Genomics
Whole Genome Sequencing (NeuraGenome)
Complete genomic analysis including coding and non-coding regions
Whole genome sequencing (WGS) offers the most comprehensive look at an individual’s DNA — including non-coding and regulatory regions that may explain complex or unsolved conditions.
$1,999.00
Overview
- Genome-wide coverage
- Detects structural variants and regulatory changes
- Best for unresolved or complex cases
Whole Genome Sequencing (WGS) — NeuraGenome
WGS sequences the entire genome — coding and non-coding regions — enabling detection of variants that panels and exome sequencing can miss, such as deep intronic changes, structural variants, and copy number variants. WGS is the most powerful genetic test when exhaustive genomic analysis is required.
When WGS is recommended
- Persistent diagnostic uncertainty despite prior panel or exome testing.
- Suspected structural genomic rearrangements or regulatory region defects.
- Complex phenotypes that require a comprehensive genomic approach.
Collection and processing
Careful sample collection and fast shipment preserve DNA integrity. Due to the depth of analysis, WGS reports include detailed interpretation and recommended clinical actions, often involving multidisciplinary review.