Whole Genome Testing Packages
Whole Genome Sequencing (WGS) reads across your genome to identify genetic variants that may be relevant to health risk, inherited conditions, and carrier status. Each package includes a clear genetic report, with optional access to your underlying sequencing files.
 
Whole Genome Basic Package
Best for proactive screening and general insights.
 
What it includes
WGS with an individual genetic report
Screening focused on common U.S./European variants and associated conditions
Coverage of roughly 200 conditions (screening-level)
 
Best for
Individuals who want a practical baseline view of inherited risk without a specific condition driving the analysis
 
Whole Genome Panel Plus Package
Recommended when a condition is involved or you want deeper, targeted interpretation.
 
What it includes
Everything in Whole Genome Basic, plus:
In-depth analysis of up to 3 conditions (based on symptoms, personal/family history, or areas of concern)
Interpretation supported by major national/reference resources such as ClinVar, OMIM, ClinGen, gnomAD, dbSNP, and other widely used genomic knowledge sources
 
Best for
Individuals or families with a known or suspected condition, unexplained symptoms, or a strong family history who want deeper condition-focused evaluation
 
Whole Genome Executive Package
Best for the most comprehensive pathogenic-variant and carrier-status screening.
 
What it includes
Comprehensive review of pathogenic/likely pathogenic classified variants across available databases
Carrier status screening for inherited conditions
Expanded screening scope intended to capture the broadest set of clinically relevant findings available through this analysis
 
Best for
Those who want the widest screening scope and the most comprehensive pathogenic + carrier review
 
Included with all packages
Genetic report with a clear, easy-to-understand summary of findings
Access to raw data files when requested (FASTQ, BAM, VCF)
Secure handling of genomic data with the option for future reanalysis as scientific knowledge evolves
 
Important notes (limitations)
Whole genome sequencing can identify many—though not all—types of genetic variation, and interpretation depends on the current state of scientific evidence. Results are not intended to diagnose or rule out disease and may require clinical confirmation and/or discussion with a qualified healthcare professional.