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1-84-
GENEHELP
(1-844-363-4357)
About Us
Contact Us
LifeLabs.com
Info en Français
Give us your Feedback
Our Tests
Reproductive Health
Non-Invasive Prenatal Testing
Non-Invasive Prenatal Testing French
Expanded Carrier Screening
Pharmacogenetics
TreatGx
Plus
Hereditary Cancers
Hereditary Cancer
Rare and Hereditary Conditions
Known Mutations and Single Genes
Multi-Gene Panel Testing
Whole Exome Sequencing
Whole Genome Sequencing
Search for a Test
Search for a Test
HealthCare Providers
HealthCare Providers
Forms & Requisitions
Search for a Test
How to Order
Physician Training and Research
Resources
PATIENTS
Genetic Counselling
Sample Collection
General FAQs
Links
HEALTHCARE PROVIDERS
Links
MEDIA
News & Events
Reproductive Health
Pharmacogenetics
Hereditary Cancers
Rare and Hereditary Conditions
Search for a Test
Non-Invasive Prenatal Testing
Panorama™ is a Non-Invasive Prenatal Test (NIPT) that screens for common genetic conditions caused by extra or missing chromosomes in the baby’s DNA as early as 9 weeks. Panorama analyzes baby's (placental) DNA through a simple blood draw from the mother’s arm.
NIPT/Cord Blood Banking Bundle
LifeLabs Genetics™, in collaboration with Insception Biosences, is offering a bundled package that includes Panorama NIPT and cord blood/tissue banking.
Expanded Carrier Screening
Expanded Carrier Screening identifies parents-to-be that are likely to pass on genetic conditions to their children. Even without a family history of disease, you can still be a carrier and benefit from this test, which screens for up to 288 conditions before or during pregnancy.
TreatGx
Plus
TreatGx
Plus
predicts your response to medications by analyzing medication-to-medication, medication-to-disease, and medication-to-genetic interactions. This personalized analysis leads to ideal medication and dosage options for you, so that safer and more effective medications can be prescribed
Hereditary Cancer
More and more Canadians with early cancer diagnoses or pronounced family histories of breast or ovarian cancers are considering BRCA1 and BRCA2 (BRCA1/2) genetic testing.
Known Mutations and Single Genes
These 3500+ diagnostic and predictive single gene and genetic panel tests provide concrete, actionable insights that lead to informed decision making and personalized treatment.
Multi-Gene Panel Testing
>200 panel options, spanning more than 15 medical specialties, to provide actionable insight and informed decision making
Whole Exome Sequencing
To determine a cause for a complex genetic disorder, Whole Exome Sequencing analyzes thousands of genes simultaneously, providing an alternative to single-gene tests or multigene panels, to investigate the molecular basis of genetic disorders.
Whole Genome Sequencing
WGS is one of the latest genetic technologies that sequences the entire coding and non-coding regions of the genome to help provide answers for individuals with complex disease where other tests have not.
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Hereditary Cancer
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