{"id":1962,"date":"2018-04-26T18:49:10","date_gmt":"2018-04-26T10:49:10","guid":{"rendered":"https:\/\/geniestgenomics.com\/?p=1962"},"modified":"2023-04-21T14:06:36","modified_gmt":"2023-04-21T06:06:36","slug":"180426","status":"publish","type":"post","link":"https:\/\/geniestgenomics.com\/index.php\/2018\/04\/26\/180426\/","title":{"rendered":"Rainbow Genomics\u5ba3\u4f48\u6574\u5408\u6d1b\u6749\u78ef\u52a0\u5dde\u5927\u5b78(UCLA)\u81e8\u5e8a\u57fa\u56e0\u7d44\u5b78\u4e2d\u5fc3\u7684\u81e8\u5e8a\u5206\u6790\u548c\u5831\u544a\u670d\u52d9\uff0c\u652f\u6301\u5168\u5916\u986f\u5b50\u7d44\u6e2c\u5e8f\u6aa2\u6e2c"},"content":{"rendered":"<h4>Rainbow Genomics<strong>\u5ba3\u4f48<\/strong>\u6574\u5408\u6d1b\u6749\u78ef\u52a0\u5dde\u5927\u5b78(UCLA)\u81e8\u5e8a\u57fa\u56e0\u7d44\u5b78\u4e2d\u5fc3\u7684\u81e8\u5e8a\u5206\u6790\u548c\u5831\u544a\u670d\u52d9, \u652f\u6301\u5168\u5916\u986f\u5b50\u7d44\u6e2c\u5e8f\u6aa2\u6e2c<\/h4>\n<h4>Rainbow Genomics Announces the Integration of Clinical Interpretation Services from the UCLA Clinical Genomics Center Supporting Whole Exome Sequencing Tests<\/h4>\n<ul data-rte-list=\"default\">\n<li>Rainbow Genomics\u6210\u529f\u6574\u5408\u6d1b\u6749\u78ef\u52a0\u5dde\u5927\u5b78\u81e8\u5e8a\u57fa\u56e0\u7d44\u5b78\u4e2d\u5fc3\u5206\u6790\u548c\u5831\u544a\u670d\u52d9, \u63d0\u4f9b\u5b8c\u6574\u7684\u5916\u986f\u5b50\u7d44\u6e2c\u5e8f\u6aa2\u6e2c\uff0c\u6db5\u84cb\u5927\u91cf\u7684\u6210\u4eba\u548c\u5152\u7ae5\u907a\u50b3\u75be\u75c5\u3002<\/li>\n<li>\u57fa\u65bc\u660e\u78ba\u91ab\u5b78\u8b49\u64da\u7684\u81e8\u5e8a\u5831\u544a\u5c07\u7531\u81e8\u5e8a\u57fa\u56e0\u7d44\u5b78\u4e2d\u5fc3\u7684\u57fa\u56e0\u7d44\u59d4\u54e1\u6703\u9032\u884c\u5be9\u67e5\u4e4b\u5f8c\u7c3d\u767c. \u9019\u500b\u59d4\u54e1\u6703\u662f\u7531\u4e00\u500b\u8de8\u5b78\u79d1\u7684\u5c08\u696d\u5718\u968a\u7d44\u6210, \u5176\u4e2d\u5305\u62ec\u91ab\u751f, \u5c08\u79d1\u91ab\u5e2b, \u81e8\u5e8a\u907a\u50b3\u5b78\u5bb6, \u751f\u7269\u4fe1\u606f\u5c08\u5bb6\u548c\u7814\u7a76\u6559\u6388, \u78ba\u4fdd\u5c0d\u6bcf\u4f4d\u60a3\u8005\u75be\u75c5\u60c5\u6cc1\u9032\u884c\u6700\u5168\u9762\u7684\u8a55\u4f30\u3002<\/li>\n<\/ul>\n<p>HONG KONG and SAN FRANCISCO (<a href=\"http:\/\/www.prweb.com\/releases\/2018\/04\/prweb15443294.htm\" target=\"_blank\" rel=\"noopener\">PRWEB<\/a>) April 26, 2018 &#8212; Hong Kong-based Rainbow Genomics<br \/>\nannounced the contracting of data analysis and clinical interpretation services with the UCLA Clinical<br \/>\nGenomics Center. This process is coupled with Rainbow Genomics\u2019 whole exome sequencing performed at its<br \/>\nCAP-accredited laboratory. The fully-integrated capabilities deliver whole exome sequencing tests covering<br \/>\ncardio, adult and pediatric genetic disorders. Clinical reports based on clear medical evidence will be issued by<br \/>\nU.S. board-certified medical directors at the UCLA Clinical Genomics Center.<\/p>\n<p>These tests are exome-sequencing-based, covering over 22,000 genes, which may increase diagnostic yields<br \/>\n(identifying the cause of a disorder), and cover Asian-specific genes that may not be included in many<br \/>\nmicroarray- or panel-based gene tests.<\/p>\n<p>Limited by traditional testing of only tens or even hundreds of genes at a time, many patients with suspected<br \/>\ngenetic disorders have suffered for years without obtaining a diagnosis, a frustrating process often described as<br \/>\na \u201cDiagnostic Odyssey\u201d. Whole exome sequencing is increasingly adopted by clinicians in the U.S. to quickly<br \/>\nobtain a diagnosis for these \u201cunresolved\u201d cases. With a diagnosis, physicians can predict the course of the<br \/>\ndisorder, provide a prognosis, and in certain cases, treat the disorder. The families, especially those with<br \/>\npediatric patients, can understand the genetic risks for other family members, and seek access to appropriate<br \/>\nsupport networks.<\/p>\n<p>UCLA Clinical Genomics Center is one of the first U.S. medical institutions offering clinical-grade whole<br \/>\nexome sequencing for diagnosis of pediatric and adult genetic disorders. Leveraging their extensive expertise in<br \/>\ndiagnosis and treatment of hereditary diseases, Rainbow Genomics is committed to helping Asian patients by<br \/>\nresolving their clinical cases. These undiagnosed cases, especially in the pediatric area, remain as a substantial<br \/>\nmedical burden for many local communities.<\/p>\n<p>\u201cThe UCLA Clinical Genomics Center is delighted to extend our services and expertise to the Asian<br \/>\npopulations served by Rainbow Genomics,&#8221; said Dr. Wayne Grody, Director of Molecular Diagnostics for the<br \/>\nUCLA Health system. \u201cWhile those countries have robust economies and impressive technology, they have<br \/>\nremained underserved in the areas of genetic testing and genomic medicine. This collaboration will go a long<br \/>\nway toward growing these services, with benefits on both sides of the Pacific.&#8221;<\/p>\n<p>\u201cRainbow Genomics is committed to bringing evidence-based genetic tests, supported by &#8216;actionable&#8217; findings,<br \/>\nto patients in Asia Pacific,\u201d Said Daniel Siu, CEO of Rainbow Genomics. \u201cCurrently, obtaining a whole exome<br \/>\nsequencing test from a leading U.S. medical institution without insurance coverage is prohibitively expensive.<br \/>\nThe relationship between UCLA Clinical Genomics Center and Rainbow Genomics enables many middle-class<br \/>\nfamilies to access exceptionally-high-quality exome sequencing genetic tests that may finally provide a<br \/>\ndiagnosis, something that these families have been seeking for years.&#8221;<\/p>\n<p><strong>About Rainbow Genomics<\/strong><br \/>\nRainbow Genomics is committed to providing clinically-validated and affordable genetic tests to patients in<br \/>\nHong Kong, Japan, Singapore and other Asian countries. The company delivers clinical interpretations<br \/>\nspecifically for Asians, based on expert understanding of their genetics, and medical care experience in Hong<br \/>\nKong, Japan, and the United States. Rainbow Genomics specializes in providing whole exome sequencing and<br \/>\npharmacogenomic tests to enable physicians to use genomic information for diagnosis, treatment, and disease<br \/>\nprevention. Visit us at rainbowgenomics.com.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Rainbow Genomics Announces the Integration of Clinical Interpretation Services from the UCLA Clinical Genomics Center Supporting Whole Exome Sequencing Tests<br \/>\nRainbow Genomics\u6210\u529f\u6574\u5408\u6d1b\u6749\u78ef\u52a0\u5dde\u5927\u5b78\u81e8\u5e8a\u57fa\u56e0\u7d44\u5b78\u4e2d\u5fc3\u5206\u6790\u548c\u5831\u544a\u670d\u52d9, \u63d0\u4f9b\u5b8c\u6574\u7684\u5916\u986f\u5b50\u7d44\u6e2c\u5e8f\u6aa2\u6e2c\uff0c\u6db5\u84cb\u5927\u91cf\u7684\u6210\u4eba\u548c\u5152\u7ae5\u907a\u50b3\u75be\u75c5\u3002<br \/>\n\u57fa\u65bc\u660e\u78ba\u91ab\u5b78\u8b49\u64da\u7684\u81e8\u5e8a\u5831\u544a\u5c07\u7531\u81e8\u5e8a\u57fa\u56e0\u7d44\u5b78\u4e2d\u5fc3\u7684\u57fa\u56e0\u7d44\u59d4\u54e1\u6703\u9032\u884c\u5be9\u67e5\u4e4b\u5f8c\u7c3d\u767c\uff0c\u9019\u500b\u59d4\u54e1\u6703\u662f\u7531\u4e00\u500b\u8de8\u5b78\u79d1\u7684\u5c08\u696d\u5718\u968a\u7d44\u6210\uff0c\u5176\u4e2d\u5305\u62ec\u91ab\u751f\u3001\u5c08\u79d1\u91ab\u5e2b\u3001\u81e8\u5e8a\u907a\u50b3\u5b78\u5bb6\u3001\u751f\u7269\u4fe1\u606f\u5c08\u5bb6\u548c\u7814\u7a76\u6559\u6388\uff0c\u78ba\u4fdd\u5c0d\u6bcf\u4f4d\u60a3\u8005\u75be\u75c5\u60c5\u6cc1\u9032\u884c\u6700\u5168\u9762\u7684\u8a55\u4f30\u3002 <\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[75],"tags":[],"class_list":["post-1962","post","type-post","status-publish","format-standard","hentry","category-75"],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/geniestgenomics.com\/index.php\/wp-json\/wp\/v2\/posts\/1962","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/geniestgenomics.com\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/geniestgenomics.com\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/geniestgenomics.com\/index.php\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/geniestgenomics.com\/index.php\/wp-json\/wp\/v2\/comments?post=1962"}],"version-history":[{"count":4,"href":"https:\/\/geniestgenomics.com\/index.php\/wp-json\/wp\/v2\/posts\/1962\/revisions"}],"predecessor-version":[{"id":1970,"href":"https:\/\/geniestgenomics.com\/index.php\/wp-json\/wp\/v2\/posts\/1962\/revisions\/1970"}],"wp:attachment":[{"href":"https:\/\/geniestgenomics.com\/index.php\/wp-json\/wp\/v2\/media?parent=1962"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/geniestgenomics.com\/index.php\/wp-json\/wp\/v2\/categories?post=1962"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/geniestgenomics.com\/index.php\/wp-json\/wp\/v2\/tags?post=1962"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}