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- Scientific topic
- Bioinformatics1
- DNA structural variation1
- Deletion1
- Duplication1
- Exomes1
- Genome annotation1
- Genomes1
- Genomic structural variation1
- Genomics1
- Insertion1
- Inversion1
- Personal genomics1
- Structural variation1
- Synthetic genomics1
- Translocation1
- Viral genomics1
- Whole genomes1
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- Operation
- Structural genome annotation
- Alignment1
- Alignment construction1
- Alignment generation1
- Allele calling1
- Exome variant detection1
- Functional genome annotation1
- Genome annotation1
- Genome variant detection1
- Germ line variant calling1
- Metagenome annotation1
- Mutation detection1
- Normalisation1
- Read pre-processing1
- Sequence classification1
- Sequence read pre-processing1
- Somatic variant calling1
- Standardisation1
- Standardisation and normalisation1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
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- Tool
- PASTEClassifier1
- REPET1
- REXdb1
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- Content provider
- IFB French Institute of Bioinformatics1
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- Keyword
- Annotation1
- Docker1
- Pipelines1
- Transposons1
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- Competency level
- Beginner
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- Licence
- Creative Commons Attribution Non Commercial No Derivatives 4.0 International1
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- Target audience
- Biologists, Genomicists, Computer Scientists
- Bioinformatician1
- Scientists1
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- Author
- Johann Confais1
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- Contributor
- INRAE1
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- Resource type
- Bioinformatics1
- Training materials1
- Tutorial1
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- Related resource
- REPET image Docker1
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- Node
- France1
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- Status
- Active1
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