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Next-generation sequencing and microarray-based interrogation of microRNAs from formalin-fixed paraffin-embedded tissue: Preliminary assessment of cross-platform concordance

机译:福尔马林固定的石蜡包埋组织中的microRNA的下一代测序和基于微阵列的询问:跨平台一致性的初步评估

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摘要

Next-generation sequencing is increasingly employed in biomedical investigations. Strong concordance between microarray and mRNA-seq levels has been reported in high quality specimens but information is lacking on formalin-fixed, paraffin-embedded (FFPE) tissues, and particularly for microRNA (miRNA) analysis. We conducted a preliminary examination of the concordance between miRNA-seq and cDNA-mediated annealing, selection, extension, and ligation (DASL) miRNA assays. Quantitative agreement between platforms is moderate (Spearman correlation 0.514–0.596) and there is discordance of detection calls on a subset of miRNAs. Quantitative PCR (q-RT-PCR) performed for several discordant miRNAs confirmed the presence of most sequences detected by miRNA-seq but not by DASL but also that miRNA-seq did not detect some sequences, which DASL confidently detected. Our results suggest that miRNA-seq is specific, with few false positive calls, but it may not detect certain abundant miRNAs in FFPE tissue. Further work is necessary to fully address these issues that are pertinent for translational research.
机译:下一代测序越来越多地用于生物医学研究中。高质量标本中已经报道了微阵列和mRNA-seq水平之间的高度一致性,但是在福尔马林固定,石蜡包埋(FFPE)的组织上,尤其是在microRNA(miRNA)分析方面,缺乏信息。我们对miRNA-seq和cDNA介导的退火,选择,延伸和连接(DASL)miRNA分析之间的一致性进行了初步检查。平台之间的定量一致性适中(Spearman相关系数0.514–0.596),并且在miRNA的一个子集上检测调用存在不一致。对几种不一致的miRNA进行的定量PCR(q-RT-PCR)证实了miRNA-seq而非DASL所检测到的大多数序列的存在,而且miRNA-seq并未检测到DASL自信地检测到的某些序列。我们的结果表明,miRNA-seq具有特异性,几乎没有假阳性,但它可能无法在FFPE组织中检测到某些丰富的miRNA。为了进一步解决与翻译研究有关的这些问题,有必要做进一步的工作。

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