Impact of RNA degradation on next-generation sequencing transcriptome data

被引:18
作者
Lu, Wenxiang [1 ]
Zhou, Qin [2 ]
Chen, Yi [2 ]
机构
[1] Southeast Univ, Sch Biol Sci & Med Engn, State Key Lab Bioelect, Nanjing 210096, Jiangsu, Peoples R China
[2] Kunshan Hosp Tradit Chinese Med, Dept Obstet & Gynecol, Kunshan 215300, Peoples R China
关键词
RNA-seq; RNA degradation; RNA integrity number; Enrichment pathways; QUALITY-CONTROL; SEQ; ANNOTATION;
D O I
10.1016/j.ygeno.2022.110429
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
RNA sequencing is an innovative technology to study transcriptomes in both biological and clinical research. However, clinical specimens from patients undergoing surgical operations have a major challenge due to sample degradation. This study replicated the process of RNA degradation by maintaining cells at room temperature to achieve none, slight, middle, and high levels of RNA degradation with decreasing RNA integrity numbers (RIN) of approximately 9.8, 6.7, 4.4, and 2.5, respectively. Next, the differential expression of mRNA and long noncoding RNA (lncRNA) was analyzed in the four degradation groups along with pathway enrichment analysis. The results showed that the similarity of lncRNAs exhibited significant differences even for a slight level of RNA degradation compared with the non-degraded RNA sample. Also, the RNA degradation process was found to be universal, global, and random; the differentially expressed genes increased with an increase in degradation but the pathway enrichment phenomenon was not significantly observed.
引用
收藏
页数:8
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