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Comparative analysis of novel MGISEQ-2000 sequencing platform vs Illumina HiSeq 2500 for whole-genome sequencing

机译:新型MGISEQ-2000测序平台对比较分析VS Illumina Hiseq 2500进行全基因组测序

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摘要

The MGISEQ-2000 developed by MGI Tech Co. Ltd. (a subsidiary of the BGI Group) is a new competitor of such next-generation sequencing platforms as NovaSeq and HiSeq (Illumina). Its sequencing principle is based on the DNB and the cPAS technologies, which were also used in the previous version of the BGISEQ-500 device. However, the reagents for MGISEQ-2000 have been refined and the platform utilizes updated software. The cPAS method is an advanced technology based on the cPAL previously created by Complete Genomics. In this paper, the authors compare the results of the whole-genome sequencing of a DNA sample from a Russian female donor performed on MGISEQ-2000 and Illumina HiSeq 2500 (both PE150). Two platforms were compared in terms of sequencing quality, number of errors and performance. Additionally, we performed variant calling using four different software packages: Samtools mpileaup, Strelka2, Sentieon, and GATK. The accuracy of SNP detection was similar in the data generated by MGISEQ-2000 and HiSeq 2500, which was used as a reference. At the same time, a separate indel analysis of the overall error rate revealed similar FPR values and lower sensitivity. It may be concluded with confidence that the data generated by the analyzed sequencing systems is characterized by comparable magnitudes of error and that MGISEQ-2000 and HiSeq 2500 can be used interchangeably for similar tasks like whole genome sequencing.
机译:MGI Tech Co. Ltd.(BGI集团的子公司)开发的MGiseq-2000是该等新一代测序平台的新竞争对手,作为Novaseq和Hiseq(Illumina)。其排序原理基于DNB和CPAS技术,该技术也用于BGISEQ-500设备的先前版本。然而,MGiseQ-2000的试剂已被精制,平台利用更新的软件。 CPAS方法是基于先前由完整基因组学创建的CPAL的高级技术。在本文中,作者将DNA样品的全基因组测序从对Mgiseq-2000和Illumina Hiseq 2500(PE150)进行的俄罗斯雌性供体的全基因组测序结果进行比较。在测序质量,错误和性能数量方面进行比较两个平台。此外,我们使用四个不同的软件包进行了变体调用:Samtools Mpileaup,Strelka2,Sentieon和Gatk。 SNP检测的准确性在MGISEQ-2000和HISEQ 2500产生的数据中类似地用作参考。同时,对整体错误率的单独indel分析显示出类似的FPR值和较低的灵敏度。可以置信地结束,即分析的测序系统产生的数据的特征在于相当的误差幅度,并且MGiseQ-2000和Hiseq 2500可以互换使用,以适用于全基因组测序的类似任务。

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