Training List
Handles creating, reading and updating training events.
GET /api/training/?format=api&offset=180&ordering=-trainingMaterials
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Nous présenterons les étapes bioinformatiques nécessaires pour nettoyer les données brutes et les caractériser d’un point de vue taxonomique. Nous aborderons ensuite les différentes stratégies à employer pour assembler les reads et obtenir des comptages sur des gènes prédits. Enfin nous présenterons quelques outils pour obtenir une annotation fonctionnelle des échantillons. A l’issue des 2 jours de formation, les stagiaires connaîtront le périmètre, les avantages et limites des analyses de données de séquençage shotgun. Ils seront capables d’utiliser les outils présentés sur les jeux de données de la formation. L’ensemble des TP se déroulera sur l’infrastructure de Migale et nécessite une pratique courante de la ligne de commande.\r\n\r\nProgramme\r\n\r\nIntroduction générale sur les données métagénomiques\r\nAssignation taxonomique\r\nNettoyage des données brutes\r\nAssemblage / Binning\r\nPrédiction de gènes procaryotes\r\nAnnotation fonctionnelle\r\nConclusion, limites des méthodes", "homepage": "https://documents.migale.inrae.fr/trainings.html", "is_draft": false, "costs": [ "Priced" ], "topics": [ "http://edamontology.org/topic_3697" ], "keywords": [ "Metagenomics" ], "prerequisites": [ "Linux/Unix", "Cluster" ], "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": "2024-01-18T13:16:49.313752Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "Intermediate", "trainingMaterials": [], "learningOutcomes": "Cette formation est dédiée à l’analyse de données métagénomiques procaryotes de type « shotgun » issues de la technologie de séquençage Illumina. 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L’ensemble des TP se déroulera sur l’infrastructure de Migale et nécessite une pratique courante de la ligne de commande.", "hoursPresentations": 5, "hoursHandsOn": 7, "hoursTotal": 12, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/572/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/694/?format=api" ] }, { "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": 216, "name": "Analyse de données métagénomiques 16S", "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/350/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/345/?format=api" ] }, { "id": 202, "name": "Guide de survie à Perl pour la bioinformatique", "shortName": "", "description": "This course provides an introduction to programming using Perl and at the end of the training, participants could write simple Perl programs to handle biological data and to undertstand more complex Perl programs written by others.\n\t\t\t \n \n \n \n", "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/331/?format=api" ] }, { "id": 266, "name": "Analyse de séquences", "shortName": "", "description": "\n\n\nLes biologistes sont régulièrement confrontés à des gènes (ou des protéines) de fonctions inconnues ou mal annotés. Dans ce contexte, maîtriser quelques techniques basiques d’analyse de séquences peut se révéler d’une aide précieuse. \nL’objectif de cette formation est de présenter, au travers de l’utilisation de sites web spécialisés, quelques grands principes sur l’analyse de séquence. L’ensemble de la formation combine exposés théoriques (fondements méthodologiques des programmes) et applications pratiques (mise en relation des notions théoriques avec les paramètres des programmes et les résultats obtenus) pour permettre une utilisation autonome et critique de quelques logiciels d’analyse des séquences biologiques.\n\n\n\n", "homepage": "https://c3bi.pasteur.fr/training-analyse-de-sequences/", "is_draft": false, "costs": [ "Free" ], "topics": [], "keywords": [ "Sequence analysis", "Comparative genomics" ], "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/398/?format=api" ] }, { "id": 129, "name": "R avancé", "shortName": "", "description": "", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Programming Languages & Computer Sciences", "R Language" ], "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": 195, "name": "NGS et Cancer (Canceropôle) : Analyse A-RNASeq", "shortName": "", "description": "", "homepage": "", "is_draft": false, "costs": [ "Free" ], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/322/?format=api" ] }, { "id": 8, "name": "DU \"séquençage haut débit et maladies génétiques\"", "shortName": "", "description": "Acquérir une formation en séquençage nouvelle génération appliqué aux maladies génétiques mendéliennes,des technologies de séquençage et approches expérimentales possibles aux outils bio-informatiques utilisés pour le traitement des données brutes, l'identification de variations génétiques et l'interprétation des résultats. Se familiariser avec le système Unix/Linux, la ligne de commande et la gestion et l'analyse de données sur un serveur à distance. Connaître et savoir utiliser les principaux logiciels dédiés à l'analyse de données de séquençage nouvelle génération, de l'alignement des séquences brutes à l'annotation de variations génétiques. Maîtriser les principaux navigateurs, bases de données et outils de prédiction couramment utilisés en génétique humaine et médicale. Connaître les différentes applications possibles du séquençage nouvelle génération pour le diagnostic de maladies génétiques, les principales règles à suivre et paramètres à considérer pour assurer la qualité des données produites dans un contexte de laboratoire médical, et les considérations éthiques que soulève le séquençage nouvelle génération pour l'interprétation et le rendu des résultats.\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [], "prerequisites": [ "Autre (Diplôme universitaire, école d'ingénieur ...)" ], "openTo": "Internal personnel", "accessConditions": "Aucune\n", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [] }, { "id": 305, "name": "Initiation à Git / Git Initiation", "shortName": "Git Initiation", "description": "Objectifs\r\n- Savoir définir ce qu’est un outil de gestion de version\r\n- Être capable d’initialiser un entrepôt Git pour un projet\r\n- Être capable de définir quels fichiers inclure/exclure d’un projet\r\n- Savoir enregistrer localement une nouvelle version pour un projet\r\n- Savoir partager des modifications locales avec tous les contributeurs d’un projet\r\n- Savoir gérer des modifications en parallèle en utilisant les branches.\r\n- Connaître les bonnes pratiques pour contribuer à projet tiers\r\nProgramme :\r\n- Présentation des avantages de la gestion de versions (projets individuels & projets collaboratifs)\r\n- Présentation des principes de fonctionnement de Git\r\n- Présentation et mise en œuvre des commandes principales de Git (clone, checkout, add, rm, commit, merge,\r\npush, pull) ; 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