Services

Carrier Screening- 1200+ Panel, 1200+ Diseases Detected in 1 Test

 
Helping parents to detect genetic risks, provide reproductive guidance, and prevent birth defects.

Population who may need the test:
All couples who are planning a pregnancy or during early pregnancy, including those:
- With normal phenotypes and no family history of monogenic diseases.
- Who wants to have a healthy baby using assisted reproductive technology (ART).
- Who are close blood relatives.

Advantages:
• Reasonable disease selection
• Large database of mutations following ACMG guidelines
• Extensive experience in genetic disease screening and research
• Complete lab qualifications and quality certifications
• Genetic counseling expert team and online search tools

Technology:
Target area capture - high-throughput sequencing technology

Characteristics:
Rigorous: Inclusion of prenatal and early pregnancy diseases with clear pathogenic genes and severe and early onset diseases, following requirements of international guidelines.

Comprehensive: Detection of exon regions, splicing regions, some intron regions, promoter regions and UTR regions containing 1200+ target genes.

Accurate: Applying strict performance evaluation and quality control standards; pathogenicity of sites determined in strict accordance with ACMG guidelines.

Highly efficient: Screening of 1200+ autosomal recessive and X-linked single-gene diseases in 1 test, improving the comprehensive prevention and control of birth defects.

Price: RM2800

WITH FRAGILE-X SYNDROME (RM3080)
(WITH FXS) (WITH HEMOPHILIA A) (RM3480)