Rapid exome service
XOME Express (Trio)
Genetic exome sequencing for fast identification of top variants using BGI's automated variant analysis pipeline.
TAT15 working days
View detailsGeneticlab × BGI partnership
Precision genetic testing for complex clinical decisions.
XOME gives clinicians, hospitals, geneticists, and families a clear pathway into targeted panels, exome sequencing, whole genome testing, and validation workflows with clinically structured reporting and practical turnaround times.
15–35 days
TAT range
20,000+
Genes covered
4,800+ known genes
Disease focus
Individual + Trio
Testing modes
Rare disease workups
Trio-ready analysis
Turnaround-led pathways
Our tests
A complete XOME testing portfolio built for real clinical decision-making.
From focused validation services to whole exome and clinical whole genome testing, XOME supports multiple entry points depending on phenotype clarity, family history, turnaround needs, and diagnostic complexity.
Exome & Genome
Broad-coverage sequencing for rare disease and complex cases.
Monogenic Disease Panels
Targeted gene testing for suspected monogenic conditions.
Validation Services
Add-on confirmation for variants and copy-number changes.
Featured pathways
Highlighted testing options
Comprehensive exome
Whole Exome Sequencing (cWES Trio)
Whole exome sequencing across 180,000+ exons and 22,000 genes for rare genetic disorders and unclear clinical genotypes.
TAT25 working days
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Focused monogenic panel
Monogenic Disease Testing (1–9 genes)
Targeted sequencing for monogenic disease assessment with clinically directed scope for patients or families with a strong suspected diagnosis.
TAT25 working days
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Expanded monogenic panel
Monogenic Disease Testing (200+ genes)
Targeted sequencing of over 5,000 disease types across 10 body systems in conjunction with clinical presentation and disease progression markers.
TAT25 working days
View detailsTechnology coverage
Designed to support both high-level consultation and deeper technical review.
The XOME portfolio spans targeted panels, exome, and whole genome strategies with clinically relevant variant classes and family-based interpretation options where needed.
SNV and InDel detection
Exon-level and chromosome-level CNV
Mitochondrial genome analysis
Deep intron review where applicable
Structural variation and loss of heterozygosity
Dynamic mutation support in selected workflows
Clinical workflow
A clear path from counselling to reporting.
The website is built for clinicians and institutions that need clarity fast, while still being understandable for patients and families reviewing their options.
Step 1
Genetic counselling
Step 2
Sample collection
Step 3
Shipment
Step 4
DNA extraction and quality control
Step 5
Sequencing
Step 6
Data analysis
Step 7
Report delivery
Step 8
Translation and counselling
A trusted collaboration
Why this partnership
Local access through Geneticlab, advanced genomic capability through BGI.
XOME is presented as a clinical partnership rather than a generic brochure, making the collaboration visible in the first viewport and reinforcing trust throughout the site.
Co-branded delivery model combining Geneticlab's local clinical access with BGI's sequencing infrastructure
Testing options spanning targeted panels, validation services, exome, and whole genome
Trio workflows available where family-based interpretation improves clinical clarity
Turnaround-conscious packages for time-sensitive institutions and high-throughput settings
Speak with the team
Get the right XOME pathway for your patient, family, or service line.
Call geneticlab directly for service access, logistics, and next-step guidance.