-seq (spatial, trajectoire, cell communication, cell identification...)", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/650/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/653/?format=api" ] }, { "id": 153, "name": "Cycle « Initiation à la bioinformatique » - Module 1/4 : Banques de données et Blast", "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 1 sont :\r\n- Découvrir différentes banques de données de séquences généralistes\r\n- Savoir interroger les banques de données et réaliser des requêtes pertinentes\r\n- Comprendre la structure des données\r\n- Savoir utiliser de manière optimale le logiciel Blast en fonction de l'application visée (ex : recherche d’homologie, prédiction de gènes…)\r\n- Etre capable d'analyser un résultat avec un regard critique", "homepage": "https://bilille.univ-lille.fr/training/training-offer", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Autre", "Sequence analysis", "Multiple sequence alignment", "Databases and information systems" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "Savoir utiliser un ordinateur (Windows...) : naviguer sur internet (Internet Explorer ou Firefox), utiliser un traitement de texte (Word ou OpenOffice).", "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": "2024-12-09T17:42:24.618464Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [] }, { "id": 2, "name": "Ateliers NGS, Master BIBS U-Psud", "shortName": "", "description": "NA\n", "homepage": "http://www.bibs.u-psud.fr/m2_ami2b.php", "is_draft": false, "costs": [], "topics": [], "keywords": [ "NGS Data Analysis", "Analysis of RNAseq data", "Linux", "Sequence Algorithm", "Gene expression differential analysis", "Transcript and transcript variant analysis", "Transcriptomics (RNA-seq)", "NGS Sequencing Data Analysis" ], "prerequisites": [ "Master" ], "openTo": "Internal personnel", "accessConditions": "BIBS\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": 334, "name": "Summer School Multi-omics Data Analysis and Integration", "shortName": "", "description": "Researchers often have access to or generate multiple omics data (RNAseq, metabolomics, lipidomics, proteomics…) within a single study. 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We will harness this subject introducing semantic web and knowledge graphs in the context of metabolic networks.\r\n\r\nDuring the School, significant time will be devoted to hands-on and the program will be divided into three phases / topics:\r\n- Multivariate statistical analyses (Instructors: Arnaud Gloaguen & Jimmy Vandel)\r\n- Network-based approaches (Instructors: Morgane Térézol & Marie-Galadriel Brière)\r\n- Results contextualisation: an introduction to metabolic models, web semantic and knowledge graphs (Instructors: Jean-Clément Gallardo, Maxime Delmas & Marco Pagni)\r\n\r\nThe participants will work in groups and shortly present the application of what they have learned to their own project.", "homepage": "https://www.sib.swiss/training/course/20230903_MODAI", "is_draft": false, "costs": [], "topics": [ "http://edamontology.org/topic_0089", "http://edamontology.org/topic_2269", "http://edamontology.org/topic_0602" ], "keywords": [ "Biological network inference and analysis", "Multivariate analyses", "Semantic web", "Knowledge representation" ], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": null, "contacts": [], "elixirPlatforms": [ { "id": 1, "name": "Training", "url": "https://catalogue.france-bioinformatique.fr/api/elixirplatform/Training/?format=api" } ], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 100, "name": "SIB", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/SIB/?format=api" }, { "id": 4, "name": "IFB - ELIXIR-FR", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/IFB%20-%20ELIXIR-FR/?format=api" } ], "organisedByTeams": [], "logo_url": null, "updated_at": "2023-04-26T16:14:06.237852Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "Intermediate", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/532/?format=api" ] }, { "id": 125, "name": "Cluster ", "shortName": "", "description": "", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Programming Languages & Computer Sciences", "Autres langages" ], "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": 124, "name": "Intégration d’outils dans la plateforme web GALAXY ", "shortName": "", "description": "", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Galaxy" ], "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": 256, "name": "RNASeq analyses (using Galaxy and TOGGLe)", "shortName": "", "description": "This course offers an introduction to RNASeq analyses using two different workflow management systems: Galaxy and TOGGLe. This includes reference-based mapping, estimates of transcript levels, differential expression (DE) analyses, visualization of statistics results.\r\nPrerequisites\r\nWorkflow management system (Galaxy, TOGGLe)\r\n\r\nProgram\r\nMapping of RNASeq against a transcriptome reference with kallisto (Galaxy)\r\nMapping of RNASeq against an annotated genome reference with TopHat (TOGGLe)\r\nDifferential expression analysis using EdgeR and DESeq2\r\nPlots, clustering, co-expression network: degust, WGCNA\r\n\r\n\r\nLearning objectives\r\nManipulate packages/tools available for searching DE genes\r\nThink about different normalisation methods\r\nDetect differentially expressed genes\r\nCompare results between two approaches\r\n\r\n\r\nInstructors\r\nAlexis Dereeper - alexis.dereeper@ird.fr\r\nSebastien Cunnac - sebastien.cunnac@ird.fr\r\nSebastien Ravel - sebastien.ravel@cirad.fr\r\nChristine Tranchant - christine.tranchant@ird.fr", "homepage": "https://southgreenplatform.github.io/trainings//rnaseq/", "is_draft": false, "costs": [ "Free" ], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "Open to South Green close collaborators", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [ { "id": 24, "name": "South Green", "url": "https://catalogue.france-bioinformatique.fr/api/team/South%20Green/?format=api" } ], "logo_url": "https://southgreenplatform.github.io/trainings//images/southgreenlong.png", "updated_at": "2023-01-24T10:26:00.180547Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/388/?format=api" ] }, { "id": 31, "name": "Fouille de texte", "shortName": "", "description": "http://migale.jouy.inra.fr/?q=fr/formations\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Autre" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "http://migale.jouy.inra.fr/?q=fr/formations\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": 75, "name": "Galaxy: metagenomic: sequence analysis of amplicons from MiSeq and 454 sequencing with FROGS with Galaxy first step and statistics", "shortName": "", "description": "This training session, organized by Bioinfo Genotoul, Sigenae, NED (GenPhySE) and TWB, is designed to help you to deal with NGS data of 16S, 18S ... 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