Preimplantation Genetic Testing for Aneuploidy
PGT-A with Structural Rearrangement Analysis and PN Check
Preimplantation Genetic Testing for Monogenic Disorders
Preimplantation Genetic Testing for Polygenic Disorders
Non-Invasive Prenatal Testing
Diagnostic prenatal testing via WES or WGS on amniotic fluid
Comprehensive Carrier Screening + Genetic Counseling
Comprehensive genetic screening for couples before marriage
Carrier screening for Fragile X syndrome
SMA carrier status detection via SMN1 copy number analysis
ISCN 2020 chromosome analysis by G-banding — prenatal, constitutional, and hematology-oncology
Hereditary heart condition screening
Hereditary neurological condition screening
Hereditary endocrine disorder screening
Inherited metabolic disorder screening
Hereditary skeletal condition screening
Hereditary eye condition screening
Hereditary hearing loss screening
Primary immunodeficiency screening
Hereditary blood disorder screening
Drug response genetic testing
Hereditary skin condition and melanoma risk screening
Genetic causes of hypogonadism
Genetic causes of infertility
Multi-cancer syndrome genetic screening covering 80+ genes
BRCA1/BRCA2 and 20+ related gene screening
Lynch syndrome, FAP, and related gene screening
Focused 52-gene hotspot panel targeting the most common actionable oncogene mutations
Expanded 161-gene panel with broader coverage, CNVs, and comprehensive fusion detection
Targeted somatic mutation profiling for solid tumors
Comprehensive tumor genomic profiling via tissue biopsy — powered by SOPHiA DDM™ analytics
Blood-based tumor genomic profiling via circulating tumor DNA — powered by SOPHiA DDM™ analytics
