Also 醫學KOL:「只有少少口水,檢測怎可能測到你DNA呢?怎可能測到你器官捐贈的匹配度(HLA type)呢?」
CircleDNA即是Prenetics,即是林鄭最初點名的武漢病毒檢測公司。講到明用一滴口水做「全外顯子測序」(whole exome sequencing),測你器官匹配度、隱病暗病、家族譜系,綽綽有餘。
很落力賣廣告,超多南亞中東人聽懂廣東話讚好。也出動宇宙漿緊身樽領,含含取樣棒,搖搖碌試管,幾撚落力,唔講以為可以測埋大肺活量基因。
有DNA就知肺活量都不錯,方便選妃。(Btw原來真係有日本人做大波貧乳的基因研究:https://www.nature.com/articles/s41598-018-25065-9)
同時也有10000部Youtube影片,追蹤數超過2,910的網紅コバにゃんチャンネル,也在其Youtube影片中提到,...
「whole exome sequencing」的推薦目錄:
- 關於whole exome sequencing 在 北歐心科學 NordicHearts Facebook 的最讚貼文
- 關於whole exome sequencing 在 Faithy Vanity Table Facebook 的精選貼文
- 關於whole exome sequencing 在 國家衛生研究院-論壇 Facebook 的最佳貼文
- 關於whole exome sequencing 在 コバにゃんチャンネル Youtube 的最佳解答
- 關於whole exome sequencing 在 大象中醫 Youtube 的最讚貼文
- 關於whole exome sequencing 在 大象中醫 Youtube 的精選貼文
whole exome sequencing 在 Faithy Vanity Table Facebook 的精選貼文
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whole exome sequencing 在 國家衛生研究院-論壇 Facebook 的最佳貼文
➥ 臨床發現年輕無慢性病史的男性染病後可能成為新冠肺炎重症病患,原發性免疫功能不全為可能造成其重症的原因之一,Hoischen博士和其研究團隊針對四位無慢性病史的新冠肺炎重症年輕男性病患進行全外顯子定序(whole-exome sequencing)。
結果發現這四位無慢性病史的新冠肺炎重症年輕男性病患均帶有toll-like receptor 7 (TLR7) 基因功能缺失(loss-of-function)的基因變異,研究結果指出個案感染新冠肺炎後可能因自身帶有TLR7基因變異,而導致TLR7基因的功能缺失,造成干擾素第一型和第二型免疫功能不全,有一定程度的關聯。
初步研究結果可作為感染新冠肺炎後病理機制之參考。( 財團法人國家衛生研究院 蔡慧如博士摘要整理,完整文章,詳:http://forum.nhri.org.tw/covid19/virus/j_translate/j1913/)
📋 JAMA - 2020-07-24
Presence of Genetic Variants Among Young Men With Severe COVID-19
■ Author:Caspar I. van der Made CI, Simons A, Schuurs-Hoeijmakers J, et al.
■ Linkhttps://jamanetwork.com/journals/jama/fullarticle/2768926
〈 國家衛生研究院-論壇 〉
➥ COVID-19學術資源-轉譯文章 - 2020/08/26
衛生福利部
疾病管制署 - 1922防疫達人
疾病管制署
whole exome sequencing 在 コバにゃんチャンネル Youtube 的最佳解答
whole exome sequencing 在 大象中醫 Youtube 的最讚貼文
whole exome sequencing 在 大象中醫 Youtube 的精選貼文
whole exome sequencing 在 What are whole exome sequencing and whole genome ... 的相關結果
Together, all the exons in a genome are known as the exome, and the method of sequencing them is known as whole exome sequencing. This method ... ... <看更多>
whole exome sequencing 在 Whole-Exome Sequencing - Yourgene Health 的相關結果
Whole -Exome Sequencing 技術,於臨床運用上不僅能夠作為快速定位單基因致病疾病的有力工具,也能應用研究多基因/點位變異的複雜疾病,如糖尿病、高血壓和腫瘤等。 ... <看更多>
whole exome sequencing 在 NGS 次世代定序服務Whole Exome Sequencing 的相關結果
Whole Exome Sequencing NGS Service. 人類Exon 區域僅占全基因體不到2%,卻有近85% 疾病發生在外顯子區域的變異,因此研究與SNPs 相關疾病常著重於Exome,更可大幅 ... ... <看更多>