{"id":11146,"date":"2024-01-01T22:08:17","date_gmt":"2024-01-01T21:08:17","guid":{"rendered":"https:\/\/www.arcensus-diagnostics.com\/?page_id=11146"},"modified":"2025-07-15T16:09:32","modified_gmt":"2025-07-15T14:09:32","slug":"products","status":"publish","type":"page","link":"https:\/\/www.arcensus-diagnostics.com\/en\/products\/","title":{"rendered":"Products"},"content":{"rendered":"\t\t
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Delivering Genomic Insights<\/h1>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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\n\t\t\t\t\t\t\t\t\tOur Products\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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For Physicians<\/h5>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Whole Genome Sequencing<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Maximise clinical utility in genetic testing<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\tmyLifeGenome \u00bb<\/span>\n\t\t\t\t\t<\/span>\n\t\t\t\t\t<\/a>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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For Physicians<\/h5>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Whole Exome Sequencing<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Unlock genetic insights at a lower cost<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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For Laboratories<\/h5>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Raw Data Interpretation<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Leverage sophisticated bioinformatics<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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Variant categories detected in nuclear and mitochondrial genomes<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Variant Type<\/th>Definition<\/th>WES<\/th>WGS<\/th><\/tr><\/thead>
Single nucleotide variants (SNVs)<\/td>A DNA sequence variant affecting 1 nucleotide<\/td>All protein-coding<\/td>All<\/td><\/tr>
Insertion \/ Deletion (Indels)<\/td>Deletions, insertions, or duplications of DNA segments less than 500bp<\/td>All protein-coding<\/td>All<\/td><\/tr>
Copy number variants (CNVs)<\/td>Deletions or duplications of DNA segments of at least 500bp<\/td>Limited<\/td>All<\/td><\/tr>
Structural variants (SVs)<\/td>Insertions of DNA segments of at least 500bp, inversions and translocations (including translocations between nDNA and mtDNA)<\/td>Limited<\/td>All<\/td><\/tr>
Repeat expansions<\/td>Increase in the number of repeated DNA sequence motifs within a gene<\/td>No<\/td>Most<\/td><\/tr>
Chromosomal abnormalities<\/td>Monosomy, trisomy, uniparental disomy, triploidy<\/td>All<\/td>All<\/td><\/tr><\/tbody><\/table>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Increase the Chances<\/h5>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Stay ahead in a rapidly evolving space<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Re-evaluation: <\/strong>As scientific knowledge advances, new disease-causing variants are discovered. At Arcensus, we re-evaluate all myLifeExome and myLifeGenome data twice within 12 months after the initial analysis. By conducting repeated analysis, we enhance the likelihood of identifying clinically significant variants and the root cause of genetic diseases.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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1st Analysis
<\/b>TAT: 20 working days<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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2nd Analysis
<\/b>within 6 months<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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3rd Analysis
<\/b>within 12 months<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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Re-classification: <\/strong>When any reported variant is re-classified, all impacted patients receive an updated report.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Contact us<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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We can help. Our team of experts is on hand to answer your questions.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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\n\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\tGet in touch<\/span>\n\t\t\t\t\t<\/span>\n\t\t\t\t\t<\/a>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"

Delivering Genomic Insights For Physicians Whole Genome Sequencing Maximise clinical utility in genetic testing myLifeGenome \u00bb For Physicians Whole Exome Sequencing Unlock genetic insights at a lower cost myLifeExome \u00bb For Laboratories Raw Data Interpretation Leverage sophisticated bioinformatics Data2Report \u00bb Variant categories detected in nuclear and mitochondrial genomes Variant Type Definition WES WGS Single nucleotide […]<\/p>\n","protected":false},"author":2,"featured_media":10879,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"elementor_header_footer","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-11146","page","type-page","status-publish","has-post-thumbnail","hentry"],"acf":[],"yoast_head":"\nArcensus – Products<\/title>\n<meta name=\"description\" content=\"Explore Arcensus' products including Whole Genome Sequencing, Whole Exome Sequencing, and Raw Data interpretation. 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