Event List
Handles creating, reading and updating events.
GET /api/event/?format=api&offset=260&ordering=-elixirPlatforms
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The meeting will put the emphasis on methods and models for phylogenomics and population genomics. Beyond this year's themes, general concepts, models, methods and algorithms will be presented and discussed, just as in the previous editions of MCEB. As usual, the meeting will bring together researchers originating from various disciplines: mathematics, statistics, computer science, phylogenetics, population genetics, molecular epidemiology, biodiversity and macroevolution... Keynote speakers will\r\nintroduce a field of research and discuss their own work in this field. Afternoon will be for short presentations and posters, with plenty of time for discussions. We will stop early every day, thus leaving time for other activities.\r\n\r\nKEYNOTES:\r\n** Sophie Abby - \"Evolution of biosynthetic pathways in Bacteria\"\r\n** Richard Durbin - \"Population genome variation – going beyond SNPs\"\r\n** Lisa Pokorny Montero - \"Genomic approaches to the study of plant evolution\"\r\n** Harald Ringbauer - \"Advanced ancient DNA analysis\"\r\n** Kristina Wicke - \"Inference of phylogenetic networks\"\r\n** Jaime Huerta-Cepas - \"Evolutionary significance of unknown microbial genes\"", "homepage": "https://mceb2025.sciencesconf.org/", "is_draft": false, "costs": [ "Priced" ], "topics": [ "http://edamontology.org/topic_2269", "http://edamontology.org/topic_3293", "http://edamontology.org/topic_3050", "http://edamontology.org/topic_3056" ], "keywords": [ "Biostatistics", "Biodiversity", "Evolution and Phylogeny", "Phylogenetics" ], "prerequisites": [], "openTo": "Everyone", "accessConditions": "PRACTICAL INFORMATION\r\n\r\n** Place: \"Carmen de la Victoria\" and \"Corrala de Santiago\", Granada, Spain.\r\n\r\n** Dates: May 12-16th, 2025. The conference will begin Monday evening and will\r\n end at about 3pm on Friday.\r\n\r\n** Fees: Between 650€ to 850€. Fees will vary depending on the type of room,\r\n shared (for students) or individual. They include accommodation for four nights\r\n with breakfast, lunches, coffee breaks, two dinners and drinks around posters\r\n from Monday night until Friday lunchtime included.\r\n\r\n** Deadline for abstract submission and pre-registration: February 21, 2025.\r\n\r\n** Notification of acceptance: March 15, 2025.", "maxParticipants": 60, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [ { "id": 7, "name": "ATGC", "url": "https://catalogue.france-bioinformatique.fr/api/team/ATGC/?format=api" } ], "logo_url": null, "updated_at": "2025-02-17T08:51:35.482439Z", "type": "Meeting", "start_date": "2025-05-12", "end_date": "2025-05-16", "venue": "Carmen de la Victoria\" and \"Corrala de Santiago\"", "city": "Granada", "country": "Spain", "geographical_range": "International", "trainers": [], "trainingMaterials": [], "computingFacilities": [], "realisation_status": "future", "registration_opening": "2025-02-01", "registration_closing": "2025-05-05", "registration_status": "open", "courseMode": "Onsite" }, { "id": 78, "name": "RNASeq with Galaxy", "shortName": "", "description": "", "homepage": "", "is_draft": false, "costs": [], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "https://ressources.france-bioinformatique.fr/sites/default/files/150x150.png", "updated_at": "2022-06-02T11:50:50.627601Z", "type": "Training course", "start_date": "2017-05-22", "end_date": "2017-05-23", "venue": "", "city": "Roscoff", "country": "", "geographical_range": "", "trainers": [], "trainingMaterials": [], "computingFacilities": [], "realisation_status": "past", "registration_opening": null, "registration_closing": null, "registration_status": "unknown", "courseMode": null }, { "id": 278, "name": "Cycle « Analyse de données de séquençage à haut-débit » - Module 1/5 : Analyses ADN", "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 5 modules, à la carte : \r\n- Module 1: Analyses ADN\r\n- Module 2: Analyses de variants\r\n- Module 3: Analyses RNA-seq, bioinformatique\r\n- Module 4: Analyses RNA-seq, biostatistique\r\n- Module 5: Métagénomique\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 1 sont :\r\n- Apprendre à manipuler des données de séquençage d’ADN\r\n- Réaliser des contrôles de qualité et du nettoyage des lectures\r\n- Présenter les méthodes et outils d'alignement\r\n- Réaliser des contrôles de qualité et des alignements sur une référence\r\n- Introduction à l’assemblage des lectures sans référence\r\n- Utiliser la plateforme Galaxy pour ces analyses", "homepage": "https://bilille.univ-lille.fr/training/training-offer", "is_draft": false, "costs": [ "Free" ], "topics": [], "keywords": [ "NGS Data Analysis", "Assembly of genomes and transcriptomes", "Read alignment on genomes", "NGS Sequencing Data Analysis" ], "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 »)", "maxParticipants": null, "contacts": [], "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": "2024-12-09T17:38:35.576886Z", "type": "Training course", "start_date": "2019-03-06", "end_date": "2019-03-07", "venue": "", "city": "Villeneuve d'Ascq", "country": "", "geographical_range": "", "trainers": [], "trainingMaterials": [], "computingFacilities": [], "realisation_status": "past", "registration_opening": null, "registration_closing": "2019-02-15", "registration_status": "closed", "courseMode": "Onsite" }, { "id": 603, "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": "https://bird.univ-nantes.io/website/images/logo/logo.svg", "updated_at": "2024-02-19T09:37:13.928843Z", "type": "Training course", "start_date": "2024-03-20", "end_date": "2024-03-21", "venue": "", "city": "Nantes", "country": "", "geographical_range": "", "trainers": [], "trainingMaterials": [], "computingFacilities": [], "realisation_status": "past", "registration_opening": "2024-02-08", "registration_closing": "2024-03-18", "registration_status": "closed", "courseMode": "Onsite" }, { "id": 637, "name": "Introduction à l'analyse de données transcriptomiques avec Galaxy", "shortName": "", "description": "L’objectif est de se familiariser avec les étapes d’analyses des données transcriptomiques ou RNA-seq avec référence pour extraire les gènes et fonctions différentiellement exprimés. Nous proposons au personnel non-bioinformaticien de les accompagner dans la prise en main de ces étapes d’analyses en utilisant la plateforme de bio-analyse Galaxy. \r\n\r\n\r\nAprès une introduction à la transcriptomique, une session pratique sur la plateforme Galaxy couvrira comment :\r\n- évaluer la qualité des données transcriptomiques,\r\n- aligner des données transcriptomiques sur un génome de référence,\r\n- estimer le nombre de séquences par gènes,\r\n- construire et faire une analyse d’expression différentielle des gènes\r\n- faire une analyse de l’enrichissement fonctionnel des gènes différentiellement exprimés", "homepage": "", "is_draft": false, "costs": [ "Free to academics" ], "topics": [ "http://edamontology.org/topic_3170", "http://edamontology.org/topic_0203", "http://edamontology.org/topic_3308", "http://edamontology.org/topic_1775" ], "keywords": [ "Galaxy", "RNA-seq", "Transcriptomics (RNA-seq)" ], "prerequisites": [ "Galaxy - Basic usage" ], "openTo": "Internal personnel", "accessConditions": "Formation ouverte au personnel de l’UCA & Associés\r\nAvoir un ordinateur portable et un accès wifi eduroam\r\nAvoir un compte sur la plateforme Galaxy (Faire une demande le cas échéant sur hub.mesocentre.uca.fr)\r\nÊtre familier avec Galaxy", "maxParticipants": null, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/677/?format=api", "https://catalogue.france-bioinformatique.fr/api/userprofile/807/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [ { "id": 1, "name": "CNRS - IFB", "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/CNRS%20-%20IFB/?format=api" }, { "id": 16, "name": "Université Clermont Auvergne", "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/Universit%C3%A9%20Clermont%20Auvergne/?format=api" } ], "organisedByOrganisations": [ { "id": 87, "name": "AuBi", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/AuBi/?format=api" }, { "id": 96, "name": "Mésocentre Clermont-Auvergne", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/M%C3%A9socentre%20Clermont-Auvergne/?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": "2024-06-06T08:09:16.432369Z", "type": "Training course", "start_date": "2024-07-18", "end_date": "2024-07-18", "venue": "Bâtiment Turing, Salle A009", "city": "Clermont-Ferrand", "country": "France", "geographical_range": "Local", "trainers": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/522/?format=api", "https://catalogue.france-bioinformatique.fr/api/userprofile/677/?format=api", "https://catalogue.france-bioinformatique.fr/api/userprofile/807/?format=api" ], "trainingMaterials": [ { "id": 144, "name": "Reference-based RNA-Seq data analysis with Galaxy", "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/Reference-based%20RNA-Seq%20data%20analysis%20with%20Galaxy/?format=api" }, { "id": 145, "name": "Introduction to Transcriptomics", "url": "https://catalogue.france-bioinformatique.fr/api/trainingmaterial/Introduction%20to%20Transcriptomics/?format=api" } ], "computingFacilities": [], "realisation_status": "past", "registration_opening": "2024-06-06", "registration_closing": "2024-06-20", "registration_status": "closed", "courseMode": "Onsite" }, { "id": 289, "name": "Metagenomic amplicon analysis with stats", "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": "2022-06-02T11:50:50.627601Z", "type": "Training course", "start_date": "2017-07-02", "end_date": "2017-07-05", "venue": "", "city": "Salle de formation Inra", "country": "", "geographical_range": "", "trainers": [], "trainingMaterials": [], "computingFacilities": [], "realisation_status": "past", "registration_opening": null, "registration_closing": null, "registration_status": "unknown", "courseMode": null }, { "id": 133, "name": "ELIXIR Innovation and SME Forum: Data Driven Innovation in Rare Diseases and Personalised Medicine", "shortName": "", "description": "IFB will host the next ELIXIR Innovation and SME Forum: Data Driven Innovation in Rare Diseases & Personalised Medicine.", "homepage": "https://www.elixir-europe.org/events/elixir-innovation-and-sme-forum-data-driven…", "is_draft": false, "costs": [], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "https://ressources.france-bioinformatique.fr/sites/default/files/elixir_node_france.png", "updated_at": "2022-06-02T11:50:50.627601Z", "type": "Conference", "start_date": "2017-11-14", "end_date": null, "venue": "", "city": "Paris, France", "country": "", "geographical_range": "", "trainers": [], "trainingMaterials": [], "computingFacilities": [], "realisation_status": "past", "registration_opening": null, "registration_closing": null, "registration_status": "unknown", "courseMode": null }, { "id": 279, "name": "Cycle « Analyse de données de séquençage à haut-débit » - Module 4/5 : Analyses RNA-seq - partie 2 (biostatistique)", "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 5 modules, à la carte : \r\n- Module 1: Analyses ADN\r\n- Module 2: Analyses de variants\r\n- Module 3: Analyses RNA-seq, bioinformatique\r\n- Module 4: Analyses RNA-seq, biostatistique\r\n- Module 5: Métagénomique\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 4 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": [ "NGS Data Analysis", "Transcriptomics (RNA-seq)", "NGS Sequencing Data Analysis" ], "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 2/5 «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": [], "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": "2024-12-09T17:38:26.986303Z", "type": "Training course", "start_date": "2019-09-15", "end_date": "2019-09-16", "venue": "", "city": "Villeneuve d'Ascq", "country": "", "geographical_range": "", "trainers": [], "trainingMaterials": [], "computingFacilities": [], "realisation_status": "past", "registration_opening": null, "registration_closing": "2019-02-15", "registration_status": "closed", "courseMode": "Onsite" }, { "id": 100, "name": " JDEV 2017 inscriptions et appel à communications ", "shortName": "", "description": "Les sujets abordés aux Journées du développement logiciel tournent autour du bigdata, du web-sémantique du traitement des données", "homepage": "http://www.jdev2017.fr", "is_draft": false, "costs": [], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "https://ressources.france-bioinformatique.fr/sites/default/files/jdevlogo2017_min.png", "updated_at": "2022-06-02T11:50:50.627601Z", "type": "Conference", "start_date": "2017-07-04", "end_date": "2017-07-07", "venue": "", "city": "Marseille centre", "country": "", "geographical_range": "", "trainers": [], "trainingMaterials": [], "computingFacilities": [], "realisation_status": "past", "registration_opening": null, "registration_closing": null, "registration_status": "unknown", "courseMode": null }, { "id": 416, "name": "Principes FAIR dans un projet de bioinformatique - Session 2021", "shortName": "FAIR bioinfo - 2021", "description": "L’Institut Français de Bioinformatique (IFB) organise en partenariat avec l’Institut de Biologie Intégrative de la Cellule (I2BC) une formation à destination des bioinformaticiens et biostatisticiens souhaitant mettre en oeuvre les principes “FAIR” (Facile à trouver, Accessible, Interopérable, Réutilisable) dans leurs projets d’analyse et de développement. Les concepts FAIR, initialement définis dans le contexte d’ouverture des données de la recherche, seront ici adaptés pour cadrer avec un projet type de développement et/ou analyse bioinformatique/biostatistique. Ainsi, la formation n’abordera pas les aspects “FAIR” spécifiques aux données mais introduira plusieurs outils permettant d’améliorer la reproductibilité des analyses.", "homepage": "https://ifb-elixirfr.github.io/IFB-FAIR-bioinfo-training/", "is_draft": false, "costs": [ "Priced" ], "topics": [ "http://edamontology.org/topic_0769" ], "keywords": [ "Computing Environments", "NGS Sequencing Data Analysis", "Workflow development" ], "prerequisites": [], "openTo": "Everyone", "accessConditions": "", "maxParticipants": null, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/116/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [ { "id": 3, "name": "IFB", "url": "https://catalogue.france-bioinformatique.fr/api/eventsponsor/IFB/?format=api" } ], "organisedByOrganisations": [ { "id": 43, "name": "IFB-core", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/IFB-core/?format=api" }, { "id": 64, "name": "I2BC", "url": 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