MiModD

MiModD maps and annotates mutations from whole-genome sequencing (WGS) data to identify causal variants in genetic studies.

Key Features:

• Versatility: Supports multiple mapping-by-sequencing protocols.
• WGS data support: Analyzes whole-genome sequencing (WGS) data for variant discovery.
• Mutation analysis: Performs mapping, identification, and annotation of mutations.

Scientific Applications:

• Mutation mapping in model organisms: Uses WGS to pinpoint mutations associated with phenotypic changes in model organisms.
• Genetics, genomics, and evolutionary biology: Facilitates identification and annotation of causal variants for studies in genetics, genomics, and evolutionary biology.

Methodology:

Analyzes WGS data using mapping-by-sequencing protocols to map, identify, and annotate mutations.