Services

Next Generation Sequencing (NGS) is the latest sequencing technique for analyzing genetic changes related to genetic diseases, which enables the analysis of a large number of genes either as a panel or as single genes.

The Only Available Method for Identifying Single-Gene Disorders in Embryos Before IVF and Pregnancy

Rapid Analysis of Trisomies 13, 18, 21 and Sex Chromosomes X and Y as the Most Common Chromosomal Abnormalities During Pregnancy

Analysis of One of the Most Common Genetic Diseases in Iran

Spinal Muscular Atrophy, a Hereditary Neuromuscular Disease

Analysis of 37 Genes Related to Hereditary Cancers of Breast, Ovary, Uterus, Prostate, Stomach, Intestine, Pancreas, and Skin using NGS Method

Special Panel for Carrier Status Determination in 433 Genes with Genetic Changes Analysis in Fragile X, SMA, and Duchenne Diseases

Analysis of Genes Contributing to Celiac Disease

Genetic Testing for FMF Disease Risk

Analysis of Genes and Changes Affecting Diagnosis and Treatment of Blood Cancers

Analysis of Genes Affecting Targeted Therapy in Lung Cancer Patients

Chromosomal Abnormalities Diagnosis in Potential Blood Malignancy Cases

Prenatal Chromosomal Abnormalities Diagnosis

Chromosomal Abnormalities Diagnosis in Men and Women