Turnaround Time
21-25 business days
Price
Inquire for pricing
Testing completed by
Gene by Gene
| Sample Requirements
myDNA will provide buccal (cheek) swab kits with each order.
Each test requires one buccal swab which are included in each kit. This is the preferred sample collection method.
myDNA will provide return packaging and a pre-paid shipping label.
*Shipping fees will apply.
If necessary, myDNA can accept most DNA sample types, including:
- Extracted DNA: 20ul of 50ng/ul, OD260/OD280 ~ 1.8, include details of extraction method with samples
- Blood: 3-5cc drawn in EDTA (purple-top) tube
| Shipping
- For blood samples, please ship at room temperature in an insulated container. IT’S IMPORTANT TO NOTE: DO NOT HEAT OR FREEZE SAMPLE
- For buccal swab please follow shipping information provided
| Testing Methodology
- Platform: Illumina NovaSeq 6000
- Results Delivery: Results are delivered to the customer via secure FTP transfer and are stored for 30-60 days
About Whole Genome Clinical Reporting
Whole Genome reporting is beneficial to understand a broad range of diseases and disease risk that may be of genetic origin. The myDNA report makes interpreting results easy so that clinicians can deliver meaningful results quicker. The report can be an effective test to identify the cause of the disease when clinicians are faced with a high degree of diagnostic uncertainty.
Benefits of Whole Genome Clinical Reports.
- Next Generation Sequencing (NGS) technology has become an invaluable method to support diagnosis of rare genetic conditions as well as to optimize an individual’s course of treatment for illness
- Whole genome sequencing (WGS) may be advantageous to whole exome sequencing (WES) as it is unbiased and evaluates both non-coding and coding regions of the genome
- WGS has the potential to identify single nucleotide variants (SNVs), small insertion/deletions (indels), copy number variants (CNVs) and structural variants (SVs) in both coding and non-coding regions
- WGS may be a follow up test should a WES test fail to identify the causative variant
Tests We Provide
Whole Exome Sequencing
Cardiovascular Panel
- Cardiovascular (174 Genes)
- Congenital Heart Defect (127 Genes)
- Cardiomyopathy (106 Genes)
- Aortopathy & Connective Tissue Disorders (56 Genes)
- Arrhythmia (40 Genes)
- Familial Hypercholesterolemia (6 Genes)
Oncology Panel
- Hereditary Cancer (113 Genes)
Other Panels
- Renal-Kidney (176 Genes)
- Immunodeficiency (Interpretation only) (50 Genes)
- Parkinson Alzheimer Dementia (47 Genes)
- RASopathies (26 Genes)
- Proactive Genetic Health Screen (311 Genes)
Custom reports are also available upon request. Enquire with our sales team for more information.
Inquire about Whole Genome Clinical Testing & Reporting Services Online
Submit the adjacent Test Request Form and our laboratory will be in touch to confirm your inquiry.
Note: For individuals interested in these services, please speak to your healthcare professional.