Training List
Handles creating, reading and updating training events.
GET /api/training/?format=api&offset=360&ordering=accessConditions
{ "count": 383, "next": "https://catalogue.france-bioinformatique.fr/api/training/?format=api&limit=20&offset=380&ordering=accessConditions", "previous": "https://catalogue.france-bioinformatique.fr/api/training/?format=api&limit=20&offset=340&ordering=accessConditions", "results": [ { "id": 153, "name": "Cycle « Initiation à la bioinformatique » - Module 1/4 : Banques de données et Blast", "shortName": "", "description": "Bilille propose un cycle de découverte de la bioinformatique à destination des chercheur·euses, enseignant·es-chercheur·euses, ingénieur·es, technicien·nes et doctorant·es en biologie. Aucun pré-requis en informatique n'est attendu.\r\nLe cycle est constitué de quatre modules de deux jours:\r\n- Banques de données et BLAST\r\n- Alignement de séquences\r\n- Prédiction de gènes et annotation de protéines\r\n- Initiation à la reconstruction phylogénétique en biologie moléculaire\r\nCes modules peuvent être suivis indépendamment, mais ont une cohérence. Suivre chaque module peut aider à une meilleure compréhension des modules suivants.\r\nLes fiches descriptives des différents modules sont accessibles sur le site web de Bilille.\r\nLes objectifs du module 1 sont :\r\n- Découvrir différentes banques de données de séquences généralistes\r\n- Savoir interroger les banques de données et réaliser des requêtes pertinentes\r\n- Comprendre la structure des données\r\n- Savoir utiliser de manière optimale le logiciel Blast en fonction de l'application visée (ex : recherche d’homologie, prédiction de gènes…)\r\n- Etre capable d'analyser un résultat avec un regard critique", "homepage": "https://bilille.univ-lille.fr/training/training-offer", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Autre", "Sequence analysis", "Multiple sequence alignment", "Databases and information systems" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "Savoir utiliser un ordinateur (Windows...) : naviguer sur internet (Internet Explorer ou Firefox), utiliser un traitement de texte (Word ou OpenOffice).", "maxParticipants": null, "contacts": [], "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": "2024-12-09T17:42:24.618464Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [] }, { "id": 155, "name": "Cycle « Initiation à la bioinformatique » - Module 3/4 : Prédiction de gènes et annotation de protéines", "shortName": "", "description": "Bilille propose un cycle de découverte de la bioinformatique à destination des chercheur·euses, enseignant·es-chercheur·euses, ingénieur·es, technicien·nes et doctorant·es en biologie. Aucun pré-requis en informatique n'est attendu.\r\nLe cycle est constitué de quatre modules de deux jours:\r\n- Banques de données et BLAST\r\n- Alignement de séquences\r\n- Prédiction de gènes et annotation de protéines\r\n- Initiation à la reconstruction phylogénétique en biologie moléculaire\r\nCes modules peuvent être suivis indépendamment, mais ont une cohérence. Suivre chaque module peut aider à une meilleure compréhension des modules suivants.\r\nLes fiches descriptives des différents modules sont accessibles sur le site web de Bilille.\r\nLes objectifs du module 3 sont :\r\n- découvrir les logiciels liés à la prédiction de gènes et à l'annotation de protéines\r\n- acquérir la méthodologie pour prédire les gènes présents sur un génome qu'il soit bactérien ou eucaryote\r\n- acquérir la méthodologie pour analyser la séquence protéique prédite et en déduire la fonction possible de la protéine, avoir une idée de sa localisation cellulaire et de sa structure\r\n- être capable d'analyser les résultats obtenus par les logiciels avec un regard critique", "homepage": "https://bilille.univ-lille.fr/training/training-offer", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Autre", "Sequence analysis", "proteomics", "Sequence annotation", "Pattern matching", "Protein inference and validation" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "- Savoir utiliser un ordinateur (Windows...) : naviguer sur internet (Internet Explorer ou Firefox), utiliser un traitement de texte (Word ou OpenOffice).\r\n- Être familié avec les banques de données, Blast, formats de séquences et alignements de séquences (idéalement avoir suivi le module 1/4 « Banques de données et Blast » et le module 2/4 « Alignements de séquences » du cycle d'initiation à la bioinformatique).", "maxParticipants": null, "contacts": [], "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": "2024-12-09T17:42:03.687244Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [] }, { "id": 154, "name": "Cycle « Initiation à la bioinformatique » - Module 2/4 : Alignement de séquences", "shortName": "", "description": "Bilille propose un cycle de découverte de la bioinformatique à destination des chercheur·euses, enseignant·es-chercheur·euses, ingénieur·es, technicien·nes et doctorant·es en biologie. Aucun pré-requis en informatique n'est attendu.\r\nLe cycle est constitué de quatre modules de deux jours:\r\n- Banques de données et BLAST\r\n- Alignement de séquences\r\n- Prédiction de gènes et annotation de protéines\r\n- Initiation à la reconstruction phylogénétique en biologie moléculaire\r\nCes modules peuvent être suivis indépendamment, mais ont une cohérence. Suivre chaque module peut aider à une meilleure compréhension des modules suivants.\r\nLes fiches descriptives des différents modules sont accessibles sur le site web de Bilille.\r\nLes objectifs du module 2 sont :\r\n- Découvrir les différents types d'alignement pour les séquences protéiques et nucléiques\r\n- Savoir choisir le logiciel et les paramètres adaptés à une problématique (alignement local, global, multiple...)\r\n- Comprendre les méthodes algorithmiques pour l'alignement de séquences\r\n- Comprendre les paramètres des logiciels\r\n- Etre capable d'analyser un résultat d'alignement avec un regard critique", "homepage": "https://bilille.univ-lille.fr/training/training-offer", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Autre", "Sequence Algorithm", "Sequence analysis", "Pattern matching", "Multiple sequence alignment" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "- Savoir utiliser un ordinateur (Windows…) : naviguer sur internet (Internet Explorer ou Firefox), utiliser un traitement de texte (Word ou OpenOffice).\r\n- Etre familier avec les banques de données, Blast et formats de séquences (idéalement avoir suivi le module 1/4 « Banques de données et Blast » du cycle d'initiation à la bioinformatique).", "maxParticipants": null, "contacts": [], "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": "2024-12-09T17:42:17.819204Z", "audienceTypes": [], "audienceRoles": [], "difficultyLevel": "", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": null, "hoursHandsOn": null, "hoursTotal": null, "personalised": null, "event_set": [] }, { "id": 49, "name": "Introduction to molecular phylogeny", "shortName": "", "description": "Training organized by CNRS Entreprises\n", "homepage": "https://cnrsformation.cnrs.fr/stage-17008-Phylogenie-moleculaire-%28Lyon%29.html", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Phylogeny", "Evolution and Phylogeny", "Molecular evolution", "Tree of Life", "Phylogenomics", "Genes and genomes" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "Some knowledge in mathematics and statistics.\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": 144, "name": "FROGS formation : tools for bioinformatics and statistics analyses with amplicon metagenomics data", "shortName": "", "description": "This training session, organized by Bioinfo Genotoul, Sigenae, NED (GenPhySE) and TWB, is designed to help you to deal with NGS data of 16S, 18S ... 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/events/metagenomic-amplicons-and-stats-with…", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [ "NGS Data Analysis", "Metagenomics", "metatranscriptomics", "Galaxy" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "Subscribe by the web page : http://bioinfo.genotoul.fr/index.php/training-2/galaxy-training/.\nPrices : 165 euros per day for academic people, 550 per day otherwise.\n", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [], "logo_url": "https://ressources.france-bioinformatique.fr/sites/default/files/FROGS_logo_0.png", "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/273/?format=api" ] }, { "id": 303, "name": "Tools for phylogenetic analysis", "shortName": "", "description": "You will learn How to find homologs, make multiple alignments, reconstruct the phylogeny, visualize the tree.\r\n\r\nAt the end of the workshop, you will be able to use web tools to reconstruct accurate phylogenies.\r\n\r\nUnless all participants speak French, the course will be taught in English.", "homepage": "https://pliniuscursus.univ-amu.fr/formation/tools-for-phylogenetic-analysis/", "is_draft": false, "costs": [ "Free to academics" ], "topics": [ "http://edamontology.org/topic_0084" ], "keywords": [], "prerequisites": [ "Master" ], "openTo": "Internal personnel", "accessConditions": "The first sessions are only available for IM2B students.", "maxParticipants": 10, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 38, "name": "IGS - Laboratoire Information Génomique et Structurale", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/IGS%20-%20Laboratoire%20Information%20G%C3%A9nomique%20et%20Structurale/?format=api" } ], "organisedByTeams": [ { "id": 23, "name": "PACA-Bioinfo", "url": "https://catalogue.france-bioinformatique.fr/api/team/PACA-Bioinfo/?format=api" } ], "logo_url": null, "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [ "Graduate" ], "audienceRoles": [ "Biologists" ], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": 1, "hoursHandsOn": 5, "hoursTotal": 6, "personalised": null, "event_set": [] }, { "id": 289, "name": "Introduction to galaxy: looking for variants in prokaryotes", "shortName": "Introduction to galaxy", "description": "This course will focus on the technical aspects of using a galaxy server. Accessible without any prerequisite in computer science, it will allow you to master the different fundamental tools of galaxy and will open the doors of bioinformatics analysis for your different projects.\r\nDifferent questions will be addressed through an example of variants analysis in a prokaryotic organism. At the end of this course, on any accessible galaxy instance, you will be able to:\r\n- upload your data\r\n- map them on a reference genome\r\n- find the variants (SNPs) and analyze the results\r\n- generate, manipulate and share your workflows, data and histories\r\n- find the right tools for other analyses and use them in your own project.\r\n\r\nUnless all participants speak French, the course will be taught in English.", "homepage": "https://pliniuscursus.univ-amu.fr/formation/galaxy-platform/", "is_draft": false, "costs": [ "Free to academics" ], "topics": [ "http://edamontology.org/topic_0091", "http://edamontology.org/topic_0622" ], "keywords": [], "prerequisites": [ "Master" ], "openTo": "Internal personnel", "accessConditions": "The first sessions are only available for IM2B students.", "maxParticipants": 12, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [], "organisedByTeams": [ { "id": 23, "name": "PACA-Bioinfo", "url": "https://catalogue.france-bioinformatique.fr/api/team/PACA-Bioinfo/?format=api" } ], "logo_url": null, "updated_at": "2022-06-02T11:50:50.812642Z", "audienceTypes": [ "Graduate" ], "audienceRoles": [ "Biologists" ], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "", "hoursPresentations": 1, "hoursHandsOn": 5, "hoursTotal": 6, "personalised": null, "event_set": [] }, { "id": 290, "name": "NGS data analysis on the command line", "shortName": "NGS-analysis-cli", "description": "This hands-on course will teach bioinformatic approaches for analyzing Illumina sequencing data. Our goal is to introduce the command line skills you need to make the most of your NGS data. \r\nDuring this 4-day training we will first introduce the Linux environment, shell commands and basic R scripting. And then we will focus on two NGS data analyses -- small RNA-seq and RNA-seq -- based on published datasets from the model organism Arabidopsis thaliana", "homepage": "https://www.ibmp.cnrs.fr/bioinformatics-trainings/", "is_draft": false, "costs": [ "Free to academics" ], "topics": [ "http://edamontology.org/topic_0102", "http://edamontology.org/topic_3170", "http://edamontology.org/topic_2269", "http://edamontology.org/topic_3168" ], "keywords": [], "prerequisites": [ "none" ], "openTo": "Internal personnel", "accessConditions": "This training is dedicated to academics working in a laboratory of Unistra/CNRS.", "maxParticipants": 12, "contacts": [ "https://catalogue.france-bioinformatique.fr/api/userprofile/124/?format=api" ], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 79, "name": "IBMP", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/IBMP/?format=api" } ], "organisedByTeams": [ { "id": 14, "name": "BiGEst", "url": "https://catalogue.france-bioinformatique.fr/api/team/BiGEst/?format=api" } ], "logo_url": null, "updated_at": "2024-01-22T14:51:37.215331Z", "audienceTypes": [], "audienceRoles": [ "Biologists", "Bioinformaticians" ], "difficultyLevel": "Novice", "trainingMaterials": [], "learningOutcomes": "Applied Knowledge (Know-how):\r\n- Basic proficiency at the Linux command line prompt\r\n- Basic proficiency of R (environment, objects, graphs) \r\n- Next generation sequencing (NGS) file formats; reference genomes - Mapping NGS read data to reference genomes (bowtie, samtools)\r\n- Small RNA-seq analysis; epigenomics applications (ShortStack)\r\n- RNA-seq for transcriptomics; differential gene expression analysis (HISAT2, DESeq2) - Data wrangling and visualization in R (Rstudio, ggplot2)", "hoursPresentations": 12, "hoursHandsOn": 16, "hoursTotal": 28, "personalised": null, "event_set": [ "https://catalogue.france-bioinformatique.fr/api/event/503/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/504/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/589/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/454/?format=api", "https://catalogue.france-bioinformatique.fr/api/event/660/?format=api" ] }, { "id": 143, "name": "Training on annotation of transposable elements", "shortName": "", "description": "The objectives of this training are: \nTo acquire knowledge on transposable elements\nTo achieve annotation of transposable elements in the genome using REPET pipelines\nTo be autonomous on your own data.\nProgram\nOpening presentations on transposable elements and their annotation\nStrategies of repeat annotation\nREPET pipelines overview and practices \nPost-analyze tools overview and practices\n \n", "homepage": "https://urgi.versailles.inra.fr/Platform/Training/Training-on-annotation-of-tran…", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [ "Bioinformatics and Plant Genomics", "Sequence analysis" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "This training is dedicated to biologists and/or bioinformaticians (10 pers. max)\nCost : 150€\nRegistration and information by mail to: urgi-contact@inra.fr\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/272/?format=api" ] }, { "id": 270, "name": "Command line inititation", "shortName": "", "description": "Objectives :\n Knowing the principles and advantages of the Linux system\n Knowing how to use the main bash commands\n Knowing how to launch programs with arguments\n Acquiring autonomy to perform bioinformatics analysis on the command line.\n", "homepage": "http://www.pf-bird.univ-nantes.fr/training/", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [ "Cluster", "Computing Environments" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "This training is open to all (public and private) with no institution restrictions and is accessible through the University of Nantes continuing education programme.\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": 42, "name": "Initiation to R language", "shortName": "", "description": "OBJECTIVES :\n* Acquire basic knowledge on the R language\n* Experience the main features of R\n* Be autonomous in handling data\n* Perform simple statistical analysis and build charts\n* Learn how to create functions\n", "homepage": "http://www.pf-bird.univ-nantes.fr/training/", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [ "Programming Languages & Computer Sciences", "R Language" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "This training is open to all (public and private) with no institution restrictions and is accessible through the University of Nantes continuing education programme.\n", "maxParticipants": null, "contacts": [], "elixirPlatforms": [], "communities": [], "sponsoredBy": [], "organisedByOrganisations": [ { "id": 55, "name": "University of Nantes", "url": "https://catalogue.france-bioinformatique.fr/api/organisation/University%20of%20Nantes/?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": [] }, { "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": "http://www.pf-bird.univ-nantes.fr/training/", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [ "Autre", "Gene expression differential analysis", "Galaxy", "Transcriptomics (RNA-seq)" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "This training is open to all (public and private) with no institution restrictions and is accessible through the University of Nantes continuing education programme.\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": 73, "name": "Galaxy : RNASeq alignment and transcripts assemblies", "shortName": "", "description": "As the command line training but with Galaxy. Organized jointly by the Sigenae and the Bioinfo Genotoul platforms.\n", "homepage": "http://bioinfo.genotoul.fr/index.php/events/rnaseq-alignment-and-transcripts-ass…", "is_draft": false, "costs": [], "topics": [], "keywords": [ "NGS Data Analysis", "Analysis of RNAseq data", "Gene expression differential analysis", "Galaxy", "Transcript and transcript variant analysis", "Transcriptomics (RNA-seq)", "NGS Sequencing Data Analysis" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "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": 72, "name": "Galaxy : Reads alignment and SNP calling", "shortName": "", "description": "As the command line training but with Galaxy. Organized jointly by the Sigenae and bioinfo genotoul platforms.\n", "homepage": "http://bioinfo.genotoul.fr/index.php/events/reads-alignment-and-small-size-varia…", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [ "NGS Data Analysis", "Galaxy", "Variant analysis", "Genomics (DNA-seq)", "NGS Sequencing Data Analysis" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "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": [ "https://catalogue.france-bioinformatique.fr/api/event/262/?format=api" ] }, { "id": 74, "name": "Galaxy : sRNAseq", "shortName": "", "description": "As the command line training but with Galaxy. Organized jointly by the Sigenae and Bioinfo Genotoul platforms.\n", "homepage": "http://bioinfo.genotoul.fr/index.php/events/srnaseq/", "is_draft": false, "costs": [], "topics": [], "keywords": [ "NGS Data Analysis", "Small and long non-coding RNAs", "Analysis of RNAseq data", "Galaxy" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "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": 68, "name": "Sequences alignment and phylogeny ", "shortName": "", "description": "This training session is organized by the bios4Biol CATI and the genotoul bioinfo platform and aims at initiating participants to molecular phylogenetics studies.\nYou will discover how to build a sequence dataset, to align sequences, to edit and refine the resulting alignment.\n", "homepage": "http://bioinfo.genotoul.fr/index.php/events/sequences-alignment-phylogeny/", "is_draft": false, "costs": [], "topics": [], "keywords": [], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "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": 67, "name": "RNAseq de novo assembly", "shortName": "", "description": "This training session has been designed to give you an overview of the methods and tools used to de novo assemble transcriptomic short reads. You will learn how to pre-process your raw data (fastq files), how an assembler works and how to use it. Finally you will learn how to assess the quality of your assemblies in order to choose the best one. Organized jointly by the Sigenae and bioinfo genotoul platforms.\n", "homepage": "http://bioinfo.genotoul.fr/index.php/events/rnaseq-de-novo-assembly-2/", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [ "NGS Data Analysis", "Analysis of RNAseq data", "Transcript and transcript variant analysis", "Transcriptomics (RNA-seq)", "Sequence annotation" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "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": 64, "name": "Read alignment and SNP calling", "shortName": "", "description": "This training session, organized jointly with the Sigenae platform, is designed to help you deal with NGS data, in particular Roche 454 and Illumina Solexa technologies. You will discover the new sequence formats, the new assembly formats and the known biases of these technologies. You will use mapping on reference genome software, polymorphisms detection (with the GATK pipeline), polymorphisms annotation and alignment visualization software. Organized jointly by the Sigenae and bioinfo genotoul platforms.\n", "homepage": "http://bioinfo.genotoul.fr/index.php/events/alignment-and-small-size-variants-ca…", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [ "NGS Data Analysis", "Variant analysis", "Genomics (DNA-seq)" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "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": 71, "name": "Galaxy : first step", "shortName": "", "description": "Galaxy is a workbench available for biologists from Sigenae Platform. Galaxy objectives are:\n First, making bioinfo Linux tools accessible to biologists.\n Then, it is possible to add Linux tools by developpers into Galaxy workbench.\n Then, Galaxy is used to hide the complexity of the infrastructure and to allow creation, execution and sharing of workflows.\nYou will acquire the following competencies required for the other Galaxy trainning:\n Login to Galaxy: Galaxy Workbench (To access to Galaxy, you need to have an LDAP Genotoul login and password).\n Begin to use some tools provided (BWA, SAM tools, FastQC).\n Work on files.\nOrganized jointly by the Sigenae and the Bioinfo Genotoul platform.\n", "homepage": "http://bioinfo.genotoul.fr/index.php/events/first-step-with-galaxy/", "is_draft": false, "costs": [ "Priced" ], "topics": [], "keywords": [ "Web portals", "Galaxy", "Interfaces", "NGS Sequencing Data Analysis" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "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": 70, "name": "Phylogenomy and selection pressure ", "shortName": "", "description": "This training session is organized by the bios4Biol CATI.\nMorning : phylogenomics\nThe morning course will provide insigths about sampling problems in phylogenomics studies (genes, species) and methodological aspects of phylogenomics studies with two major focus on super-matrix and super-tree methods.\nAfternoon : selection pressure\nThe afternoon course will be dedicated to the use of the PAML4 package in order to study selection pressures in a sequence alignment.\n", "homepage": "http://bioinfo.genotoul.fr/index.php/events/phylogenomics-and-selection-pressure…", "is_draft": false, "costs": [], "topics": [], "keywords": [ "Phylogeny", "Evolution and Phylogeny", "Molecular evolution", "Selection Detection", "Phylogenomics", "Genes and genomes" ], "prerequisites": [], "openTo": "Internal personnel", "accessConditions": "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": [] } ] }
