Test Code: WESTRP

Whole Exome Sequencing (WES) - TRIO - Prenatal

Rare Diseases
Prenatal trio sequencing using fetal DNA (e.g., amniotic fluid or CVS) alongside parental samples. Enables early detection of clinically significant variants, guiding pregnancy management and genetic counseling.
Coverage: Whole exome regions (~20,000 genes), mitochondrial genome (chrM), and CNV spike‑in probes

Sample Type
Peripheral Blood in EDTA
Turnaround Time
21 -28 days
Courier Requirements
Ship overnight at room temperature to receive next day. Do not refrigerate or freeze. Maintain specimen at room temperature.
Pricing

Methodology

Next Generation Sequencing

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