export default function OperifyExomeMito() { const features = [ { title: "High Mean Target Depth", desc: "≥100X coverage for reliable detection." }, { title: "High Base Quality", desc: "≥90% of bases with Q30 score." }, { title: "Scope of Test", desc: "Covers SNVs/Indels, CNVs in nuclear and mitochondrial genome." }, { title: "Uniparental Disomy", desc: "Detects regions important in rare recessive conditions." }, { title: "Homologous Gene Analysis", desc: "Includes SMN1, SMN2, DMD." }, { title: "Aneuploidy & Ploidy Estimation", desc: "Detects abnormal chromosome numbers and sex karyotype." }, { title: "Reanalysis & Reclassification", desc: "Updates based on latest scientific knowledge." } ]; const genomeCoverage = [ { genome: "Nuclear Genome", coverage: "Protein-coding regions of ~20000 genes" }, { genome: "Mitochondrial genome", coverage: "37 genes" } ]; const points = [ "The Operify ExomeMito Panel offers a unified solution by integrating whole exome sequencing with complete mitochondrial genome analysis—addressing both nuclear and mitochondrial causes of disease.", "This combined approach is especially valuable in diagnosing complex, multisystemic, and rare disorders, where variants may exist across both genomes.", "Mitochondrial disorders, though individually rare, are clinically significant, affecting approximately 1 in 5,000 individuals and often missed in standard testing.", "Studies show that adding mitochondrial sequencing to exome testing increases diagnostic yield by up to 20%, offering greater clarity and clinical confidence. (PMID: 30369941)", "While screening for rare genetic disorders, it's essential not to overlook the rarest among them-mitochondrial disorders, which occur in approximately 1 in 5,000 individuals. Although individually rare, their cumulative impact is significant in the context of rare disease diagnostics. Multiple studies have demonstrated a substantial increase in diagnostic yield—up to 20%—when mitochondrial genome sequencing is performed alongside whole exome sequencing. Reference: PMID: 30369941" ]; return (

Operify ExomeMito

Boost diagnostic yield with Exome + Mito Sequencing

Genome Coverage

{genomeCoverage.map((item, idx) => ( ))}
Genome Coverage
{item.genome} {item.coverage}

Key Features

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