- Home
- Materials
Filters
Sort
-
-
Filter Clear filters
-
-
Operation
- Alignment1
- Alignment construction1
- Alignment generation1
- Allele calling1
- Exome variant detection1
- Genome 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
- Show N_FILTERS more
-
-
-
Content provider
- Swiss Institute of Bioinformatics1
- Show N_FILTERS more
-
-
-
Keyword
- NGS bioinformatics
- Variant Analysis17
- one-health5
- virology4
- Introduction3
- Variants3
- microgalaxy3
- prokaryote3
- Human genetic variation2
- covid192
- Variant-calling1
- BioMart1
- ELIXIR RIR, BridgeDb1
- EVA1
- GWAS1
- Gene transcripts1
- Genetic variation databases1
- Genome sequencing1
- Mutations1
- SNPs1
- Sequence alignments1
- Tools1
- VEP1
- Variant calling1
- Variation1
- coronavirus1
- cyoa1
- gmod1
- jbrowse11
- tuberculosis1
- Show N_FILTERS more
-
-
-
Difficulty level
- Beginner1
- Show N_FILTERS more
-
-
-
Resource type
- Computer Software1
- workflow1
- Show N_FILTERS more
-
- Show archived materials