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Illumina 平台全基因组亚硫酸氢盐测序的数据质量。

Data quality of whole genome bisulfite sequencing on Illumina platforms.

机构信息

Department of Medical Sciences, Molecular Medicine and Science for Life Laboratory, Uppsala University, Uppsala, Sweden.

出版信息

PLoS One. 2018 Apr 18;13(4):e0195972. doi: 10.1371/journal.pone.0195972. eCollection 2018.

Abstract

The powerful HiSeq X sequencers with their patterned flowcell technology and fast turnaround times are instrumental for many large-scale genomic and epigenomic studies. However, assessment of DNA methylation by sodium bisulfite treatment results in sequencing libraries of low diversity, which may impact data quality and yield. In this report we assess the quality of WGBS data generated on the HiSeq X system in comparison with data generated on the HiSeq 2500 system and the newly released NovaSeq system. We report a systematic issue with low basecall quality scores assigned to guanines in the second read of WGBS when using certain Real Time Analysis (RTA) software versions on the HiSeq X sequencer, reminiscent of an issue that was previously reported with certain HiSeq 2500 software versions. However, with the HD.3.4.0 /RTA 2.7.7 software upgrade for the HiSeq X system, we observed an overall improved quality and yield of the WGBS data generated, which in turn empowers cost-effective and high quality DNA methylation studies.

摘要

高通量 HiSeq X 测序仪及其独特的图案化流动池技术和快速周转时间,是许多大规模基因组学和表观基因组学研究的重要工具。然而,亚硫酸氢盐处理评估 DNA 甲基化会导致测序文库多样性降低,这可能会影响数据质量和产量。在本报告中,我们评估了在 HiSeq X 系统上生成的 WGBS 数据的质量,并将其与在 HiSeq 2500 系统和新发布的 NovaSeq 系统上生成的数据进行比较。我们报告了一个系统问题,即在使用特定的实时分析(RTA)软件版本在 HiSeq X 测序仪上进行 WGBS 时,第二个读取的鸟嘌呤碱基的碱基质量评分较低,这让人联想到之前在某些 HiSeq 2500 软件版本中报告的问题。然而,通过对 HiSeq X 系统的 HD.3.4.0 /RTA 2.7.7 软件升级,我们观察到 WGBS 数据的整体质量和产量得到了提高,这反过来又为具有成本效益的高质量 DNA 甲基化研究提供了支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68dd/5905984/6a508f17d943/pone.0195972.g001.jpg

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