Q2 Solutions - EA Genomics, Morrisville, NC, USA.
Kelly Government Solutions, Rockville, MD, USA.
Sci Rep. 2019 May 6;9(1):6980. doi: 10.1038/s41598-019-43282-8.
The National Cancer Institute conducted the Biospecimen Pre-analytical Variables (BPV) study to determine the effects of formalin fixation and delay to fixation (DTF) on the analysis of nucleic acids. By performing whole transcriptome sequencing and small RNA profiling on matched snap-frozen and FFPE specimens exposed to different delays to fixation, this study aimed to determine acceptable delays to fixation and proper workflow for accurate and reliable Next-Generation Sequencing (NGS) analysis of FFPE specimens. In comparison to snap-freezing, formalin fixation changed the relative proportions of intronic/exonic/untranslated RNA captured by RNA-seq for most genes. The effects of DTF on NGS analysis were negligible. In 80% of specimens, a subset of RNAs was found to differ between snap-frozen and FFPE specimens in a consistent manner across tissue groups; this subset was unaffected in the remaining 20% of specimens. In contrast, miRNA expression was generally stable across various formalin fixation protocols, but displayed increased variability following a 12 h delay to fixation.
美国国立癌症研究所进行了生物标本前分析变量(BPV)研究,以确定福尔马林固定和固定延迟(DTF)对核酸分析的影响。通过对匹配的 snap 冷冻和 FFPE 标本进行全转录组测序和小 RNA 分析,这些标本暴露于不同的固定延迟,本研究旨在确定可接受的固定延迟和适当的工作流程,以实现 FFPE 标本的准确可靠的下一代测序(NGS)分析。与 snap 冷冻相比,福尔马林固定改变了大多数基因的 RNA 测序捕获的内含子/外显子/非翻译 RNA 的相对比例。DTF 对 NGS 分析的影响可以忽略不计。在 80%的标本中,一小部分 RNA 在 snap 冷冻和 FFPE 标本之间存在一致的差异,在剩余的 20%的标本中则没有差异。相比之下,miRNA 表达在各种福尔马林固定方案中通常是稳定的,但在固定延迟 12 小时后显示出更大的可变性。