PGT-A (Aneuploidy):

Previously known as PGS, testing to determine if the correct chromosome number is in the embryo (explained here).

By combining copy number and genotyping data, LifeView provides the most accurate and highest resolution prediction of chromosomal abnormalities in the industry.  Fewer false positives means more embryos available for transfer.

PGT-SR (Structural Rearrangement):

Sometimes known as chromosomal PGD, testing for translocations and inversions.

LifeView PGT-SR provides more than 5 times the resolution of NGS based testing and the ability to distinguish between balanced translocation carrier and truly normal embryos for our patients.

PGT-M (Monogenic Disorders):

Sometimes known as PGD, testing for all single-gene disorders when there is a family history.

⦿ Cystic Fibrosis
⦿ Thalassemia
⦿ Huntington's disease
⦿ Our test is universal, covering all known monogenic diseases.

Copies of previous genetic testing results are required. Saliva samples from other family members may be required. Our genetic counselor and laboratory director will review your case and determine if testing is possible.

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Rapid workups and broader accommodation of difficult cases means faster time to pregnancy for prospective patients.

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By combining linkage-based analysis of several hundred markers with direct testing of the mutation, LifeView PGT-M provides the most convenient, cost effective, and accurate method available.

PGT-P (Polygenic Disorders):

⦿ Type 1 and Type 2 Diabetes
⦿ Breast Cancer, Testicular Cancer, Prostate Cancer, Malignant Melanoma, Basal Cell Carcinoma
⦿ Coronary Artery Disease, Heart Attack, Hypercholesterolemia, Hypertension
⦿ Schizophrenia

Send us an email requesting to become a provider, at service@gpclaboratory.com.

PGT-A (Aneuploidy):

Our position on the ethics, efficacy, and science of PGT-A: