Training List
Handles creating, reading and updating training events.
GET /api/training/?format=api&offset=20&ordering=maxParticipants
{ "count": 378, "next": "https://catalogue.france-bioinformatique.fr/api/training/?format=api&limit=20&offset=40&ordering=maxParticipants", "previous": "https://catalogue.france-bioinformatique.fr/api/training/?format=api&limit=20&ordering=maxParticipants", "results": [ { "id": 358, "name": "Traitement bioinformatique et analyse différentielle de données d’expression RNA-seq sous Galaxy", "shortName": "Analyse données RNA-seq sous Galaxy", "description": "Objectifs pédagogiques\r\nA l’issue de cette formation, vous serez capable, dans le cadre d’une analyse de données RNA- seq avec génome de référence et plan d’expérience simple :\r\n* de connaître le vocabulaire et les concepts bioinformatiques et biostatistiques ;\r\n* de savoir enchaîner de façon pertinente un ensemble d’outils bioinformatiques et biostatistiques dans l’environnement Galaxy ;\r\n* de comprendre le matériel et méthodes d’un article du domaine ;\r\n* d’évaluer la pertinence d’une analyse RNA-seq en identifiant les éléments clefs et comprendre les particularités liées à la nature des données.\r\n\r\nProgramme\r\nBioinformatique :\r\n* Obtenir des données de qualité : nettoyage, filtrage, qualité\r\n* Aligner les lectures sur un génome de référence\r\n* Détecter de nouveaux transcrits\r\n* Quantifier l’expression des gènes\r\n* Préparer et déployer unensemble d’analyses sur plusieurs échantillons\r\n\r\nBiostatistique :\r\n* Construire un plan d’expérience simple\r\n* Normaliser les données de comptage\r\n* Identifier les gènes différentiellements exprimés\r\n* Se sensibiliser aux tests multiples\r\n\r\nAnalyse de protocoles Bioinformatique et Biostatistiques issus de la littérature", "homepage": "https://documents.migale.inrae.fr/trainings.html", "is_draft": false, "costs": [ "Priced" ], "topics": [ "http://edamontology.org/topic_3308", "http://edamontology.org/topic_0203", "http://edamontology.org/topic_0102", "http://edamontology.org/topic_3170" ], "keywords": [ "Gene expression differential analysis", "RNA-seq", "Transcriptomics" ], "prerequisites": [ "Galaxy - Basic usage" ], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 10, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/769/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 88, "name": "BioinfOmics", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/BioinfOmics/?format=api" }, { "id": 82, "name": "INRAE", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INRAE/?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": "2025-01-23T15:20:05.977558Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "A l’issue de cette formation, vous serez capable, dans le cadre d’une analyse de données RNA- seq avec génome de référence et plan d’expérience simple :\r\n\r\n* de connaître le vocabulaire et les concepts bioinformatiques et biostatistiques ;\r\n* de savoir enchaîner de façon pertinente un ensemble d’outils bioinformatiques et biostatistiques dans l’environnement Galaxy ;\r\n* de comprendre le matériel et méthodes d’un article du domaine ;\r\n* d’évaluer la pertinence d’une analyse RNA-seq en identifiant les éléments clefs et comprendre les particularités liées à la nature des données.", "hoursPresentations": 6, "hoursHandsOn": 12, "hoursTotal": 18, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/583/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/690/?format=api" ] }, { "id": 316, "name": "IMGT® standards, databases, tools and web resources", "shortName": "IMGT workshop", "description": "Presentation of IMGT® patterns and resources for the study of genes, expressed repertoires and three-dimensional structures of immunoglobulins (antibodies) and T cell receptors.", "homepage": "https://www.imgt.org/", "is_draft": false, "costs": [], "topics": [ "http://edamontology.org/topic_3930", "http://edamontology.org/topic_3948" ], "keywords": [ "Protein structures", "Immune repertoire analysis", "Monoclonal antibody", "Immunology" ], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 10, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/339/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": null, "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [ "Researchers", "Biologists", "Bioinformaticians" ], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": 6, "personalised": true, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/485/?format=api" ] }, { "id": 351, "name": "Introduction au language R / Introduction to R langage", "shortName": "Introduction to R langage", "description": "Objectifs pédagogiques :\r\nÀ l’issue de la formation, les stagiaires connaîtront les principales fonctionnalités du langage R et ses principes. Ils seront capables de les appliquer pour effectuer des calculs ou des représentations graphiques simples. Ils seront de plus autonomes pour manipuler leurs tableaux de données.\r\nAttention : ce module n’est ni un module de statistique, ni un module d’analyse statistique des données.\r\n\r\nProgramme :\r\n* Structures et manipulation de données\r\n* Principaux éléments du langage de programmation (boucle, fonctions…)\r\n* Différentes représentations graphiques de données/résultats (plot, histogramme, boxplot)", "homepage": "https://documents.migale.inrae.fr/trainings.html", "is_draft": false, "costs": [ "Priced" ], "topics": [ "http://edamontology.org/topic_0605" ], "keywords": [ "R Language" ], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 10, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/769/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 88, "name": "BioinfOmics", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/BioinfOmics/?format=api" }, { "id": 82, "name": "INRAE", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INRAE/?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": "2024-01-18T12:51:01.486572Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": 2, "hoursHandsOn": 10, "hoursTotal": 12, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/570/?format=api" ] }, { "id": 354, "name": "Introduction aux bonnes pratiques pour des analyses reproductibles", "shortName": "Good practices for better reproducibility of analyses", "description": "Objectifs pédagogiques\r\n\r\nL’objectif de cette formation est d’initier les apprenants aux bonnes pratiques pour la reproductibilité des analyses. Ils apprendront à rédiger des rapports d’analyse en R Markdown et à les déposer sur un dépôt GitHub. Les principes FAIR (faciles à trouver, accessibles, interopérables et réutilisables) et les bases de la rédaction de PGD (plans de gestion de données) seront également présentés. Durant la formation, nous utiliserons RStudio et GitHub.\r\n\r\nProgramme\r\n\r\nPrincipes et enjeux de la recherche reproductible\r\nUtilisation de GitHub\r\nGestion des versions d’un document\r\nRédaction de document computationnel\r\nPartage d’un rapport avec ses collaborateurs\r\nPrincipes FAIR et PGD", "homepage": "https://documents.migale.inrae.fr/trainings.html", "is_draft": false, "costs": [ "Priced" ], "topics": [ "http://edamontology.org/topic_0605" ], "keywords": [ "Reproducibility" ], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 10, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/769/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 88, "name": "BioinfOmics", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/BioinfOmics/?format=api" }, { "id": 82, "name": "INRAE", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INRAE/?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": "2024-01-18T13:15:23.269149Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "L’objectif de cette formation est d’initier les apprenants aux bonnes pratiques pour la reproductibilité des analyses. Ils apprendront à rédiger des rapports d’analyse en R Markdown et à les déposer sur un dépôt GitHub. Les principes FAIR (faciles à trouver, accessibles, interopérables et réutilisables) et les bases de la rédaction de PGD (plans de gestion de données) seront également présentés. Durant la formation, nous utiliserons RStudio et GitHub.", "hoursPresentations": 2, "hoursHandsOn": 4, "hoursTotal": 6, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/573/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/693/?format=api" ] }, { "id": 284, "name": "Analyse primaire de données issues de séquenceurs nouvelle génération sous Galaxy", "shortName": "Analyse de données NGS sous Galaxy", "description": "Objectifs pédagogiques\r\nConnaître les concepts et méthodes bioinformatiques utilisés pour l’analyse primaire de données issues de séquenceurs nouvelle génération (NGS). Savoir effectuer un alignement sur un génome de référence, un assemblage de novo d’un génome bactérien\r\n\r\nProgramme\r\nThéorie\r\n* Présentation des différents types de technologies de séquençage (lectures longues et courtes)\r\n\r\nPratique : Analyse des données de séquençage d’un génome bactérien\r\n* Contrôle qualité\r\n* Assemblage de-novo\r\n* Nettoyage des données\r\n* Assemblage\r\n* Visualisation et statistiques sur l’assemblage\r\n* Alignement de lectures sur un génome de référence et visualisation\r\nTous les TPs seront réalisés sous l’environnement d’exécution de traitements Galaxy.", "homepage": "https://documents.migale.inrae.fr/trainings.html", "is_draft": false, "costs": [ "Priced" ], "topics": [ "http://edamontology.org/topic_0092", "http://edamontology.org/topic_0102", "http://edamontology.org/topic_0196", "http://edamontology.org/topic_3168" ], "keywords": [ "Galaxy", "NGS" ], "prerequisites": [ "Galaxy - Basic usage" ], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 10, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/769/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 88, "name": "BioinfOmics", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/BioinfOmics/?format=api" }, { "id": 82, "name": "INRAE", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INRAE/?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": "2024-01-18T13:51:11.796060Z", "audienceTypes": [ "Professional (continued)" ], "audienceRoles": [ "All" ], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "Connaître les concepts et méthodes bioinformatiques utilisés pour l’analyse primaire de données issues de séquenceurs nouvelle génération (NGS). Savoir effectuer un alignement sur un génome de référence, un assemblage de novo d’un génome bactérien", "hoursPresentations": 3, "hoursHandsOn": 3, "hoursTotal": 6, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/582/?format=api" ] }, { "id": 361, "name": "Initiation à Linux / Introduction to Linux", "shortName": "Initiation à Linux", "description": "Objectifs pédagogiques\r\nÀ l'issue de la formation, les stagiaires connaîtront les principales commandes Linux et sauront utiliser le système Linux.\r\n\r\nProgramme\r\n* Connexion (ssh) et transferts de fichiers (scp, rsync)\r\n* Interfaces graphiques (Gnome, KDE) / émulateurs\r\n* Aide en ligne\r\n* Utilisation du shell : le rappel des commandes, l’historique, la complétion\r\n* Système de fichiers : arborescence et chemin d’accès, le répertoire d’accueil…\r\n* Gestion des fichiers et des répertoires\r\n* Principe de protection : les attributs sur les fichiers, les droits d’accès", "homepage": "https://documents.migale.inrae.fr/trainings.html", "is_draft": false, "costs": [ "Priced" ], "topics": [ "http://edamontology.org/topic_0605" ], "keywords": [ "Linux" ], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 10, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/769/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 88, "name": "BioinfOmics", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/BioinfOmics/?format=api" }, { "id": 82, "name": "INRAE", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INRAE/?format=api" } ], "organisedByTeams": [ { "id": 10, "name": "MIGALE", "url": "https://catalogue.france-bioinformatique.fr/api/team/MIGALE/?format=api" } ], "logo_url": "https://migale.inrae.fr/sites/default/files/migale-orange_0.png", "updated_at": "2024-01-18T14:43:04.391836Z", "audienceTypes": [ "Professional (continued)" ], "audienceRoles": [ "Biologists" ], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "À l'issue de la formation, les stagiaires connaîtront les principales commandes Linux et sauront utiliser le système Linux.", "hoursPresentations": 1, "hoursHandsOn": 5, "hoursTotal": 6, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/586/?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_0102", "http://edamontology.org/topic_2885" ], "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/634/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/530/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/724/?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": 63, "name": "Cluster", "shortName": "", "description": "This training session is designed to help you deal with the platform compute cluster and data banks. You will launch your first processing batch on the cluster and will learn how to track and manage them. Organized jointly by the Sigenae and bioinfo genotoul platforms.", "homepage": "http://bioinfo.genotoul.fr/index.php/events/cluster-2/", "is_draft": false, "costs": [ "Priced", "Non-academic: 550€ + 20% taxes (TVA)", "Academic but non-INRAE: 170 € + 20% taxes (TVA)", "For INRAE's staff: 150 € no VAT charged;" ], "topics": [], "keywords": [ "Linux", "Cluster" ], "prerequisites": [ "Linux/Unix" ], "openTo": "Everyone", "accessConditions": "You need to register (via the website) and pay 170 euros a day for academic and 550 euros a day for a private.", "maxParticipants": 12, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/344/?format=api" ], "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": "http://bioinfo.genotoul.fr/wp-content/uploads/bioinfo_logo-rvb-petit.png", "updated_at": "2025-12-01T11:56:37.014694Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "Novice", "trainingMaterials": [ { "id": 139, "name": "Cluster Slides", "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/Cluster%20Slides/?format=api" }, { "id": 140, "name": "TP Cluster", "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/TP%20Cluster/?format=api" } ], "learningOutcomes": "", "hoursPresentations": 3, "hoursHandsOn": 3, "hoursTotal": 6, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/475/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/477/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/610/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/261/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/633/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/668/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/529/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/720/?format=api" ] }, { "id": 289, "name": "Introduction to galaxy: looking for variants in prokaryotes", "shortName": "Introduction to galaxy", "description": "This course will focus on the technical aspects of using a galaxy server. Accessible without any prerequisite in computer science, it will allow you to master the different fundamental tools of galaxy and will open the doors of bioinformatics analysis for your different projects.\r\nDifferent questions will be addressed through an example of variants analysis in a prokaryotic organism. At the end of this course, on any accessible galaxy instance, you will be able to:\r\n- upload your data\r\n- map them on a reference genome\r\n- find the variants (SNPs) and analyze the results\r\n- generate, manipulate and share your workflows, data and histories\r\n- find the right tools for other analyses and use them in your own project.\r\n\r\nUnless all participants speak French, the course will be taught in English.", "homepage": "https://pliniuscursus.univ-amu.fr/formation/galaxy-platform/", "is_draft": false, "costs": [ "Free to academics" ], "topics": [ "http://edamontology.org/topic_0091", "http://edamontology.org/topic_0622" ], "keywords": [], "prerequisites": [ "Master" ], "openTo": "Internal personnel", "accessConditions": "The first sessions are only available for IM2B students.", "maxParticipants": 12, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "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": 315, "name": "Using sed and awk to modify large large text files", "shortName": "", "description": "Many analysis generate large result text files which have to be checked, merged, split, reduced. Several tools have been developed and are available on Unix to do this, including sed and AWK. During this course you will be trained to process large files with sed and AWK. Sed is tool enabling to select and process lines. You can easily insert, delete, modify, append lines to very large files with millions of lines. AWK will enable to perform more fine tuned file modifications based on columns. It includes also more mathematical and string functions. The course is based mainly on exercises with small sections presenting concepts and commands.", "homepage": "http://bioinfo.genotoul.fr/index.php/events/modify-and-extract-information-from-large-text-files-day-2-3/", "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_3316" ], "keywords": [], "prerequisites": [ "Linux/Unix" ], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 12, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/338/?format=api" ], "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": "http://bioinfo.genotoul.fr/wp-content/uploads/bioinfo_logo-rvb-petit.png", "updated_at": "2025-12-01T11:57:16.182121Z", "audienceTypes": [ "Professional (continued)" ], "audienceRoles": [ "Biologists" ], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": false, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/478/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/479/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/611/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/631/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/669/?format=api" ] }, { "id": 375, "name": "RNASeq Analysis", "shortName": "RNASeq Analysis", "description": "Objectives\r\n- Understand the key steps in RNASeq data analysis for a differential expression study\r\n- Know how to perform command-line analysis using Snakemake.\r\n\r\nPedagogical Content\r\nDay 1\r\n- Principle of RNASeq technology: objectives and experimental design.\r\n- Data quality assessment (FastQC, MultiQC).\r\n- Sequence alignment to a reference genome (STAR).\r\n\r\nDay 2\r\n- Differential gene expression analysis (HTSeqCount, DESeq2).\r\n- Functional annotation (GO, Kegg).\r\n- Using the Snakemake workflow system.\r\n- Comparison between RNASeq and 3’SRP methods.\r\n\r\nThe theoretical part is followed by a pipeline run step-by-step on a test dataset. \r\nIt will be possible to start an analysis on your own data.", "homepage": "https://pf-bird.univ-nantes.fr/training/rnaseq/", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Everyone", "accessConditions": "Familiarity with basic Linux commands.", "maxParticipants": 12, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [ { "id": 16, "name": "BiRD", "url": "https://catalogue.france-bioinformatique.fr/api/team/BiRD/?format=api" } ], "logo_url": null, "updated_at": "2024-02-08T16:07:26.347245Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": 7, "hoursHandsOn": 7, "hoursTotal": 14, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/603/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/640/?format=api" ] }, { "id": 290, "name": "NGS data analysis on the command line", "shortName": "NGS-analysis-cli", "description": "This hands-on course will teach bioinformatic approaches for analyzing Illumina sequencing data. Our goal is to introduce the command line skills you need to make the most of your NGS data. \r\nDuring this 4-day training we will first introduce the Linux environment, shell commands and basic R scripting. And then we will focus on two NGS data analyses -- small RNA-seq and RNA-seq -- based on published datasets from the model organism Arabidopsis thaliana", "homepage": "https://www.ibmp.cnrs.fr/bioinformatics-trainings/", "is_draft": false, "costs": [ "Free to academics" ], "topics": [ "http://edamontology.org/topic_0102", "http://edamontology.org/topic_3170", "http://edamontology.org/topic_2269", "http://edamontology.org/topic_3168" ], "keywords": [], "prerequisites": [ "none" ], "openTo": "Internal personnel", "accessConditions": "This training is dedicated to academics working in a laboratory of Unistra/CNRS.", "maxParticipants": 12, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/124/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 79, "name": "IBMP", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/IBMP/?format=api" } ], "organisedByTeams": [ { "id": 14, "name": "BiGEst", "url": "https://catalogue.france-bioinformatique.fr/api/team/BiGEst/?format=api" } ], "logo_url": null, "updated_at": "2024-01-22T14:51:37.215331Z", "audienceTypes": [], "audienceRoles": [ "Biologists", "Bioinformaticians" ], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "Applied Knowledge (Know-how):\r\n- Basic proficiency at the Linux command line prompt\r\n- Basic proficiency of R (environment, objects, graphs) \r\n- Next generation sequencing (NGS) file formats; reference genomes - Mapping NGS read data to reference genomes (bowtie, samtools)\r\n- Small RNA-seq analysis; epigenomics applications (ShortStack)\r\n- RNA-seq for transcriptomics; differential gene expression analysis (HISAT2, DESeq2) - Data wrangling and visualization in R (Rstudio, ggplot2)", "hoursPresentations": 12, "hoursHandsOn": 16, "hoursTotal": 28, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/503/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/504/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/589/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/454/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/660/?format=api" ] }, { "id": 380, "name": "INTRODUCTION TO PYTHON", "shortName": "Python", "description": "The Toulouse Genotoul bioinformatics platform, organizes a 2 days long training course for non computer scientist and biologists aiming at learning the foundation of Python programming. In this training you will learn the basics of programming (variables, functions, control structures such as “if” condition, “for” loop”), writing simple programs which read files, and write results to others. The training course does not require any knowledge in programming, but basic Linux/bash commands are required (cd, ls).\r\n\r\nThis training focuses on practice. It consists of modules with a large variety of exercises described hereunder (PROVISIONAL SCHEDULE):\r\n\r\nUsing a Jupyter notebook (Day 1).\r\nUsing variables (Day 1).\r\nBasic operations and functions (Day 1).\r\nReading a file, writing to a file (Day 1).\r\nCharacter string manipulation (Day 1).\r\nLists and dictionaries (Day 2).\r\nThe if and for controls (Day 2).\r\nBases of algorithms (Day 2).", "homepage": "https://bioinfo.genotoul.fr/index.php/events/python/", "is_draft": false, "costs": [], "topics": [ "http://edamontology.org/topic_3307" ], "keywords": [ "Python Language" ], "prerequisites": [ "Linux/Unix" ], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 12, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/642/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 15, "name": "MIAT", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/MIAT/?format=api" } ], "organisedByTeams": [ { "id": 22, "name": "Genotoul-bioinfo", "url": "https://catalogue.france-bioinformatique.fr/api/team/Genotoul-bioinfo/?format=api" } ], "logo_url": "http://bioinfo.genotoul.fr/wp-content/uploads/bioinfo_logo-rvb-petit.png", "updated_at": "2025-12-01T11:55:51.057828Z", "audienceTypes": [ "Professional (continued)" ], "audienceRoles": [ "Life scientists" ], "difficultyLevel": "Novice", "trainingMaterials": [ { "id": 142, "name": "Introduction to python", "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/Introduction%20to%20python/?format=api" } ], "learningOutcomes": "", "hoursPresentations": 5, "hoursHandsOn": 9, "hoursTotal": 14, "personalised": false, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/635/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/718/?format=api" ] }, { "id": 381, "name": "HOW TO RUN A NF-CORE NEXTFLOW WORKFLOW ON GENOTOUL ?", "shortName": "Nextflow/nf-core", "description": "This training session is organized by the Genotoul bioinfo platform and aims at learning nf-core workflow submission, error understanding, resuming jobs and ressource reservation. We will present and practice:\r\n\r\nthe Nextflow software\r\nthe nf-core community and pipelines\r\nWhat is a singularity image ?\r\nWhere are installed the nf-core workflows ? Which version do I use ?\r\nHow to run a workflow and which config file is used ?\r\nWhich kind of error I can get ?\r\nHow to resume failed jobs?\r\nHow to handle genome indexes ?\r\nHow to monitor my process and then well configure my workflow ?\r\nHow do you best adjust CPU and RAM reservations?\r\nThis is NOT a bioinformatic training on a particular workflow or a training on how to develop a workflow.\r\n\r\nThis training is focused on practice. It consists of several modules with a large variety of exercises:\r\n\r\nStart at 09:00 am\r\nEnd at 17:00 pm", "homepage": "https://bioinfo.genotoul.fr/index.php/events/how-to-run-a-nf-core-nextflow-workflow-on-genotoul-2/", "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_0769" ], "keywords": [ "Nextflow" ], "prerequisites": [ "Linux/Unix", "Cluster" ], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 12, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/300/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 15, "name": "MIAT", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/MIAT/?format=api" } ], "organisedByTeams": [ { "id": 22, "name": "Genotoul-bioinfo", "url": "https://catalogue.france-bioinformatique.fr/api/team/Genotoul-bioinfo/?format=api" } ], "logo_url": "http://bioinfo.genotoul.fr/wp-content/uploads/bioinfo_logo-rvb-petit.png", "updated_at": "2025-12-01T11:57:33.124156Z", "audienceTypes": [ "Professional (continued)" ], "audienceRoles": [ "Life scientists" ], "difficultyLevel": "Novice", "trainingMaterials": [ { "id": 143, "name": "workflows nf-core", "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/workflows%20nf-core/?format=api" } ], "learningOutcomes": "", "hoursPresentations": 1, "hoursHandsOn": 6, "hoursTotal": 7, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/636/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/722/?format=api" ] }, { "id": 336, "name": "Pipelines et méthodes bioinformatiques pour l'analyse de données de séquençage (NGS)", "shortName": "", "description": "Bilille propose des formations en partenariat avec CNRS Formation Entreprises à destination des chercheur-euse-s, enseignant-e-s-chercheur-euse-s, ingénieur-e-s, technicien-ne-s en biologie et médecine. \r\n\r\nObjectifs :\r\n- Comprendre les principes des méthodes d'analyse de données de séquençage à haut débit (NGS)\r\n- Comprendre les paramètres des méthodes et leur impact sur les résultats\r\n- Apprendre à identifier les outils d'analyse en fonction du jeu de données\r\n- Être autonome pour analyser des données dans un gestionnaire de workflow comme Galaxy\r\n- Savoir manipuler les fichiers de lecture de séquençage : extraction, préparation, filtrage / nettoyage\r\n- Savoir évaluer la qualité des données de séquençage\r\n- Savoir analyser des données de séquençage de génomes (avec ou sans génome de référence) et prendre du recul sur le protocole expérimental\r\n- Savoir analyser des données de RNA-seq (avec ou sans génome de référence) et prendre du recul sur le protocole expérimental", "homepage": "https://cnrsformation.cnrs.fr/pipelines-et-methodes-bioinformatiques-pour-analyse-de-donnees-de-sequencage", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 12, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/487/?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": 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": "2024-12-09T17:40:53.734910Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/541/?format=api" ] }, { "id": 288, "name": "Introduction to Linux", "shortName": "BirdLinux", "description": "Objectives\r\n- Understand the principles and advantages of the Linux system\r\n- Know and use the main bash commands. Ability to chain multiple commands using pipes\r\n- Launch programs with arguments\r\n- Gain independence to perform command line analyses\r\n\r\nPedagogical Content\r\n- Introduction to the Linux system.\r\n- File system: directory structure, paths, home directory, file and directory management.\r\n- Principle of protections: reading file attributes, access rights, management of user groups.\r\n- Shell usage: command reminders, input/output redirection, history, completion, launching programs with arguments.\r\n- Commands relevant to bioinformatics: grep, cut, sed, sort, more, etc.\r\n- Connection (ssh) - how to start a session from Linux or Windows PowerShell", "homepage": "https://pf-bird.univ-nantes.fr/training/", "is_draft": false, "costs": [ "Priced" ], "topics": [ "http://edamontology.org/topic_0605" ], "keywords": [], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 12, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/596/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [ { "id": 16, "name": "BiRD", "url": "https://catalogue.france-bioinformatique.fr/api/team/BiRD/?format=api" } ], "logo_url": "https://pf-bird.univ-nantes.fr/medias/photo/small_1612545616928-png", "updated_at": "2024-02-08T15:29:55.120700Z", "audienceTypes": [ "Professional (continued)" ], "audienceRoles": [ "Biologists", "All" ], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": 1, "hoursHandsOn": 6, "hoursTotal": 7, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/601/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/639/?format=api" ] }, { "id": 306, "name": "Molecular Phylogeny - Level 1", "shortName": "Phylogénie moléculaire - Niveau 1", "description": "OBJECTIF\r\n- Savoir inférer un arbre phylogénétique et l'interpréter\r\n\r\nPRÉREQUIS\r\n- Savoir ce à quoi correspondent des séquences génétiques homologues\r\n- Avoir déjà utilisé les logiciels de base en bioinformatique\r\n- Connaître les notions de base en statistiques (tests, lois probabilistes usuelles, méthodes simples d'estimation de paramètres)\r\n- Avoir des notions de programmation\r\n\r\nPROGRAMME\r\n- Lignes de commandes Linux\r\n- Le format Newick\r\n- Dessin d'arbres\r\n- Alignements multiples et nettoyage\r\n- Modèles d'évolution\r\n- Choix de modèles\r\n- Définitions et propriétés des arbres\r\n- Méthodes de parcimonie\r\n- Méthodes de distance\r\n- Maximum de vraisemblance\r\n- Reconstruction phylogénétique Bayésienne\r\n- Bootstraps et autres supports de branches", "homepage": "", "is_draft": false, "costs": [ "1200 €" ], "topics": [ "http://edamontology.org/topic_0084", "http://edamontology.org/topic_3293", "http://edamontology.org/topic_3299" ], "keywords": [], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 12, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/241/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 1, "name": "CNRS formation entreprises", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/CNRS%20formation%20entreprises/?format=api" } ], "organisedByTeams": [ { "id": 7, "name": "ATGC", "url": "https://catalogue.france-bioinformatique.fr/api/team/ATGC/?format=api" } ], "logo_url": "https://ressources.france-bioinformatique.fr/sites/default/files/ATGClogox120_0.png", "updated_at": "2023-01-24T10:44:55.936489Z", "audienceTypes": [ "Professional (continued)" ], "audienceRoles": [], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "To know how to infer a phylogenetic tree and interpret it.", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": true, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/460/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/509/?format=api" ] }, { "id": 324, "name": "Python scripts for bioinformatics and Linux", "shortName": "Scripts en Python pour la bioinformatique et environnement Linux", "description": "OBJECTIFS\r\n- Connaître les principes et les avantages du système Linux\r\n- Connaître et savoir utiliser les commandes de base permettant de lancer des programmes sous Linux\r\n- Comprendre et savoir lancer des scripts\r\n- Être capable d'écrire des scripts en Python\r\n- Acquérir de l'autonomie pour effectuer des analyses bioinformatiques qui combinent plusieurs outils \r\n\r\nPRÉREQUIS\r\n- Notions de base en informatique : fichiers, répertoires, etc. \r\n\r\nPROGRAMME\r\n- Linux : lignes de commandes, principales commandes, redirection\r\n- Lancer, créer et modifier des scripts\r\n- Notions de variables, de boucles, de choix\r\n- Programmation de scripts : utilisation de paramètres et de variables, combinaison d'outils et de logiciels, écriture des résultats dans un ou plusieurs fichiers\r\n- Création d'un pipeline d'outils", "homepage": "", "is_draft": false, "costs": [ "1200 €" ], "topics": [], "keywords": [ "Linux", "Python Language" ], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "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://www.france-bioinformatique.fr/sites/default/files/ATGClogox120_0.png", "updated_at": "2025-01-23T13:50:29.570608Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/512/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/703/?format=api" ] }, { "id": 279, "name": "Annotation and analysis of prokaryotic genomes using the MicroScope platform", "shortName": "MicroScope training", "description": "In an effort to inform members of the research community about our annotation methods, to provide training for collaborators and other scientists who use the MicroScope platfom, and to inform scientific public on the analysis available in PkGDB (Prokaryotic Genome DataBase), we have developed a 4.5-day course in Microbial Genome Annotation and Comparative Analysis using the MaGe graphical interfaces.\r\n\r\nThis course will familiarize attendees with LABGeM’s annotation pipeline and the manual annotation software MaGe (Magnifying Genome) . No specific bioinformatics skill is required: detailed instruction on the algorithm developed in each annotation methods can be found in specific training courses on «Genomic sequences analysis». Here we focus on the general idea behind each method and, above all, the way you can interpret the corresponding results and combine them with other evidences in order to change or correct the current automatic functional annotation of a given gene, if necessary.\r\n\r\nThis course will also describe how to perform effective searches and analysis of procaryotic data using the graphical functionalities of the MaGe’s interfaces. Because of the numerous pre-computation available in our system (results of “common” annotation tools, synteny with all complete bacterial genomes, metabolic pathway reconstruction, fusion/fission events, genomic islands, …), many practical exercises allow attendees to get familiar with the use the MaGe graphical interfaces in order to efficiently explore these sets of results.", "homepage": "https://labgem.genoscope.cns.fr/professional-trainings/microscope-professional-trainings/training-annotation-analysis-of-prokaryotic-genomes-using-the-microscope-platform/", "is_draft": false, "costs": [ "Priced" ], "topics": [ "http://edamontology.org/topic_0797", "http://edamontology.org/topic_0085", "http://edamontology.org/topic_3301" ], "keywords": [], "prerequisites": [ "Licence" ], "openTo": "Everyone", "accessConditions": "External training sessions can also be scheduled on demand, in France or abroad. See : https://labgem.genoscope.cns.fr/professional-trainings/microscope-professional-trainings/external-microscope-professional-training-sessions/", "maxParticipants": 12, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [ { "id": 15, "name": "Laboratory of Bioinformatics Analyses for Genomics and Metabolism", "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/Laboratory%20of%20Bioinformatics%20Analyses%20for%20Genomics%20and%20Metabolism/?format=api" } ], "organisedByOrganisations": [ { "id": 67, "name": "University Paris-Saclay", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/University%20Paris-Saclay/?format=api" } ], "organisedByTeams": [ { "id": 9, "name": "MicroScope", "url": "https://catalogue.france-bioinformatique.fr/api/team/MicroScope/?format=api" } ], "logo_url": "https://ressources.france-bioinformatique.fr/sites/default/files/plateforme-logo/MicroScope_logo.png", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [ "Undergraduate", "Graduate", "Professional (continued)" ], "audienceRoles": [ "Researchers", "Life scientists", "Biologists", "Curators" ], "difficultyLevel": "Intermediate", "trainingMaterials": [], "learningOutcomes": "Annotation and comparative analysis of bacterial genomes:\r\n\r\n- acquire theoretical and practical knowledge of genome annotation tools (structural and functional annotation, metabolic networks annotation)\r\n- interpret the results of functional annotation tools\r\nperform various comparative analyses : conserved synteny analyses, pan-genome, phylogenetic and metabolic profiles.\r\n- analyse the results of metabolic networks prediction tools and look for candidate genes for enzyme activities.\r\n- use the tools to analyse the genome(s) of interest of participants", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": 31, "personalised": false, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/439/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/506/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/436/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/507/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/577/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/576/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/659/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/658/?format=api" ] } ] }
