Training List
Handles creating, reading and updating training events.
GET /api/training/?format=api&offset=220&ordering=accessConditions
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DNA produced with MiSeq from Illumina and Roche 454 technologies in the Galaxy workbench.\nYou will discover how to use our Galaxy instance, clean reads, clusterize them, do the taxonomic affiliation and perform statistics to interpret your results.\nPrerequisites: knowledge of R or in another programming language\n", "homepage": "http://bioinfo.genotoul.fr/index.php", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Galaxy" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "An account on the platform Bioinfo Genotoul is necessary (request a form on the website), you need to register (via the website) and pay 165 euros a day for academic and 550 euros a day for a private\n", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [] }, { "id": 3, "name": "R Biostats Network", "shortName": "", "description": "The program provides an introduction to biostatistical approaches. The principles, methodologies, uses, and applications of statistical methods in biological and clinical research will be presented. Practical trainings on computer with the R software are planned. The bases of the R programming language will be introduced and statistical approaches presented in the theoretical session will be applied.\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Programming Languages & Computer Sciences" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "Aucun\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": 4, "name": "Introduction to data analysis with R", "shortName": "", "description": "The program includes an introduction:\nApproaches in biostatistics and research, explaining to participants the principles, methodologies, use of statistical methods and applications in biology and clinical research.\nCourses on software R will be delivered in the form of additional exercises. The basis of the programming language R will be discussed and statistical approaches presented in the theoretical part will be implemented.\nApplication of skills acquired over a personal dataset\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Programming Languages & Computer Sciences", "R Language" ], "prerequisites": [], "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": 5, "name": "Partek Workshop", "shortName": "", "description": "Introduction to Partek® software and the principles of RNA-seq data analysis DNA-Seq analysis and annotations with Partek® Genomics Suite® Hands on analysis in Partek® Flow® including: Data import and sample annotation, Pre and post alignment quality control, Gene and transcript quantification, Detection of differential expression using powerful gene specific modeling\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Bioinformatics & Biomedical" ], "prerequisites": [], "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": 6, "name": "Ingenuiy Pathways Analysis Workshop", "shortName": "", "description": "The User Group Meeting will consist of talks, customer case studies and interactive feedback sessions where new and existing users of QIAGEN’s Ingenuity products can learn about product updates, usability tips & tricks and best practices. Take advantage of this opportunity to engage with other users from the scientific community.\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Bioinformatics & Biomedical" ], "prerequisites": [], "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": 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": 7, "name": "InSilicoDb Analysis Training", "shortName": "", "description": "Interrogating public and private gene expression datasets for bio-medical researchers. This workshop will you teach about two subjects: 1- Genomics data management for the lab (efficiently store and make accessible microarray and NGS data), 2- Interrogation of your expression data and comparison and combination of your data with public data.\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Bioinformatics & Biomedical" ], "prerequisites": [], "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": 110, "name": "Galaxy : first step", "shortName": "", "description": " \n\nLe programme de cette introduction à Galaxy est le suivant : présentation de Galaxy, se connecter à l’instance toulousaine, commencer à utiliser certains outils bioinformatiques standards, la gestion des fichiers dans galaxy. Découvrir les bonnes pratiques dans Galaxy. Organisée en collaboration avec la plateforme Bioinfo Genotoul.\n\n\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Galaxy" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "Avoir un compte sur la plateforme Bioinfo Genotoul (demande via un formulaire web sur notre site), s’inscrire (via notre site web) et payer 150 euros la journée pour un académique et 500 euros la journée pour un privé.\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": 302, "name": "Initiation à la ligne de commande", "shortName": "", "description": "L’objectif de cette formation est de se familiariser à l’utilisation de la ligne de commande pour un usage sur un cluster de\r\ncalcul afin d’acquérir les bases pour le traitement de données biologiques.\r\nPrésentation de l’infrastructure du cluster de calcul du Mésocentre Clermont Auvergne.\r\nIntroduction à l’environnement Linux.\r\nInitiation à un langage de scripting avec le shell Bash.\r\nManipulation en ligne de commande de fichiers de données d'origine biologique.\r\nComment se connecter au serveur de calcul.\r\nApprentissage du langage informatique Bash et comment naviguer dans un environnement Linux.\r\nExercices pratiques de saisie de commandes sur un terminal sans interface graphique.\r\nApprentissage de la gestion de fichiers, comment les créer, gérer les droits d’accès, les manipuler et les transférer sur le\r\ncluster de calcul ou les récupérer sur son poste de travail local.", "homepage": "https://mesocentre.uca.fr/", "is_draft": false, "costs": [ "Free to academics" ], "topics": [ "http://edamontology.org/topic_0091", "http://edamontology.org/topic_0605" ], "keywords": [], "prerequisites": [ "Licence" ], "openTo": "Everyone", "accessConditions": "Avoir un compte sur le cluster de calcul du Mésocentre Clermont Auvergne (faire une demande le cas échéant sur le site\r\nhttps://hub.mesocentre.uca.fr)\r\nVENIR AVEC UN ORDINATEUR PORTABLE muni d’une connexion à Eduroam opérationnelle.", "maxParticipants": 10, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/261/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 45, "name": "UMR 454 MEDIS INRA-Université Clermont Auvergne", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/UMR%20454%20MEDIS%20INRA-Universit%C3%A9%20Clermont%20Auvergne/?format=api" } ], "organisedByTeams": [ { "id": 31, "name": "AuBi", "url": "https://catalogue.france-bioinformatique.fr/api/team/AuBi/?format=api" } ], "logo_url": "https://mesocentre.uca.fr/medias/photo/logoaubi-2019minus_1553844844490-jpg?ID_FICHE=41175", "updated_at": "2025-02-17T12:44:35.172676Z", "audienceTypes": [ "Professional (initial)" ], "audienceRoles": [ "Life scientists", "Biologists" ], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": 2, "hoursHandsOn": 3, "hoursTotal": 6, "personalised": false, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/482/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/615/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/707/?format=api" ] }, { "id": 135, "name": "hands-on NGS course", "shortName": "", "description": "The aim of this course is to provide students with theory and practical\ntools to analyze Next Generation Sequencing (NGS) data. The course is\ncomposed of a theory and practice lessons . In the first week theory\nsessions will cover the main kind of HTS analyses (re-sequencing and\nvariant analysis, de-novo sequencing, transcriptomics, ChIP-Seq,\nmetagenomics), in addition to some general bioinformatics tools and\nBiostatistics. The second week is dedicated to practice, in which the\nstudents work with their own data in small groups with a mentor that\nguides them. The practice week is designed so the course is of immediate\nuse to each student. We expect the students to go back to their countries\nwith the necessary knowledge to continue working on their own data.\n", "homepage": "http://c3bi.pasteur.fr", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Methodology", "NGS Data Analysis", "Metagenomics", "Gene expression regulation analysis", "metatranscriptomics", "Chip-Seq", "Variant analysis", "Transcriptomics (RNA-seq)", "Genomics (DNA-seq)", "NGS Sequencing Data Analysis" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "belonging to the Institut Pasteur International Network (RIIP) and the University of Sao Paulo.\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": 136, "name": "LeiSHield training course on Next Generation Sequencing", "shortName": "", "description": "The primary aim of this course was to provide a basic understanding of the Leishmania genome, NGS technology and analysis tools, and to develop a basic pipeline for the students to start working on their data. This first pipeline will help to standardize all analysis done in the consortium and should facilitate a posterior paper publication. This pipeline will evolve\nin the context of a collaboration between the Leishield partners and the C3BI, taking into account the difficulties to analyze and interpret the sequence data generated, and the specific needs of each Consortium node. A future Workshop will be organized in June 2016 to tackle all these questions, and to have a follow-up on the analysis.\n", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [ "NGS Data Analysis" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "belonging to the Leishield consortium.\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": 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": 33, "name": "Analyse statistique RNA-seq sous Galaxy", "shortName": "", "description": "\nObjectifs\n\nSe sensibiliser aux concepts et méthodes statistiques pour l'analyse de données transcriptomiques de type RNA-Seq.\nComprendre le matériel et méthodes (normalisation et tests statistiques) d'un article\ndu domaine.\nComprendre les particularités liées à la nature des données.\n\n \n \nProgramme\n\nPlanification expérimentale des expériences RNA-Seq (identification des biais, répétitions, biais contrôlables).\nNormalisation et analyse différentielle : recherche de \"régions d'intérêt\" différentiellement exprimées (modèle linéaire généralisé).\nPrise en compte de la multiplicité des tests.\nLe cours sera illustré par différents exemples et un jeu de données sera traité à l'aide du package R SARTools (basé sur les packages R DESeq2 et edgeR) dans les environnements Galaxy et RStudio.\n", "homepage": "http://migale.jouy.inra.fr/", "is_draft": false, "costs": [], "topics": [], "keywords": [ "NGS Data Analysis", "Analysis of RNAseq data", "Galaxy" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "Ce cycle est ouvert à l'ensemble des agents de l'INRA et aux extérieurs.\n", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/255/?format=api" ] }, { "id": 25, "name": "Modélisation 3D des protéines", "shortName": "", "description": "\nObjectifs\n\nConnaître les bases de la modélisation moléculaire : modélisation par homologie, arrimage (docking) de ligands, mutations in silico. Une demi-journée dédiée à la modélisation de vos protéines d'intérêts.\n\nProgramme\n\n- Visualiser : Connaître les bases de la visualisation des protéines en 3D avec PYmol.\n- Comprendre : Analyse des structures 3D de protéines (RX ou RMN). Recherche d'homologues avec HHpred, I-Tasser, etc... Modélisation par homologie avec Modeller, Phyre2. Principes et applications.\n- Prédire : Docking de ligands avec Autodock. Prédiction des mutations in silico. Principes et applications.\nL'accent sera mis sur les points forts et les limites des différents outils et la pratique avec de nombreux \"hand- on tutorials\"\nPlus une session dédiée : «bring your own protein».\n", "homepage": "http://migale.jouy.inra.fr/", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Autre", "Protein/protein interaction modelisation", "proteins/peptides and proteins/nucleic acids" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "Ce cycle est ouvert à l'ensemble des agents de l'INRA et aux extérieurs.\n", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/248/?format=api" ] }, { "id": 21, "name": "Annotation de génomes microbiens", "shortName": "", "description": "Modules en prépartion....\n", "homepage": "http://migale.jouy.inra.fr/", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Metagenomics", "Genome analysis", "Structural and functional annotation of genomes", "Genomics (DNA-seq)" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "Ce cycle est ouvert à l'ensemble des agents de l'INRA et aux extérieurs.\n", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/247/?format=api" ] }, { "id": 26, "name": "Initiation à Perl", "shortName": "", "description": "\nObjectifs\n\nInitiation à la programmation.\nIdentifier les possibilités offertes par l’écriture de quelques lignes de code.\nRéalisation de tâches simples d’extraction et de reformatage d’informations issues de fichiers texte.\n \n\n \nProgramme\n\n- Présentation de PERL\n- Variables PERL\n- Structures de contrôle\n- Gestion de fichiers\n- Réalisation de programmes simples\n \nIllustration avec des exercices de manipulation de fichiers de séquences et de fichiers de résultats d’outils bioinformatiques. \n \n", "homepage": "http://migale.jouy.inra.fr/", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Programming Languages & Computer Sciences", "Perl Langage" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "Ce cycle est ouvert à l'ensemble des agents de l'INRA et aux extérieurs.\n", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/249/?format=api" ] }, { "id": 32, "name": "Traitements bioinfo RNA-seq ", "shortName": "", "description": "\nObjectifs\n\nConnaitre les concepts et méthodes bioinformatiques utilisées pour l’analyse de données RNA-Seq eucaryote et procaryote.\n\n \nProgramme\n\nThéorie\nBases biologiques des études d’expression\nSéquençage NGS et RNA-Seq, présentation des différents types de séquenceurs\nMéthodes d’alignements spécifiques au RNA-Seq\nReconstruction de transcrits\nAssemblage de novo de transcriptomes\nQuantification\n \nPratique\nTP sur des données de type euraryote\nContrôle qualité\nNettoyage des données\nAlignement sur un génome de référence et épissage\nVisualisation de l’alignement\nDécouverte de nouveaux transcrits\nObtention d’un tableau de comptage\n \nLien avec d'autres modules \nL'analyse statistique des résultats du type d’analyses bioinformatiques effectuées dans ce module est traitée dans le module 16 [Stats & RNA-seq.\n", "homepage": "http://migale.jouy.inra.fr/", "is_draft": false, "costs": [], "topics": [], "keywords": [ "NGS Data Analysis", "Analysis of RNAseq data", "Galaxy" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "Ce cycle est ouvert à l'ensemble des agents de l'INRA et aux extérieurs.\n", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "", "updated_at": "2022-06-02T11:50:50.812642Z", 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