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Globin mRNA reduction for whole-blood transcriptome sequencing

机译:球蛋白mRNA降低可用于全血转录组测序

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The transcriptome analysis of whole-blood RNA by sequencing holds promise for the identification and tracking of biomarkers; however, the high globin mRNA (gmRNA) content of erythrocytes hampers whole-blood and buffy coat analyses. We introduce a novel gmRNA locking assay (GlobinLock, GL) as a robust and simple gmRNA reduction tool to preserve RNA quality, save time and cost. GL consists of a pair of gmRNA-specific oligonucleotides in RNA initial denaturation buffer that is effective immediately after RNA denaturation and adds only ten minutes of incubation to the whole cDNA synthesis procedure when compared to non-blood RNA analysis. We show that GL is fully effective not only for human samples but also for mouse and rat, and so far incompletely studied cow, dog and zebrafish.
机译:通过测序对全血RNA进行转录组分析,有望为生物标志物的鉴定和追踪提供依据。然而,高含量的珠蛋白mRNA(gmRNA)阻碍了全血和血沉棕黄层的分析。我们介绍了一种新颖的gmRNA锁定测定法(GlobinLock,GL),它是一种功能强大且简单的gmRNA还原工具,可保留RNA质量,节省时间和成本。 GL由在RNA初始变性缓冲液中的一对gmRNA特异性寡核苷酸组成,该片段在RNA变性后立即有效,并且与非血液RNA分析相比,在整个cDNA合成过程中仅增加了十分钟的孵育时间。我们表明,GL不仅对人体样品而且对小鼠和大鼠都是完全有效的,而且迄今为止对牛,狗和斑马鱼的研究还不完善。

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