Whole genome sequencing
Whole genome sequencing is the broadest supported input because it covers much more of the genome than exome or SNP array data. It is usually the best fit when the goal is to inspect beyond a fixed marker list.
Whole exome sequencing
Whole exome sequencing focuses on protein-coding regions. It can still support gene and pathway review, especially when the question is centered on coding variants, but it can miss non-coding, regulatory, mitochondrial, and structural findings depending on the assay and pipeline.
Variant types
WGS and WES files may include single nucleotide variants, small insertions and deletions, genotype quality information, allele depth, and other annotations. Gene Inspector Pro can only display and interpret information that is present in the uploaded file and supported by the processing pipeline.
Use in Gene Inspector Pro
Use WGS when you want the most complete starting point for raw DNA review. Use WES when the available data is exome-only or when the review question is focused on coding genes. In both cases, findings should be interpreted with source quality, coverage, and professional context in mind.