Department of Medical Genetics, Oslo University Hospital and University of Oslo , Oslo, Norway.
Department of Biostatistics, Oslo Centre for Biostatistics and Epidemiology, University of Oslo , Oslo, Norway.
RNA Biol. 2020 Sep;17(9):1284-1292. doi: 10.1080/15476286.2020.1761081. Epub 2020 May 21.
High-throughput sequencing has emerged as the favoured method to study microRNA (miRNA) expression, but biases introduced during library preparation have been reported. We recently compared the performance (sensitivity, reliability, titration response and differential expression) of six commercially-available kits on synthetic miRNAs and human RNA, where library preparation was performed by the vendors. We hereby supplement this study with data from two further commonly used kits (NEBNext, NEXTflex) whose manufacturers initially declined to participate. NEXTflex demonstrated the highest sensitivity, which may reflect its use of partially-randomized adapter sequences, but overall performance was lower than the QIAseq and TailorMix kits. NEBNext showed intermediate performance. We reaffirm that biases are kit specific, complicating the comparison of miRNA datasets generated using different kits.
高通量测序已成为研究 microRNA(miRNA)表达的首选方法,但已有报道称文库制备过程中存在偏倚。我们最近比较了六种市售试剂盒在合成 miRNA 和人 RNA 上的性能(灵敏度、可靠性、滴定反应和差异表达),其中文库制备由供应商完成。在此基础上,我们补充了来自另外两种常用试剂盒(NEBNext,NEXTflex)的数据,其制造商最初拒绝参与。NEXTflex 表现出最高的灵敏度,这可能反映了其使用部分随机接头序列,但总体性能低于 QIAseq 和 TailorMix 试剂盒。NEBNext 表现出中等性能。我们再次确认偏倚是试剂盒特异性的,这使得使用不同试剂盒生成的 miRNA 数据集的比较变得复杂。