PGTseq-M, available only through Juno Genetics, is a unique test customized for each family. With PGTseq-M, Juno Genetics can detect genetic alterations associated with specific single gene disorders in an embryo prior to transfer during an in vitro fertilization (IVF) cycle.
Customized Single Gene Disorder Testing
PGTseq-M, available only through Juno Genteics is a unique test customized for each family. With PGTseq-M, Juno Genetics can detect genetic alterations associated with specific single gene disorders in an embryo prior to transfer during an in vitro fertilization (IVF) cycle.
A test as unique as your genetics
A single gene disorder is a disease that is caused by a known alteration or variant in one of the more than 20,000 genes in nearly every cell of the body. A disorder may be passed down in a family or inherited from both members of a couple who are carriers of the same condition.
PGTseq-M is customized to identify the specific disorder(s) of interest in your embryos. By transferring only embryos that do not have the associated genetic alteration(s) or variant(s), families decrease their risk of having a child with that single gene disorder(s). All embryos tested with PGTseq-M will also receive aneuploidy screening with PGTseq-A.
Juno Genetics can accurately test for nearly all single gene disorders, giving you peace of mind as you grow your family.
Review genetic test results
Collect samples
Develop custom test
Completion of probe development
Receive embryo biopsy samples
Analyze DNA
Report sent to your clinical team
Schedule IVF transfer
Talk to your doctor, nurse, or genetic counselor about PGTseq-M and the specific single gene disorder for which you may consider testing.
