Event List
Handles creating, reading and updating events.
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{ "count": 605, "next": "https://catalogue.france-bioinformatique.fr/api/event/?format=api&limit=20&offset=560&ordering=-contacts", "previous": "https://catalogue.france-bioinformatique.fr/api/event/?format=api&limit=20&offset=520&ordering=-contacts", "results": [ { "id": 542, "name": "Analyse bioinformatique des séquences nucléiques et protéiques - session Juin 2023", "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 méthodes de base à utiliser pour mener une analyse de séquences\r\n- Savoir exploiter les ressources bioinformatiques publiques\r\n- Savoir utiliser les logiciels d'alignement, de recherche d'homologie, d'annotation de gènes et de protéines", "homepage": "https://cnrsformation.cnrs.fr/analyse-bioinformatique-sequences-nucleiques-proteiques?axe=161", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": 10, "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": "2024-12-09T17:37:01.837338Z", "type": "Training course", "start_date": "2023-06-21", "end_date": "2023-06-23", "venue": "", "city": "Lille", "country": "FRANCE", "geographical_range": "", "trainers": [], "trainingMaterials": [], "computingFacilities": [], "realisation_status": "past", "registration_opening": null, "registration_closing": "2023-06-23", "registration_status": "closed", "courseMode": "Onsite" }, { "id": 676, "name": "Initiation à Galaxy - session Février 2024", "shortName": "", "description": "Bilille organise régulièrement des formations d'initiation à l'outil Galaxy d'une journée, destinée aux biologistes et médecins désirant découvrir le traitement bioinformatique de données via une interface conviviale.\r\n\r\nGalaxy est très répandu pour l’analyse de données omiques, telles que données de séquençage ou données de puces à ADN. \r\nC'est l'environnement qui est utilisé lors du cycle de formation “Analyse de données de séquençage à haut-débit”.", "homepage": "https://bilille.univ-lille.fr/training/training-offer", "is_draft": false, "costs": [ "Free" ], "topics": [], "keywords": [ "Galaxy" ], "prerequisites": [], "openTo": "Everyone", "accessConditions": "Ouvert en priorité aux participants du cycle Analyse NGS organisé par Bilille.", "maxParticipants": null, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/763/?format=api", "https://catalogue.france-bioinformatique.fr/api/userprofile/487/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [ { "id": 3, "name": "Bilille", "url": "https://catalogue.france-bioinformatique.fr/api/team/Bilille/?format=api" } ], "logo_url": "https://bilille.univ-lille.fr/fileadmin/_processed_/9/2/csm_logo_bilille_complet_65be9bda8b.png", "updated_at": "2024-12-09T17:34:40.543451Z", "type": "Training course", "start_date": "2024-02-21", "end_date": "2024-02-21", "venue": "", "city": "Villeneuve d'Ascq", "country": "FRANCE", "geographical_range": "", "trainers": [], "trainingMaterials": [], "computingFacilities": [], "realisation_status": "past", "registration_opening": null, "registration_closing": "2024-01-19", "registration_status": "closed", "courseMode": "Onsite" }, { "id": 541, "name": "Pipelines et méthodes bioinformatiques pour l'analyse de données de séquençage (NGS) - session Octobre 2023", "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": "2024-12-09T17:37:10.962175Z", "type": "Training course", "start_date": "2023-10-16", "end_date": "2023-10-20", "venue": "", "city": "Lille", "country": "FRANCE", "geographical_range": "", "trainers": [], "trainingMaterials": [], "computingFacilities": [], "realisation_status": "past", "registration_opening": null, "registration_closing": "2023-10-13", "registration_status": "closed", "courseMode": "Onsite" }, { "id": 540, "name": "Cycle « Analyse de données de séquençage à haut-débit » - Module Analyses RNA-seq (sous Galaxy)- session Octobre 2023", "shortName": "", "description": "Bilille, la plateforme de bioinformatique, biostatistique et bioanalyse de la métropole lilloise, propose chaque année un cycle de formation d'introduction à l'analyse des données de séquençage à haut débit.\r\nCe cycle est composé des modules suivants, à la carte : \r\n- Analyses ADN\r\n- Analyses de variants\r\n- Métagénomique\r\n- Analyses ChIP-seq\r\n- Analyses RNA-seq\r\nLes fiches descriptives sont accessibles sur le site de bilille. Chaque module comprend des présentations générales et des séances pratiques sur ordinateur, avec Galaxy.\r\n\r\nLes objectifs du module Analyses RNA-seq sont :\r\n- Découvrir les fonctionnalités courantes de Galaxy, et savoir les utiliser.\r\n- Savoir réaliser une analyse transcriptomique par RNA-seq avec ou sans (de novo) génome de référence à l’aide du portail Galaxy\r\n- Avoir un regard critique sur la qualité des lectures obtenues par le séquenceur\r\n- Connaître et savoir paramétrer les outils nécessaires à l’analyse\r\n- Savoir réaliser une analyse différentielle de données RNA-seq à partir d’une table de comptage (quantifiant les lectures alignées) à l’aide du portail Galaxy\r\n- Avoir un regard critique sur les résultats d’une analyse différentielle\r\n- Comprendre différentes méthodes de normalisation et les contextes d’utilisation correspondants.", "homepage": "https://bilille.univ-lille.fr/training/training-offer", "is_draft": false, "costs": [ "Free to academics" ], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "La première journée du module permettra aux personnes n’ayant pas suivi le module Analyses ADN du cycle de rattraper les pré-requis nécessaires à la suite de la formation (initiation à Galaxy, nettoyage et qualités des séquences, mapping). Des concepts basiques en statistique (moyenne, variance, p-value) sont nécessaires pour être à l’aise dans la quatrième journée.", "maxParticipants": 15, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/763/?format=api", "https://catalogue.france-bioinformatique.fr/api/userprofile/487/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 52, "name": "CNRS", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/CNRS/?format=api" }, { "id": 56, "name": "INSERM", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INSERM/?format=api" }, { "id": 66, "name": "UDL", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/UDL/?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": "2024-12-09T17:37:20.758462Z", "type": "Training course", "start_date": "2023-10-03", "end_date": "2023-10-06", "venue": "", "city": "Villeneuve d'Ascq", "country": "FRANCE", "geographical_range": "", "trainers": [], "trainingMaterials": [], "computingFacilities": [], "realisation_status": "past", "registration_opening": "2023-06-15", "registration_closing": "2023-07-13", "registration_status": "closed", "courseMode": "Onsite" }, { "id": 550, "name": "Cycle « Analyse de données de séquençage à haut-débit » - Module 6/6 : Analyses RNA-seq, biostatistique - session Septembre 2021", "shortName": "", "description": "Bilille propose chaque année un cycle de formation d'introduction à l'analyse des données de séquençage à haut débit.\r\nCe cycle est composé de 6 modules, à la carte : \r\n- Module 1: Analyses ADN\r\n- Module 2: Analyses de variants\r\n- Module 3 : Métagénomique\r\n- Module 4: ChIP-seq\r\n- Module 5: Analyses RNA-seq, bioinformatique\r\n- Module 6: Analyses RNA-seq, biostatistique\r\nLes fiches descriptives sont accessibles sur le site de Bilille. Chaque module comprend des présentations générales et des séances pratiques sur ordinateur, avec Galaxy.\r\nLes objectifs du module 6 sont :\r\n- Savoir réaliser une analyse différentielle de données RNA-seq à partir d’une table de comptage (quantifiant les lectures alignées) à l’aide du portail Galaxy\r\n- Avoir un regard critique sur les résultats d’une analyse différentielle\r\n- Comprendre différentes méthodes de normalisation et les contextes d’utilisation correspondants", "homepage": "https://bilille.univ-lille.fr/training/training-offer", "is_draft": false, "costs": [ "Free" ], "topics": [], "keywords": [], "prerequisites": [ "Galaxy - Basic usage" ], "openTo": "Internal personnel", "accessConditions": "- Etre familier avec la plate-forme web Galaxy (idéalement avoir suivi la formation bilille « Initiation à Galaxy »)\r\n- Avoir suivi le module «Analyses RNA-seq–partie 1 (bioinformatique)» de ce cycle ou toute autre formation permettant de justifier de connaissances sur les données de séquençage haut débit et la façon d’obtenir une table de comptage", "maxParticipants": null, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/487/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 52, "name": "CNRS", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/CNRS/?format=api" }, { "id": 56, "name": "INSERM", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INSERM/?format=api" }, { "id": 66, "name": "UDL", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/UDL/?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": "2024-12-09T17:35:29.098423Z", "type": "Training course", "start_date": "2021-09-23", "end_date": "2021-09-24", "venue": "", "city": "Lille", "country": "FRANCE", "geographical_range": "", "trainers": [], "trainingMaterials": [], "computingFacilities": [], "realisation_status": "past", "registration_opening": null, "registration_closing": "2021-01-06", "registration_status": "closed", "courseMode": "Onsite" }, { "id": 549, "name": "Cycle « Analyse de données de séquençage à haut-débit » - Module 5/6 : Analyses RNA-seq, bioinformatique- session Septembre 2021", "shortName": "", "description": "Bilille propose chaque année un cycle de formation d'introduction à l'analyse des données de séquençage à haut débit.\r\nCe cycle est composé de 6 modules, à la carte : \r\n- Module 1: Analyses ADN\r\n- Module 2: Analyses de variants\r\n- Module 3 : Métagénomique\r\n- Module 4: ChIP-seq\r\n- Module 5: Analyses RNA-seq, bioinformatique\r\n- Module 6: Analyses RNA-seq, biostatistique\r\nLes fiches descriptives sont accessibles sur le site de Bilille. Chaque module comprend des présentations générales et des séances pratiques sur ordinateur, avec Galaxy.\r\nLes objectifs du module 5 sont :\r\n- Savoir réaliser une analyse transcriptomique par RNA-seq avec ou sans (de novo) génome de référence à l’aide du portail Galaxy\r\n- Avoir un regard critique sur la qualité des lectures obtenues par le séquenceur\r\n- Connaître et savoir paramétrer les outils nécessaires à l’analyse", "homepage": "https://bilille.univ-lille.fr/training/training-offer", "is_draft": false, "costs": [ "Free" ], "topics": [], "keywords": [], "prerequisites": [ "Galaxy - Basic usage" ], "openTo": "Internal personnel", "accessConditions": "Etre familier avec la plate-forme web Galaxy (idéalement avoir suivi la formation bilille « Initiation à Galaxy »)\r\nAvoir suivi le module 1/5 « Analyses ADN » de ce cycle ou toute autre formation permettant de justifier de connaissances sur les données de séquençage haut débit et leur alignement.", "maxParticipants": null, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/487/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 52, "name": "CNRS", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/CNRS/?format=api" }, { "id": 56, "name": "INSERM", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INSERM/?format=api" }, { "id": 66, "name": "UDL", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/UDL/?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": "2024-12-09T17:35:45.084740Z", "type": "Training course", "start_date": "2021-09-16", "end_date": "2021-09-17", "venue": "", "city": "Villeneuve d'Ascq", "country": "FRANCE", "geographical_range": "", "trainers": [], "trainingMaterials": [], "computingFacilities": [], "realisation_status": "past", "registration_opening": null, "registration_closing": "2021-01-06", "registration_status": "closed", "courseMode": "Onsite" }, { "id": 548, "name": "Cycle « Analyse de données de séquençage à haut-débit » - Module 3/6 : Métagénomique - session Mai 2021", "shortName": "", "description": "Bilille propose chaque année un cycle de formation d'introduction à l'analyse des données de séquençage à haut débit.\r\nCe cycle est composé de 6 modules, à la carte : \r\n- Module 1: Analyses ADN\r\n- Module 2: Analyses de variants\r\n- Module 3 : Métagénomique\r\n- Module 4: ChIP-seq\r\n- Module 5: Analyses RNA-seq, bioinformatique\r\n- Module 6: Analyses RNA-seq, biostatistique\r\nLes fiches descriptives sont accessibles sur le site de Bilille. Chaque module comprend des présentations générales et des séances pratiques sur ordinateur, avec Galaxy.\r\nLes objectifs du module 3 sont :\r\n- Connaître les différentes méthodes de séquençage à haut débit pour la métagénomique, avec leurs avantages et leurs limites : métagénomique ciblée, métagénomique génomes entiers, métatranscriptomique\r\n- Comprendre les différentes étapes analytiques du traitement bioinformatique des données et savoir les mettre en œuvre\r\n- Savoir conduire une analyse statistique pour l’estimation de la richesse de la biodiversité\r\n- Aller jusqu’aux conclusions biologiques", "homepage": "https://bilille.univ-lille.fr/training/training-offer", "is_draft": false, "costs": [ "Free" ], "topics": [], "keywords": [], "prerequisites": [ "Galaxy - Basic usage" ], "openTo": "Internal personnel", "accessConditions": "- Etre familier avec la plate-forme web Galaxy (idéalement avoir suivi la formation bilille « Initiation à Galaxy »)\r\n- Avoir suivi le module 1/5 « Analyses ADN » de ce cycle ou toute autre formation permettant de justifier de connaissances sur les données de séquençage haut débit et leur alignement. Etre familier avec le vocabulaire et les étapes de base de l’analyse de données de séquençage : nettoyage, assemblage, mapping", "maxParticipants": null, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/487/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 52, "name": "CNRS", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/CNRS/?format=api" }, { "id": 56, "name": "INSERM", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INSERM/?format=api" }, { "id": 66, "name": "UDL", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/UDL/?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": "2024-12-09T17:35:55.483683Z", "type": "Training course", "start_date": "2021-05-26", "end_date": "2021-05-28", "venue": "", "city": "Villeneuve d'Ascq", "country": "FRANCE", "geographical_range": "", "trainers": [], "trainingMaterials": [], "computingFacilities": [], "realisation_status": "past", "registration_opening": null, "registration_closing": "2021-01-06", "registration_status": "closed", "courseMode": "Onsite" }, { "id": 547, "name": "Cycle « Analyse de données de séquençage à haut-débit » - Module 2/6 : Analyses de variants- session Mars 2021", "shortName": "", "description": "Bilille propose chaque année un cycle de formation d'introduction à l'analyse des données de séquençage à haut débit.\r\nCe cycle est composé de 6 modules, à la carte : \r\n- Module 1: Analyses ADN\r\n- Module 2: Analyses de variants\r\n- Module 3 : Métagénomique\r\n- Module 4: ChIP-seq\r\n- Module 5: Analyses RNA-seq, bioinformatique\r\n- Module 6: Analyses RNA-seq, biostatistique\r\nLes fiches descriptives sont accessibles sur le site de Bilille. Chaque module comprend des présentations générales et des séances pratiques sur ordinateur, avec Galaxy.\r\nLes objectifs du module 2 sont :\r\n- Comprendre les grands principes de la détection de variants\r\n- Réaliser les différentes étapes du post-traitement des données d’alignement à la détection de variants\r\n- Adapter l’analyse en fonction du type de données NGS générées\r\n- Comprendre la structure des données de variants\r\n- Savoir annoter des variants\r\n- Etre capable d’interpréter une liste de variants grâce aux outils libres disponibles", "homepage": "https://bilille.univ-lille.fr/training/training-offer", "is_draft": false, "costs": [ "Free" ], "topics": [], "keywords": [], "prerequisites": [ "Galaxy - Basic usage" ], "openTo": "Internal personnel", "accessConditions": "- Etre familier avec la plate-forme web Galaxy (idéalement avoir suivi la formation bilille « Initiation à Galaxy »)\r\n- Avoir suivi le module 1/5 « Analyses ADN » de ce cycle ou toute autre formation permettant de justifier de connaissances sur les données de séquençage haut débit et leur alignement", "maxParticipants": null, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/487/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 52, "name": "CNRS", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/CNRS/?format=api" }, { "id": 56, "name": "INSERM", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/INSERM/?format=api" }, { "id": 66, "name": "UDL", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/UDL/?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": "2024-12-09T17:36:14.949400Z", "type": "Training course", "start_date": "2021-03-24", "end_date": "2021-03-26", "venue": "", "city": "Lille", "country": "FRANCE", "geographical_range": "", "trainers": [], "trainingMaterials": [], "computingFacilities": [], "realisation_status": "past", "registration_opening": null, "registration_closing": "2021-01-06", "registration_status": "closed", "courseMode": "Onsite" }, { "id": 525, "name": "12ème Ecole de Bioinformatique AVIESAN-IFB-Inserm", "shortName": "EBAII 2023 niv1", "description": "La formation s’adresse à des biologistes directement impliqués dans des projets “Next Generation Sequencing” (NGS). Cette édition de l’école aborde les nouveaux enjeux technologiques: elle s’articulera autour de quatres ateliers thématiques en session parallèle (RNA-seq, ChIP-seq/ATAC-seq, variants DNA-seq, single-cell), et inclura une introduction à l’intégration des données, une ouverture aux technologies “long reads”.\r\n\r\nL’école vise à introduire les concepts et à manipuler les outils informatiques et à en interpréter les résultats. Elle est basée sur une alternance de courtes sessions théoriques et d’ateliers pratiques. Les participants bénéficieront d’un tutorat personnalisé pour élaborer leur plan d’analyse, et effectuer les premières étapes de traitement de leurs propres données ou de celles de leur plateforme.", "homepage": "https://ifb-elixirfr.github.io/EBAII/", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [ "Biostatistics", "Sequence analysis", "NGS Sequencing Data Analysis" ], "prerequisites": [], "openTo": "Everyone", "accessConditions": "La formation s’adresse à des biologistes directement impliqués dans des projets “Next Generation Sequencing” (NGS). \r\nAucune connaissance préalable des environnements Linux ou R n’est requise, mais il sera demandé aux participants de suivre une autoformation en ligne en amont, pour faciliter la prise en main de ces langages. 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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. 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