{"id":130010,"date":"2023-12-19T16:28:57","date_gmt":"2023-12-19T05:28:57","guid":{"rendered":"https:\/\/www.mydna.life\/?page_id=130010"},"modified":"2025-01-16T15:05:11","modified_gmt":"2025-01-16T23:05:11","slug":"whole-genome-sequencing","status":"publish","type":"page","link":"https:\/\/www.mydna.life\/en-us\/whole-genome-sequencing\/","title":{"rendered":"Whole Genome Sequencing"},"content":{"rendered":"

[vc_row css=”.vc_custom_1702945561061{padding-top: 10vh !important;}”][vc_column width=”1\/6″][vc_column_text]Turnaround Time<\/p>\n

21-25 business days<\/strong>[\/vc_column_text][\/vc_column][vc_column width=”1\/6″][vc_column_text]Price<\/p>\n

Inquire for pricing<\/strong>[\/vc_column_text][\/vc_column][vc_column width=”1\/6″][vc_column_text]Testing completed by<\/p>\n

Gene by Gene<\/strong>[\/vc_column_text][\/vc_column][vc_column width=”1\/6″][\/vc_column][vc_column width=”1\/6″][\/vc_column][vc_column width=”1\/6″][\/vc_column][\/vc_row][vc_row css=”.vc_custom_1702945023379{padding-top: 5vh !important;padding-bottom: 1vh !important;}”][vc_column width=”1\/2″][vc_tta_tabs active_section=”1″][vc_tta_section title=”Requirements” tab_id=”1702944281951-8a02fdf3-644c”][vc_column_text css_animation=”fadeIn” css=”.vc_custom_1709594407092{padding-top: 20px !important;padding-bottom: 20px !important;}”]<\/p>\n

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| <\/strong>Sample Requirements<\/strong><\/h6>\n

myDNA will provide buccal (cheek) swab kits with each order.<\/p>\n

Each test requires one buccal swab which are included in each kit. This is the preferred sample collection method.<\/p>\n

myDNA will provide return packaging and a pre-paid shipping label.
\n*Shipping fees will apply.<\/sup><\/p>\n

If necessary, myDNA can accept most DNA sample types, including:<\/p>\n

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  • Extracted DNA: 20ul of 50ng\/ul, OD260\/OD280 ~ 1.8, include details of extraction method with samples<\/li>\n
  • Blood: 3-5cc drawn in EDTA (purple-top) tube<\/li>\n<\/ul>\n<\/div>\n

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    | <\/strong>Shipping<\/strong><\/h6>\n
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    • For blood samples, please ship at room temperature in an insulated container. IT\u2019S IMPORTANT TO NOTE:\u00a0DO NOT HEAT OR FREEZE SAMPLE<\/strong><\/li>\n
    • For buccal swab please follow shipping information provided<\/li>\n<\/ul>\n<\/div>\n

      [\/vc_column_text][\/vc_tta_section][vc_tta_section title=”Methodology” tab_id=”1702944285434-782f6740-ca7a”][vc_column_text css_animation=”fadeIn” css=”.vc_custom_1702953055300{padding-top: 20px !important;padding-bottom: 20px !important;}”]<\/p>\n

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      | <\/strong>Testing Methodology<\/strong><\/h6>\n
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      • Platform<\/strong>: Illumina NovaSeq 6000<\/li>\n
      • Results Delivery<\/strong>: Results are delivered to the customer via secure FTP transfer and are stored for 30-60 days<\/li>\n<\/ul>\n<\/div>\n

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        About Whole Genome<\/span> Clinical Reporting<\/h3>\n

        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.<\/p>\n

        Benefits of Whole Genome Clinical Reports.<\/strong><\/p>\n

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        • Next Generation Sequencing (NGS) technology has become an invaluable method to support diagnosis of rare genetic conditions as well as to optimize an individual\u2019s course of treatment for illness<\/li>\n
        • Whole genome sequencing (WGS)\u00a0 may be advantageous to whole exome sequencing (WES) as it is unbiased and evaluates both non-coding and coding regions of the genome<\/li>\n
        • 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<\/li>\n
        • WGS may be a follow up test should a WES test fail to identify the causative variant<\/li>\n<\/ul>\n<\/div>\n

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          Tests We Provide<\/span><\/h3>\n

          Whole Exome Sequencing<\/strong><\/p>\n

          Cardiovascular Panel<\/strong><\/p>\n

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          • Cardiovascular<\/strong> (174 Genes)<\/li>\n
          • Congenital Heart Defect<\/strong>\u00a0(127 Genes)<\/li>\n
          • Cardiomyopathy<\/strong>\u00a0(106 Genes)<\/li>\n
          • Aortopathy & Connective Tissue Disorders<\/strong>\u00a0(56 Genes)<\/li>\n
          • Arrhythmia <\/strong>(40 Genes)<\/li>\n
          • Familial Hypercholesterolemia<\/strong>\u00a0(6 Genes)<\/li>\n<\/ul>\n

            Oncology Panel<\/strong><\/p>\n

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            • Hereditary Cancer <\/strong>(113 Genes)<\/li>\n<\/ul>\n

              Other Panels<\/strong><\/p>\n

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              • Renal-Kidney <\/strong>(176 Genes)<\/li>\n
              • Immunodeficiency (Interpretation only)<\/strong>\u00a0(50 Genes)<\/li>\n
              • Parkinson Alzheimer Dementia<\/strong>\u00a0(47 Genes)<\/li>\n
              • RASopathies <\/strong>(26 Genes)<\/li>\n
              • Proactive Genetic Health Screen<\/strong> (311 Genes)<\/li>\n<\/ul>\n

                Custom reports are also available upon request. Enquire with our sales team for more information.<\/p>\n<\/div>\n

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                Inquire about Whole Genome Clinical Testing & Reporting <\/span>Services Online<\/h3>\n

                Submit the adjacent Test Request Form and our laboratory will be in touch to confirm your inquiry.<\/p>\n

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