Training List
Handles creating, reading and updating training events.
GET /api/training/?format=api&offset=160&ordering=logo_url
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"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/258/?format=api" ] }, { "id": 41, "name": "RNASeq data analysis", "shortName": "", "description": "\nObjectives :\n Understand the main steps in analyzing RNAseq data for a differential gene expression study\n How to perform a command line analysis with Snakemake\nAlternating between theoretical and practical parts.\nPrerequisite: knowledge of command line usage or having followed the \"Introduction to the command line\" training course.\n\n", "homepage": 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Se familiariser avec le système Unix/Linux, la ligne de commande et la gestion et l'analyse de données sur un serveur à distance. Connaître et savoir utiliser les principaux logiciels dédiés à l'analyse de données de séquençage nouvelle génération, de l'alignement des séquences brutes à l'annotation de variations génétiques. Maîtriser les principaux navigateurs, bases de données et outils de prédiction couramment utilisés en génétique humaine et médicale. Connaître les différentes applications possibles du séquençage nouvelle génération pour le diagnostic de maladies génétiques, les principales règles à suivre et paramètres à considérer pour assurer la qualité des données produites dans un contexte de laboratoire médical, et les considérations éthiques que soulève le séquençage nouvelle génération pour l'interprétation et le rendu des résultats.\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [], "prerequisites": [ "Autre (Diplôme universitaire, école d'ingénieur ...)" ], "openTo": "Internal personnel", "accessConditions": "Aucune\n", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [] }, { "id": 194, "name": "NGS et Cancer (Canceropôle) : Analyse DNASeq", "shortName": "", "description": "", "homepage": "", "is_draft": false, "costs": [ "Free" ], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/321/?format=api" ] }, { "id": 195, "name": "NGS et Cancer (Canceropôle) : Analyse A-RNASeq", "shortName": "", "description": "", "homepage": "", "is_draft": false, "costs": [ "Free" ], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/322/?format=api" ] }, { "id": 156, "name": "Python for biology", "shortName": "", "description": "", "homepage": "https://cnrsformation.cnrs.fr/stage-17266-Python-pour-la-biologie.html", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [ "Sequence Algorithm", "Python Language", "Sequence analysis" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "CNRS fee-based training\n", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [] }, { "id": 15, "name": "IFSBM", "shortName": "", "description": "\nUFR médecine Paris-Sud (mai 2015). Big data en médecine. Acquisition et analyse des données de haut débit dans le but de détecter des variants génomiques (CGH, exome, génome), étudier les profils d’expression ou le statut épigénétique des cellules (expression array, RNA-seq, ChiP-seq, medip-seq).\n \nUFR médecine Paris-Sud (janvier 2015) Méthodologie en biologie moléculaire et cellulaire et analyse d’article\n\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [], "prerequisites": [ "Autre (Diplôme universitaire, école d'ingénieur ...)" ], "openTo": "Internal personnel", "accessConditions": "", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [] }, { "id": 251, "name": "Survival Guide for Perl applied to Bioinformatics", "shortName": "", "description": " \n\n\t\t\tThis 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\nPrerequisites\nBasic knowledge of Linux (Linux for dummies required)\n\nProgram\nPerl data structures (scalar,arrays, hashes)\nStructure control ( loops)\nBasic functions, and operators.\nWriting and running your own program\nPassing options and files to his own script.\nRegular expressions\n\n\nLearning objectives\nWriting simple Perl programs to analyze data files\nUnderstanding Perl programs written by others\nUsing Perl basic syntax and modules in their own script\nRun programs from their script, parsing and extracting data from data files\n\n\nInstructors\n\n\nChristine Tranchant - christine.tranchant@ird.fr\nFrançois Sabot - francois.sabot@ird.fr\nNdomassi tando - ndomassi.tando@ird.fr\n\n", "homepage": "https://southgreenplatform.github.io/trainings//perl/", "is_draft": false, "costs": [ "Free" ], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 12, "name": "LAPSE", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/LAPSE/?format=api" }, { "id": 13, "name": "Formation permanente IRD", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/Formation%20permanente%20IRD/?format=api" } ], "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/383/?format=api" ] }, { "id": 127, "name": "Linux avancé", "shortName": "", "description": "", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Programming Languages & Computer Sciences", "Linux" ], "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": 47, "name": "Analyse de données RNA-seq sous l’environnement Galaxy ", "shortName": "", "description": "\n\nObjectifs de la formation\nAcquérir les connaissances générales sur les méthodes de séquençage à haut-débit.\nConnaître les caractéristiques des données obtenues dans le cadre de l’analyse du transcriptome (RNA-seq).\nSavoir planifier une expérience simple de type RNA-seq en fonction de ses objectifs scientifiques et des caractéristiques et contraintes expérimentales.\nConnaître les principales méthodes et outils d’analyse des données RNA-seq . Pouvoir les mettre en oeuvre dans un cas simple via un serveur web Galaxy.\nPouvoir visualiser les résultats dans un navigateur de génome.\nDurée de la formation : 2,5 jours\n\n\n", "homepage": "http://www.biosciencesco.fr/formation-continue/bio-informatique/analyse-des-donn…", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Methodology", "Biostatistics", "NGS Data Analysis", "Analysis of RNAseq data", "Assembly of genomes and transcriptomes", "Read alignment on genomes", "Statistical Tests", "Gene expression differential analysis", "Galaxy", "Transcript and transcript variant analysis", "Transcriptomics (RNA-seq)", "NGS Sequencing Data Analysis" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "Informations et inscriptions:\nhttp://www.biosciencesco.fr/formation-continue/bio-informatique/analyse-...\n", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], 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Découvrir les bonnes pratiques dans Galaxy. 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