Whole Genome sequencing (Trio)

Whole Genome Sequencing (Trio)🧬

Whole Genome Sequencing (Trio) is an advanced genetic test that analyzes the complete DNA sequence of three individuals—typically a child and both biological parents. This comprehensive approach helps identify inherited genetic variants and understand how specific genetic changes are passed within a family.

This test is especially useful for diagnosing rare genetic disorders, developmental delays, congenital anomalies, and unexplained medical conditions. By comparing the genomes of the child with both parents, scientists can accurately detect de novo mutations, inherited variants, and disease-causing genetic alterations.

At Advanced BioCare Laboratories, Whole Genome Sequencing (Trio) uses state-of-the-art next-generation sequencing (NGS) technology to provide high-resolution genomic analysis and clinically actionable insights. The test supports early diagnosis, personalized treatment planning, and informed genetic counseling for families.

Key Features

🔬 Complete analysis of the entire genome
👨👩👧 Trio analysis (Child + Parents) for higher diagnostic accuracy
🧬 Detects inherited and new genetic mutations
📊 Supports diagnosis of rare and complex genetic disorders
⚕️ Helps guide personalized treatment and genetic counseling

Recommended For

• Children with unexplained developmental delay
• Suspected genetic or inherited disorders
• Rare disease diagnosis
• Families seeking genetic risk assessment

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