The variant visualization tool in Emedgene provides a high-resolution, interactive genomic context for variant interpretation. It supports multiple variant types—SNVs, Indels, CNVs, STRs, MRJD, and Targeted Caller Variants—while integrating population data, functional predictions, curated annotations, and sequencing evidence.
An IGV-based customizable viewer enables visual review of alignment and annotation data for validation and interpretation of variant calls.
