Genomic Screening Tests
The Genomic Screening tests incorporate the power of genome sequencing with rigorous clinical interpretation of sequence information. The Genomic Screening tests will provide physicians with unparalleled interpretation of genomic data. Read more details about this test.
Requisition Form
All samples must be accompanied with a completed requisition form. Please make sure any identifiers used on the specimen are provided on the paperwork. Consent page should be signed by a health care provider. Any incomplete or missing paperwork may delay the start of testing.
Test Detail
Ordering
| Genome Screening - lmWGS-pnlE_L |
| Expanded Genome Screening - lmWGS-pnlF_L* |
|
Sequence Confirmation Test (V2) - lmSeqConV2_L |
| *Additional codes used with Expanded Genome Screening and Reflex to Expanded Genomic Screening. |
| Pharmacogenomics Panel (199 Variants) - lmPGX-pnlB_L |
| Risk Allele Panel A (22 Variants) - lmRISK-pnlBv2_L |
Reporting Genome Sequencing is anticipated to be about 12-16 weeks, but may vary depending upon the complexity of the case and the volume of cases within the laboratory. Please contact us for current turn-around times.
Preferred sample(s):
4-8 ml of whole blood collected in a lavender (K2EDTA/K3EDTA) top tube
OR
DNA sample: 5–10 µg extracted DNA at a concentration of 50 ng/µl in Tris-EDTA (TE) buffer with OD260/280 between 1.8-2.0.
Billing Information
The Laboratory for Molecular Medicine offers several billing options for our clients and their patients; however, we do not bill insurance companies and are unable to begin testing without accurate billing information.
Genomic Screening - $1,900
Expanded Genomic Screening - $2,950
For questions, please contact us at 617-768-8500 or by email.
