{"product_id":"clinical-exome-sequencingces-mitochondrial-genome-sequencing_onco-with-mcc","title":"Clinical Exome Sequencing(CES) + Mitochondrial Genome Sequencing_ONCO With MCC","description":"\u003cp\u003eAmniotic Fluid\/ Chorionic Villus Sample\/Peripheral Venous Blood\/Cord blood,\/Extracted DNA\/Dry Blood Spot\/POC\u003c\/p\u003e\n\u003cdiv class=\"text-base my-auto mx-auto [--thread-content-margin:var(--thread-content-margin-xs,calc(var(--spacing)*4))] @w-sm\/main:[--thread-content-margin:var(--thread-content-margin-sm,calc(var(--spacing)*6))] @w-lg\/main:[--thread-content-margin:var(--thread-content-margin-lg,calc(var(--spacing)*16))] px-(--thread-content-margin)\"\u003e\n\u003cdiv class=\"[--thread-content-max-width:40rem] @w-lg\/main:[--thread-content-max-width:48rem] mx-auto max-w-(--thread-content-max-width) flex-1 group\/turn-messages focus-visible:outline-hidden relative flex w-full min-w-0 flex-col agent-turn\"\u003e\n\u003cdiv class=\"flex max-w-full flex-col gap-4 grow\"\u003e\n\u003cdiv data-message-author-role=\"assistant\" data-message-id=\"f283bcfb-00b3-43ee-a671-cef2e29f5dda\" dir=\"auto\" data-message-model-slug=\"gpt-5-5\" class=\"min-h-8 text-message relative flex w-full flex-col items-end gap-2 text-start break-words whitespace-normal outline-none keyboard-focused:focus-ring [.text-message+\u0026amp;]:mt-1\"\u003e\n\u003cdiv class=\"flex w-full flex-col gap-1 empty:hidden\"\u003e\n\u003cdiv class=\"markdown prose dark:prose-invert wrap-break-word w-full light markdown-new-styling\"\u003e\n\u003ch2 data-section-id=\"hcp666\" data-start=\"0\" data-end=\"82\"\u003eClinical Exome Sequencing (CES) + Mitochondrial Genome Sequencing_ONCO With MCC\u003c\/h2\u003e\n\u003ch3 data-section-id=\"jlj3sj\" data-start=\"84\" data-end=\"101\"\u003eTest Overview\u003c\/h3\u003e\n\u003cp data-start=\"102\" data-end=\"521\"\u003eClinical Exome Sequencing (CES) combined with Mitochondrial Genome Sequencing is an advanced genomic diagnostic test designed to identify disease-causing genetic variants associated with hereditary cancers, rare genetic disorders, and mitochondrial abnormalities. This comprehensive analysis evaluates thousands of clinically relevant genes along with the complete mitochondrial genome for accurate molecular diagnosis.\u003c\/p\u003e\n\u003ch3 data-section-id=\"iq7y2n\" data-start=\"523\" data-end=\"555\"\u003eWhy This Test is Recommended\u003c\/h3\u003e\n\u003cul data-start=\"556\" data-end=\"892\"\u003e\n\u003cli data-section-id=\"1m8aa6n\" data-start=\"556\" data-end=\"625\"\u003eDetects inherited genetic mutations linked to cancer predisposition\u003c\/li\u003e\n\u003cli data-section-id=\"7mqdv5\" data-start=\"626\" data-end=\"673\"\u003eIdentifies rare and complex genetic disorders\u003c\/li\u003e\n\u003cli data-section-id=\"zeg9zi\" data-start=\"674\" data-end=\"714\"\u003eEvaluates mitochondrial DNA variations\u003c\/li\u003e\n\u003cli data-section-id=\"24dmv1\" data-start=\"715\" data-end=\"775\"\u003eSupports precision medicine and targeted therapy decisions\u003c\/li\u003e\n\u003cli data-section-id=\"1c0bndr\" data-start=\"776\" data-end=\"832\"\u003eHelps in family risk assessment and genetic counseling\u003c\/li\u003e\n\u003cli data-section-id=\"1am8ce2\" data-start=\"833\" data-end=\"892\"\u003eUseful for unexplained syndromic or multisystem disorders\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"188ylwu\" data-start=\"894\" data-end=\"914\"\u003eWhat is Included\u003c\/h3\u003e\n\u003cul data-start=\"915\" data-end=\"1193\"\u003e\n\u003cli data-section-id=\"m9rxkv\" data-start=\"915\" data-end=\"988\"\u003eClinical Exome Sequencing (coding regions of clinically relevant genes)\u003c\/li\u003e\n\u003cli data-section-id=\"8uqo3b\" data-start=\"989\" data-end=\"1031\"\u003eComplete Mitochondrial Genome Sequencing\u003c\/li\u003e\n\u003cli data-section-id=\"1r36azg\" data-start=\"1032\" data-end=\"1076\"\u003eMCC (Maternal Cell Contamination) analysis\u003c\/li\u003e\n\u003cli data-section-id=\"13wuod7\" data-start=\"1077\" data-end=\"1108\"\u003eBioinformatics interpretation\u003c\/li\u003e\n\u003cli data-section-id=\"ed8if8\" data-start=\"1109\" data-end=\"1167\"\u003eVariant classification based on international guidelines\u003c\/li\u003e\n\u003cli data-section-id=\"1ums2c2\" data-start=\"1168\" data-end=\"1193\"\u003eDetailed genomic report\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"11twy89\" data-start=\"1195\" data-end=\"1214\"\u003eSample Required\u003c\/h3\u003e\n\u003cul data-start=\"1215\" data-end=\"1246\"\u003e\n\u003cli data-section-id=\"1fhinwf\" data-start=\"1215\" data-end=\"1246\"\u003ePeripheral Blood \/ EDTA Blood\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"1uvv5qj\" data-start=\"1248\" data-end=\"1263\"\u003eMethodology\u003c\/h3\u003e\n\u003cul data-start=\"1264\" data-end=\"1333\"\u003e\n\u003cli data-section-id=\"oumte0\" data-start=\"1264\" data-end=\"1298\"\u003eNext Generation Sequencing (NGS)\u003c\/li\u003e\n\u003cli data-section-id=\"17parst\" data-start=\"1299\" data-end=\"1333\"\u003eAdvanced Bioinformatics Analysis\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"ik3d6w\" data-start=\"1335\" data-end=\"1354\"\u003eRecommended For\u003c\/h3\u003e\n\u003cul data-start=\"1355\" data-end=\"1569\"\u003e\n\u003cli data-section-id=\"1xrhiyx\" data-start=\"1355\" data-end=\"1394\"\u003eSuspected hereditary cancer syndromes\u003c\/li\u003e\n\u003cli data-section-id=\"11uoqn9\" data-start=\"1395\" data-end=\"1433\"\u003eRare genetic and metabolic disorders\u003c\/li\u003e\n\u003cli data-section-id=\"iy0g4a\" data-start=\"1434\" data-end=\"1476\"\u003eNeuromuscular and mitochondrial diseases\u003c\/li\u003e\n\u003cli data-section-id=\"1vtulha\" data-start=\"1477\" data-end=\"1531\"\u003eDevelopmental delay or unexplained clinical symptoms\u003c\/li\u003e\n\u003cli data-section-id=\"sixw9t\" data-start=\"1532\" data-end=\"1569\"\u003eFamily history of genetic disorders\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"owkoul\" data-start=\"1571\" data-end=\"1590\"\u003eTurnaround Time\u003c\/h3\u003e\n\u003cul data-start=\"1591\" data-end=\"1616\"\u003e\n\u003cli data-section-id=\"1o5ktmb\" data-start=\"1591\" data-end=\"1616\"\u003eApproximately 4–6 Weeks\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"5y7puq\" data-start=\"1618\" data-end=\"1630\"\u003eBenefits\u003c\/h3\u003e\n\u003cul data-start=\"1631\" data-end=\"1819\"\u003e\n\u003cli data-section-id=\"3whr92\" data-start=\"1631\" data-end=\"1665\"\u003eComprehensive genomic evaluation\u003c\/li\u003e\n\u003cli data-section-id=\"wf6bq4\" data-start=\"1666\" data-end=\"1692\"\u003eHigh diagnostic accuracy\u003c\/li\u003e\n\u003cli data-section-id=\"i36ast\" data-start=\"1693\" data-end=\"1723\"\u003eEarly disease identification\u003c\/li\u003e\n\u003cli data-section-id=\"13twyll\" data-start=\"1724\" data-end=\"1765\"\u003eEnables personalized treatment planning\u003c\/li\u003e\n\u003cli data-section-id=\"9h7hqp\" data-start=\"1766\" data-end=\"1819\"\u003eSupports reproductive and family planning decisions\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3 data-section-id=\"1p5q70f\" data-start=\"1821\" data-end=\"1836\"\u003ePreparation\u003c\/h3\u003e\n\u003cp data-start=\"1837\" data-end=\"1904\"\u003eNo special preparation is required unless advised by the physician.\u003c\/p\u003e\n\u003ch3 data-section-id=\"7cj1qd\" data-start=\"1906\" data-end=\"1920\"\u003eDisclaimer\u003c\/h3\u003e\n\u003cp data-start=\"1921\" data-end=\"2052\"\u003eTest results should be interpreted by qualified healthcare professionals along with clinical history and other laboratory findings.\u003c\/p\u003e\n\u003cp data-start=\"2054\" data-end=\"2316\" data-is-last-node=\"\" data-is-only-node=\"\"\u003e#ClinicalExomeSequencing #MitochondrialGenomeSequencing #GeneticTesting #NGSTesting #OncologyDiagnostics #PrecisionMedicine #RareDiseaseDiagnosis #CancerGenetics #AdvancedBioCare #GenomicMedicine #MolecularDiagnostics #PersonalizedHealthcare #Dermafact #gynofact\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv class=\"z-0 flex min-h-[46px] justify-start\"\u003e\u003cbr\u003e\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e","brand":"Lifecell Diagnostics","offers":[{"title":"Default Title","offer_id":44007228866695,"sku":null,"price":15400.0,"currency_code":"INR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0691\/4241\/3447\/files\/46168f04-5b3e-4865-b4f7-1acdff0fc18c.png?v=1780043184","url":"https:\/\/ourdermastore.com\/products\/clinical-exome-sequencingces-mitochondrial-genome-sequencing_onco-with-mcc","provider":"Ourdermastore ","version":"1.0","type":"link"}