Handles creating, reading and updating training materials.

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            "name": "Application of RDF-based models and tools for enhancing interoperable",
            "description": "\n \n\nApplication of RDF-based models and tools for enhancing interoperable use of biomedical resources\n \n",
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            "name": "Cross Taxa Tutorial",
            "description": "How query databases according to complex taxonomic critera\nCross-Taxa allows to retrieve gene families that are shared by a given set of taxa, or which are specific to a set of taxa. It is also possible to select genes families which are associated to a certain set of taxa but which are not found in a second set of taxa. Any taxonomic level can be used.\n",
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            "description": "Cette formation a pour but de vous aider à traiter les séquences courtes issues des plates-formes de séquençage Illumina. Vous y découvrirez les formats de séquences et d’alignement les biais connus et mettrez en œuvre des logiciels d'alignement épissé sur génome de référence, la recherche de nouveaux gènes, de nouveaux transcrits et la quantification de l'expression de ces gènes et transcrits.",
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            "name": "Enrichment and propagation of metagenomic experimental metadata",
            "description": "\n \n\nEnrichment and propagation of metagenomic experimental metadata\n \n",
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            "name": "RNA-Seq: Differential Expression Analysis",
            "description": "\n \n\nBe careful about experimental design : avoid putting all the\nreplicates in the same lane, using the same barcode for the\nreplicates, putting different number of samples in lanes etc...\nNon- uniformity of the per base read distribution (Illumina Random\nHexamer Priming bias visible on the 13 first bases)\nBias hierarchy : biological condition >> concentration > run/flowcell> lane\nAt equivalent expression level, a long gene will have more reads than a short one.\nNon random coverage along the transcript.\nMultiple hit for some reads alignments.\n \n",
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            "description": "Detection of Copy Number Variations\n \n",
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            "name": "Improve Orphanet disease description knowledge by phenotypic automated recognition using scrapping toolkits",
            "description": "\n \n\nImprove Orphanet disease description knowledge by phenotypic automated recognition using scrapping toolkits\n \n",
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            "name": "Variants: alignment and pre-treatment; GATK",
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