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RNA 测序中反转录反应的假象和偏差。

Artifacts and biases of the reverse transcription reaction in RNA sequencing.

机构信息

OncoRNALab, Cancer Research Institute Ghent, 9000 Ghent, Belgium

Department of Biomolecular Medicine, Ghent University, 9000 Ghent, Belgium.

出版信息

RNA. 2023 Jul;29(7):889-897. doi: 10.1261/rna.079623.123. Epub 2023 Mar 29.

Abstract

RNA sequencing has spurred a significant number of research areas in recent years. Most protocols rely on synthesizing a more stable complementary DNA (cDNA) copy of the RNA molecule during the reverse transcription reaction. The resulting cDNA pool is often wrongfully assumed to be quantitatively and molecularly similar to the original RNA input. Sadly, biases and artifacts confound the resulting cDNA mixture. These issues are often overlooked or ignored in the literature by those that rely on the reverse transcription process. In this review, we confront the reader with intra- and intersample biases and artifacts caused by the reverse transcription reaction during RNA sequencing experiments. To fight the reader's despair, we also provide solutions to most issues and inform on good RNA sequencing practices. We hope the reader can use this review to their advantage, thereby contributing to scientifically sound RNA studies.

摘要

RNA 测序近年来激发了大量的研究领域。大多数方案都依赖于在逆转录反应中合成 RNA 分子更稳定的互补 DNA(cDNA)拷贝。由此产生的 cDNA 池通常被错误地认为在定量和分子上与原始 RNA 输入相似。遗憾的是,偏倚和假象使 cDNA 混合物变得复杂。在文献中,那些依赖逆转录过程的人往往会忽略或忽视这些问题。在这篇综述中,我们向读者介绍了 RNA 测序实验中逆转录反应引起的样本内和样本间的偏倚和假象。为了消除读者的绝望,我们还为大多数问题提供了解决方案,并介绍了良好的 RNA 测序实践。我们希望读者能够利用这篇综述为自己带来优势,从而为科学合理的 RNA 研究做出贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee49/10275267/3acacac23b57/889f01.jpg

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