import React from 'react';
import Image from 'next/image';
const FeatureCard = ({ icon, title, description }) => (
);
export default function OperifyExome() {
const features = [
{
title: "Deep Coverage",
desc: "≥100X average depth for high accuracy.",
icon: "/images/icons/deep-coverage.png"
},
{
title: "Superior Data Quality",
desc: "≥90% bases with Q30 score.",
icon: "/images/icons/data-quality.png"
},
{
title: "Comprehensive Variant Detection",
desc: "Identifies SNVs, Indels, and CNVs.",
icon: "/images/icons/variant-detection.png"
},
{
title: "Uniparental Disomy Analysis",
desc: "Detects UPD regions for imprinting disorders.",
icon: "/images/icons/upd-analysis.png"
},
{
title: "Coverage of Complex Genes",
desc: "Includes SMN1, SMN2, and DMD.",
icon: "/images/icons/complex-genes.png"
},
{
title: "Chromosomal Assessment",
desc: "Detects aneuploidies and determines chromosomal sex.",
icon: "/images/icons/chromosomal.png"
},
{
title: "Dynamic Reanalysis",
desc: "Reanalysis as scientific knowledge evolves.",
icon: "/images/icons/reanalysis.png"
}
];
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
{points.map((point, idx) => (
-
{point}
))}
Key Features
{features.map((feature, index) => (
))}
);
}