Blended Genome Exome (BGE)
The Blended Low Pass 3X Genome + 40X Whole Exome (BGE) sequencing product combines the best of both worlds
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The Blended Low Pass 3X Genome + 40X Whole Exome (BGE) sequencing product combines the best of both worlds
Enquire OnlineUnbiased Discovery. Targeted Depth. The Blended Low Pass 3X Genome + 40X Whole Exome (BGE) sequencing product combines the best of both worlds. By integrating low-pass genome coverage with exome sequencing, we provide an ideal, budget-friendly solution for researchers and clinicians who require a holistic view of the genome without sacrificing precision in protein-coding regions.
- Whole Genome Insight: Analyze the entire genome at 3X coverage for structural variants and polygenic risk discovery.
- Exome Precision: Simultaneously perform a 40X coverage analysis of the most clinically relevant, protein-coding regions.
- Cost-Efficient: A robust alternative to high-depth Whole Genome Sequencing that maximizes data value per dollar.
Sample Requirements
Gene by Gene offers flexible intake options to accommodate various study designs and clinical needs. We accept:
- Gene by Gene Collection Kits: Optimized for our internal laboratory workflow.
- Pre-extracted DNA: Must be extracted in a CLIA-certified laboratory.
- External Collection Kits: Subject to approval by our laboratory team.
Results
We understand that data portability is essential for your pipeline. Gene by Gene provides seamless delivery of your raw data:
- File Formats: Industry-standard .cram or .fastq files.
- Delivery Methods: Secure transfer directly to the Client’s AWS S3 bucket or via sFTP.
Shipping
To ensure the highest quality sequencing results, please follow these stability guidelines:
- Blood Samples: Ship at room temperature in an insulated container.
- CRITICAL: Do not heat or freeze blood samples during transit.
- Buccal Swabs: Please follow the specific manufacturer’s instructions provided with the collection kit.
Testing Methodology
Technical Specifications
Genome Coverage: 3X Low-Pass
Exome Coverage: 40X
Methodology: Next-Generation Sequencing (NGS)
Data Outputs: .CRAM or .FASTQ
Turnaround Time: 10 – 15 business days
Turnaround Time
10-15 business days
Price
Inquire for pricing
Product Brochure
Submit the adjacent Test Request Form and our laboratory will be in touch to confirm your inquiry.