{"id":3811,"date":"2023-09-02T22:25:28","date_gmt":"2023-09-02T14:25:28","guid":{"rendered":"https:\/\/www.igenehealth.com\/precision-prevention\/%e5%9f%ba%e5%9b%a0%e5%b8%b6%e5%9b%a0%e7%af%a9%e6%aa%a2\/"},"modified":"2024-10-26T20:53:59","modified_gmt":"2024-10-26T12:53:59","slug":"somatic-constitution-tracking-testing","status":"publish","type":"page","link":"https:\/\/www.cwintexmeds.com\/en\/cancer-constitution\/somatic-constitution-tracking-testing\/","title":{"rendered":"Somatic Constitution Tracking Testing"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-page\" data-elementor-id=\"3811\" class=\"elementor elementor-3811 elementor-3720\">\n\t\t\t\t\t\t<div class=\"elementor-inner\">\n\t\t\t\t<div class=\"elementor-section-wrap\">\n\t\t\t\t\t\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-63f97aa elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"63f97aa\" data-element_type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t\t\t<div class=\"elementor-row\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-92bbc64\" data-id=\"92bbc64\" data-element_type=\"column\">\n\t\t\t<div class=\"elementor-column-wrap elementor-element-populated\">\n\t\t\t\t\t\t\t<div class=\"elementor-widget-wrap\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-db2937d elementor-widget elementor-widget-text-editor\" data-id=\"db2937d\" data-element_type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-text-editor elementor-clearfix\">\n\t\t\t\t<div><div><div><div><div><div><div><div dir=\"ltr\"><h2 data-sourcepos=\"1:1-1:321\">Testing Specifications<\/h2><h2 data-sourcepos=\"1:1-1:321\">\u2022Sequencing Method: RNA-Seq 30M<\/h2><h2 data-sourcepos=\"1:1-1:321\">\u2022Bioinformatics Analysis: Hardware-accelerated analysis in Taiwan<\/h2><h2 data-sourcepos=\"1:1-1:321\">\u2022Interpretation Report: Constitution Tracking Interpretation Report<\/h2><p data-sourcepos=\"31:1-31:249\">\u00a0<\/p><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div>\t\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 class=\"elementor-element elementor-element-0d93df6 elementor-widget elementor-widget-text-editor\" data-id=\"0d93df6\" data-element_type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-text-editor elementor-clearfix\">\n\t\t\t\t<div><div><div><div><div><div><div><div dir=\"ltr\"><h2 data-sourcepos=\"1:1-1:321\">Scope of Application<\/h2><h2 data-sourcepos=\"1:1-1:321\">1.Cases where only cancer genome sequencing was previously conducted but treatment outcomes were suboptimal.<\/h2><h2 data-sourcepos=\"1:1-1:321\">2.Patients seeking a more comprehensive understanding of their cancer genomic changes to explore new treatment strategies for improved effectiveness.<\/h2><h2 data-sourcepos=\"1:1-1:321\">3.Cancer patients interested in enhancing their treatment with herbal medicine.<\/h2><p data-sourcepos=\"31:1-31:249\">\u00a0<\/p><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div>\t\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 class=\"elementor-element elementor-element-1f07e40 elementor-widget elementor-widget-text-editor\" data-id=\"1f07e40\" data-element_type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t<div class=\"elementor-text-editor elementor-clearfix\">\n\t\t\t\t<div>\n<div>\n<div>\n<div>\n<div>\n<div>\n<div>\n<div dir=\"ltr\">\n<h2 data-sourcepos=\"1:1-1:321\">Testing Purpose<\/h2><h2 data-sourcepos=\"1:1-1:321\">By sequencing the cancer transcriptome (or expression profile), this analysis reveals differences in genomic function between cancer and normal cells, identifying cancer-specific gene expressions, unique RNA splicing events, cancer-specific fusion genes, cancer-associated microorganisms, and changes within the tumor microenvironment. These insights are critical to patient treatment outcomes and survival. Our company uses RNA sequencing of both cancer tissues and surrounding normal tissues to identify unique cancer-related variations in individual cases. We then compare these findings with key cancer databases, such as the U.S. \u201cCancer Genome Atlas,\u201d to identify survival-related genes. Leveraging our proprietary methods, we consult our herbal medicine database to identify herbal treatments that target these genes, providing tailored options for clinical use.<\/h2><h2 data-sourcepos=\"1:1-1:321\"><br><\/h2><h2 data-sourcepos=\"1:1-1:321\">In addition, transcriptome sequencing analyzes the real-time functional changes in the cancer genome, reflecting immediate shifts in constitution. Detailed transcriptome analysis not only determines if genomic functions are operating correctly but also tracks the effects of environmental changes, diet, or personal lifestyle habits on genomic function. The results support precise personalized constitution management, including tailored herbal constitution adjustments.<\/h2>\n<p data-sourcepos=\"31:1-31:249\">\n<\/p><\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>Testing Specifications \u2022Sequencing Method: RNA-Seq 30M \u2022Bioinformatics Analysis: Hardware-accelerated analysis in Taiwan \u2022Interpretation Report: Constitution Tracking Interpretation Report \u00a0 Scope of Application 1.Cases where only cancer genome sequencing was previously conducted but treatment outcomes were suboptimal. 2.Patients seeking a more comprehensive understanding of their cancer genomic changes to explore new treatment strategies for improved effectiveness. 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