export default function OperifyExome() { const features = [ { title: "Deep Coverage", desc: "≥100X average depth for high accuracy." }, { title: "Superior Data Quality", desc: "≥90% bases with Q30 score." }, { title: "Comprehensive Variant Detection", desc: "Identifies SNVs, Indels, and CNVs." }, { title: "Uniparental Disomy Analysis", desc: "Detects UPD regions for imprinting disorders." }, { title: "Coverage of Complex Genes", desc: "Includes SMN1, SMN2, and DMD." }, { title: "Chromosomal Assessment", desc: "Detects aneuploidies and determines chromosomal sex." }, { title: "Dynamic Reanalysis", desc: "Reanalysis as scientific knowledge evolves." } ]; const points = [ "Whole Exome Sequencing (WES) targets the protein-coding regions of the genome, where most disease-causing mutations are found.", "With over 7,000 rare diseases identified—80% of which have a genetic basis—WES offers a powerful approach to uncover their causes.", "Traditional diagnostic methods can be slow, costly, and inconclusive; WES streamlines the process by delivering broad genetic insights in a single test.", "Operify Exome enhances WES by combining comprehensive coverage with advanced interpretation, improving diagnostic yield and patient outcomes." ]; return (

Operify Exome

Key Features

{features.map((feature, idx) => ( ))}
Feature Description
{feature.title} {feature.desc}
); }