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多重骨髓瘤中通过连锁阅读测序和全外显子组测序检测到的结构变异和短变异的比较

Comparison of Structural and Short Variants Detected by Linked-Read and Whole-Exome Sequencing in Multiple Myeloma.

作者信息

Kumar Ashwini, Adhikari Sadiksha, Kankainen Matti, Heckman Caroline A

机构信息

Institute for Molecular Medicine Finland-FIMM, HiLIFE-Helsinki Institute of Life Science, iCAN Digital Cancer Medicine Flagship, University of Helsinki, Tukholmankatu 8, 00290 Helsinki, Finland.

iCAN Digital Precision Cancer Medicine, University of Helsinki, 00014 Helsinki, Finland.

出版信息

Cancers (Basel). 2021 Mar 10;13(6):1212. doi: 10.3390/cancers13061212.

Abstract

Linked-read sequencing was developed to aid the detection of large structural variants (SVs) from short-read sequencing efforts. We performed a systematic evaluation to determine if linked-read exome sequencing provides more comprehensive and clinically relevant information than whole-exome sequencing (WES) when applied to the same set of multiple myeloma patient samples. We report that linked-read sequencing detected a higher number of SVs (n = 18,455) than WES (n = 4065). However, linked-read predictions were dominated by inversions (92.4%), leading to poor detection of other types of SVs. In contrast, WES detected 56.3% deletions, 32.6% insertions, 6.7% translocations, 3.3% duplications and 1.2% inversions. Surprisingly, the quantitative performance assessment suggested a higher performance for WES (AUC = 0.791) compared to linked-read sequencing (AUC = 0.766) for detecting clinically validated cytogenetic alterations. We also found that linked-read sequencing detected more short variants (n = 704) compared to WES (n = 109). WES detected somatic mutations in all MM-related genes while linked-read sequencing failed to detect certain mutations. The comparison of somatic mutations detected using linked-read, WES and RNA-seq revealed that WES and RNA-seq detected more mutations than linked-read sequencing. These data indicate that WES outperforms and is more efficient than linked-read sequencing for detecting clinically relevant SVs and MM-specific short variants.

摘要

联读测序技术的开发旨在辅助从短读长测序结果中检测大的结构变异(SVs)。我们进行了一项系统评估,以确定当应用于同一组多发性骨髓瘤患者样本时,联读外显子测序是否比全外显子测序(WES)提供更全面且与临床相关的信息。我们报告称,联读测序检测到的SVs数量(n = 18,455)高于WES(n = 4065)。然而,联读预测主要为倒位(92.4%),导致对其他类型SVs的检测效果不佳。相比之下,WES检测到56.3%的缺失、32.6%的插入、6.7%的易位、3.3%的重复和1.2%的倒位。令人惊讶的是,定量性能评估表明,在检测经临床验证的细胞遗传学改变方面,WES(AUC = 0.791)的性能高于联读测序(AUC = 0.766)。我们还发现,与WES(n = 109)相比,联读测序检测到更多的短变异(n = 704)。WES在所有MM相关基因中检测到体细胞突变,而联读测序未能检测到某些突变。对联读、WES和RNA测序检测到的体细胞突变进行比较发现,WES和RNA测序检测到的突变比联读测序更多。这些数据表明,在检测与临床相关的SVs和MM特异性短变异方面,WES优于联读测序且更高效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2299/7999337/855be13bf086/cancers-13-01212-g001.jpg

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