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- Scientific topic
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- DNA variation1
- Genetic variation1
- Genomic variation1
- Mutation1
- Pipelines1
- Polymorphism1
- Software integration1
- Somatic mutations1
- Tool integration1
- Virology1
- Workflows1
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- Operation
- Genome variant detection
- Alignment1
- Alignment construction1
- Alignment generation1
- Allele calling1
- Exome variant detection1
- Germ line variant calling1
- Mutation detection1
- Read pre-processing1
- Sequence read pre-processing1
- Somatic variant calling1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
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- Tool
- V-pipe1
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- Content provider
- SIB Swiss Institute of Bioinformatics1
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- Keyword
- NGS bioinformatics
- Variant-calling1
- coronavirus1
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- Competency level
- Beginner1
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- Licence
- Creative Commons Attribution Share Alike 4.0 International1
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- Target audience
- Biologists, Genomicists, Computer Scientists1
- bioinformaticians1
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- Author
- Ivan Topolsky1
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- Resource type
- Computer Software1
- workflow1
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- Node
- Switzerland1
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