{"product_id":"clinical-exome-sequencingces-80-100x-min-4-gb-data-raw-data-only","title":"Clinical Exome Sequencing(CES) 80-100X - Min 4 GB data- Raw Data Only","description":"\u003cp\u003eAmniotic Fluid\/ Chorionic Villus Sample\/Peripheral Venous Blood\/Cord blood,\/Extracted DNA\/Dry Blood Spot\u003c\/p\u003e\n\u003ch1 data-section-id=\"m7gm90\" data-start=\"0\" data-end=\"73\"\u003eClinical Exome Sequencing (CES) 80–100X – Min 4 GB Data – Raw Data Only\u003c\/h1\u003e\n\u003ch2 data-section-id=\"rzkdgm\" data-start=\"75\" data-end=\"86\"\u003eOverview\u003c\/h2\u003e\n\u003cp data-start=\"87\" data-end=\"420\"\u003eClinical Exome Sequencing (CES) is an advanced genetic test designed to analyze the protein-coding regions (exons) of thousands of genes associated with inherited disorders and genetic conditions. This test generates high-depth sequencing data with coverage of approximately 80–100X, ensuring accurate and reliable variant detection.\u003c\/p\u003e\n\u003cp data-start=\"422\" data-end=\"608\"\u003eThis package provides \u003cstrong data-start=\"444\" data-end=\"472\"\u003eraw sequencing data only\u003c\/strong\u003e with a minimum of \u003cstrong data-start=\"491\" data-end=\"511\"\u003e4 GB data output\u003c\/strong\u003e, suitable for research analysis, secondary bioinformatics interpretation, and archival purposes.\u003c\/p\u003e\n\u003chr data-start=\"610\" data-end=\"613\"\u003e\n\u003ch2 data-section-id=\"1hu7vo9\" data-start=\"615\" data-end=\"646\"\u003eWhat Does This Test Analyze?\u003c\/h2\u003e\n\u003cul data-start=\"647\" data-end=\"908\"\u003e\n\u003cli data-section-id=\"1i1pp2h\" data-start=\"647\" data-end=\"708\"\u003eProtein-coding regions (exons) of clinically relevant genes\u003c\/li\u003e\n\u003cli data-section-id=\"18ii93u\" data-start=\"709\" data-end=\"908\"\u003eGenetic variants associated with:\n\u003cul data-start=\"747\" data-end=\"908\"\u003e\n\u003cli data-section-id=\"tu0vp4\" data-start=\"747\" data-end=\"771\"\u003eRare genetic disorders\u003c\/li\u003e\n\u003cli data-section-id=\"5eipig\" data-start=\"774\" data-end=\"799\"\u003eNeurological conditions\u003c\/li\u003e\n\u003cli data-section-id=\"1fsejj5\" data-start=\"802\" data-end=\"822\"\u003eMetabolic diseases\u003c\/li\u003e\n\u003cli data-section-id=\"vk3qtx\" data-start=\"825\" data-end=\"850\"\u003eDevelopmental disorders\u003c\/li\u003e\n\u003cli data-section-id=\"1hav5wn\" data-start=\"853\" data-end=\"875\"\u003eHereditary syndromes\u003c\/li\u003e\n\u003cli data-section-id=\"ykmi\" data-start=\"878\" data-end=\"908\"\u003ePediatric genetic conditions\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003chr data-start=\"910\" data-end=\"913\"\u003e\n\u003ch2 data-section-id=\"1ma7m6t\" data-start=\"915\" data-end=\"930\"\u003eKey Features\u003c\/h2\u003e\n\u003cul data-start=\"931\" data-end=\"1188\"\u003e\n\u003cli data-section-id=\"1klolbu\" data-start=\"931\" data-end=\"976\"\u003eHigh-depth sequencing coverage: \u003cstrong data-start=\"965\" data-end=\"976\"\u003e80–100X\u003c\/strong\u003e\n\u003c\/li\u003e\n\u003cli data-section-id=\"1y2kgtd\" data-start=\"977\" data-end=\"1015\"\u003eMinimum \u003cstrong data-start=\"987\" data-end=\"1015\"\u003e4 GB raw sequencing data\u003c\/strong\u003e\n\u003c\/li\u003e\n\u003cli data-section-id=\"jeemgj\" data-start=\"1016\" data-end=\"1045\"\u003eRaw FASTQ\/BCL data delivery\u003c\/li\u003e\n\u003cli data-section-id=\"8g7j2s\" data-start=\"1046\" data-end=\"1102\"\u003eHigh-quality next-generation sequencing (NGS) platform\u003c\/li\u003e\n\u003cli data-section-id=\"12yn2vr\" data-start=\"1103\" data-end=\"1150\"\u003eSuitable for advanced bioinformatics analysis\u003c\/li\u003e\n\u003cli data-section-id=\"2lceb9\" data-start=\"1151\" data-end=\"1188\"\u003eComprehensive exon-level assessment\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003chr data-start=\"1190\" data-end=\"1193\"\u003e\n\u003ch2 data-section-id=\"1bcglrj\" data-start=\"1195\" data-end=\"1217\"\u003eSample Requirements\u003c\/h2\u003e\n\u003cul data-start=\"1218\" data-end=\"1289\"\u003e\n\u003cli data-section-id=\"1toef31\" data-start=\"1218\" data-end=\"1250\"\u003ePeripheral blood sample (EDTA)\u003c\/li\u003e\n\u003cli data-section-id=\"q4gr0q\" data-start=\"1251\" data-end=\"1289\"\u003eDNA extracted sample (if applicable)\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003chr data-start=\"1291\" data-end=\"1294\"\u003e\n\u003ch2 data-section-id=\"1ou2557\" data-start=\"1296\" data-end=\"1314\"\u003eRecommended For\u003c\/h2\u003e\n\u003cul data-start=\"1315\" data-end=\"1542\"\u003e\n\u003cli data-section-id=\"1rii45o\" data-start=\"1315\" data-end=\"1368\"\u003ePatients with suspected inherited genetic disorders\u003c\/li\u003e\n\u003cli data-section-id=\"n7cnpy\" data-start=\"1369\" data-end=\"1437\"\u003eIndividuals requiring comprehensive exome-level genetic evaluation\u003c\/li\u003e\n\u003cli data-section-id=\"1dfzmpi\" data-start=\"1438\" data-end=\"1479\"\u003eResearch and secondary genomic analysis\u003c\/li\u003e\n\u003cli data-section-id=\"1afi30s\" data-start=\"1480\" data-end=\"1542\"\u003eCases needing raw sequencing files for custom interpretation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003chr data-start=\"1544\" data-end=\"1547\"\u003e\n\u003ch2 data-section-id=\"jgpyzo\" data-start=\"1549\" data-end=\"1567\"\u003eTechnology Used\u003c\/h2\u003e\n\u003cul data-start=\"1568\" data-end=\"1676\"\u003e\n\u003cli data-section-id=\"jyz9r9\" data-start=\"1568\" data-end=\"1602\"\u003eNext-Generation Sequencing (NGS)\u003c\/li\u003e\n\u003cli data-section-id=\"sdr2nz\" data-start=\"1603\" data-end=\"1638\"\u003eClinical Exome Capture Technology\u003c\/li\u003e\n\u003cli data-section-id=\"1psfejo\" data-start=\"1639\" data-end=\"1676\"\u003eHigh-throughput sequencing platform\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003chr data-start=\"1678\" data-end=\"1681\"\u003e\n\u003ch2 data-section-id=\"1ko8sy6\" data-start=\"1683\" data-end=\"1701\"\u003eTurnaround Time\u003c\/h2\u003e\n\u003cp data-start=\"1702\" data-end=\"1746\"\u003eTypically \u003cstrong data-start=\"1712\" data-end=\"1725\"\u003e3–6 weeks\u003c\/strong\u003e from sample receipt.\u003c\/p\u003e\n\u003chr data-start=\"1748\" data-end=\"1751\"\u003e\n\u003ch2 data-section-id=\"1xccwmx\" data-start=\"1753\" data-end=\"1768\"\u003eDeliverables\u003c\/h2\u003e\n\u003cul data-start=\"1769\" data-end=\"1891\"\u003e\n\u003cli data-section-id=\"tx99or\" data-start=\"1769\" data-end=\"1846\"\u003eRaw sequencing data files only\n\u003cul data-start=\"1804\" data-end=\"1846\"\u003e\n\u003cli data-section-id=\"2bdxak\" data-start=\"1804\" data-end=\"1817\"\u003eFASTQ files\u003c\/li\u003e\n\u003cli data-section-id=\"1hulbsw\" data-start=\"1820\" data-end=\"1846\"\u003eMinimum 4 GB data output\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli data-section-id=\"jw40et\" data-start=\"1847\" data-end=\"1891\"\u003eNo clinical interpretation\/report included\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003chr data-start=\"1893\" data-end=\"1896\"\u003e\n\u003ch2 data-section-id=\"9ghvog\" data-start=\"1898\" data-end=\"1916\"\u003eImportant Notes\u003c\/h2\u003e\n\u003cul data-start=\"1917\" data-end=\"2156\"\u003e\n\u003cli data-section-id=\"1v75esr\" data-start=\"1917\" data-end=\"2083\"\u003eThis package includes \u003cstrong data-start=\"1941\" data-end=\"1958\"\u003eraw data only\u003c\/strong\u003e and does not include:\n\u003cul data-start=\"1983\" data-end=\"2083\"\u003e\n\u003cli data-section-id=\"1b3lkol\" data-start=\"1983\" data-end=\"2007\"\u003eVariant interpretation\u003c\/li\u003e\n\u003cli data-section-id=\"1qeybtr\" data-start=\"2010\" data-end=\"2032\"\u003eClinical correlation\u003c\/li\u003e\n\u003cli data-section-id=\"1h9rwdu\" data-start=\"2035\" data-end=\"2055\"\u003eGenetic counseling\u003c\/li\u003e\n\u003cli data-section-id=\"1dgh1pp\" data-start=\"2058\" data-end=\"2083\"\u003eFinal diagnostic report\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli data-section-id=\"1eq6t9a\" data-start=\"2084\" data-end=\"2156\"\u003eAdditional bioinformatics analysis may be required for interpretation.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003chr data-start=\"2158\" data-end=\"2161\"\u003e\n\u003ch2 data-section-id=\"g1fcsn\" data-start=\"2163\" data-end=\"2203\"\u003eBenefits of Clinical Exome Sequencing\u003c\/h2\u003e\n\u003cul data-start=\"2204\" data-end=\"2387\" data-is-only-node=\"\"\u003e\n\u003cli data-section-id=\"1gct9gr\" data-start=\"2204\" data-end=\"2228\"\u003eBroad genetic coverage\u003c\/li\u003e\n\u003cli data-section-id=\"8cr9qb\" data-start=\"2229\" data-end=\"2283\"\u003eHigh sensitivity for clinically significant variants\u003c\/li\u003e\n\u003cli data-section-id=\"mb52ct\" data-start=\"2284\" data-end=\"2329\"\u003eUseful in complex or undiagnosed conditions\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"Lifecell Diagnostics","offers":[{"title":"Default Title","offer_id":44007228899463,"sku":null,"price":9009.0,"currency_code":"INR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0691\/4241\/3447\/files\/4c3b1fcb-8f06-4a7c-be4e-1e0e5b9fba6c.png?v=1779872573","url":"https:\/\/ourdermastore.com\/products\/clinical-exome-sequencingces-80-100x-min-4-gb-data-raw-data-only","provider":"Ourdermastore ","version":"1.0","type":"link"}