首页> 美国卫生研究院文献>other >The Quality Sequencing Minimum (QSM): providing comprehensive consistent transparent next generation sequencing  data quality assurance
【2h】

The Quality Sequencing Minimum (QSM): providing comprehensive consistent transparent next generation sequencing  data quality assurance

机译:最低质量测序(QSM):提供全面一致透明的下一代测序数据质量保证

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Next generation sequencing (NGS) is routinely used in clinical genetic testing. Quality management of NGS testing is essential to ensure performance is consistently and rigorously evaluated. Three primary metrics are used in NGS quality evaluation: depth of coverage, base quality and mapping quality. To provide consistency and transparency in the utilisation of these metrics we present the Quality Sequencing Minimum (QSM). The QSM defines the minimum quality requirement a laboratory has selected for depth of coverage (C), base quality (B) and mapping quality (M) and can be applied per base, exon, gene or other genomic region, as appropriate. The QSM format is CX_BY(P Y)_MZ(P Z). X is the parameter threshold for C, Y the parameter threshold for B, P Y the percentage of reads that must reach Y, Z the parameter threshold for M, P Z the percentage of reads that must reach Z. The data underlying the QSM is in the BAM file, so a QSM can be easily and automatically calculated in any NGS pipeline. We used the QSM to optimise cancer predisposition gene testing using the TruSight Cancer Panel (TSCP). We set the QSM as C50_B10(85)_M20(95). Test regions falling below the QSM were automatically flagged for review, with 100/1471 test regions QSM-flagged in multiple individuals. Supplementing these regions with 132 additional probes improved performance in 85/100. We also used the QSM to optimise testing of genes with pseudogenes such as PTEN and PMS2. In TSCP data from 960 individuals the median number of regions that passed QSM per sample was 1429 (97%).  Importantly, the QSM can be used at an individual report level to provide succinct, comprehensive quality assurance information about individual test performance. We believe many laboratories would find the QSM useful. Furthermore, widespread adoption of the QSM would facilitate consistent, transparent reporting of genetic test performance by different laboratories.
机译:下一代测序(NGS)通常用于临床基因测试。 NGS测试的质量管理对于确保对性能进行一致且严格的评估至关重要。 NGS质量评估中使用了三个主要指标:覆盖深度,基本质量和地图质量。为了在使用这些指标时提供一致性和透明性,我们提出了最低质量测序(QSM)。 QSM定义了实验室为覆盖深度(C),碱基质量(B)和作图质量(M)选择的最低质量要求,并且可以根据需要在每个碱基,外显子,基因或其他基因组区域应用。 QSM格式为CX_BY(P Y)_MZ(P Z)。 X是C的参数阈值,Y是B的参数阈值,PY是必须达到Y的读取百分比,Z是M的参数阈值,PZ必须达到Z的读取百分比。QSM的数据位于BAM文件,因此可以在任何NGS管道中轻松自动地计算QSM。我们使用QSM使用TruSight Cancer Panel(TSCP)优化了癌症易感基因测试。我们将QSM设置为C50_B10(85)_M20(95)。低于QSM的测试区域会被自动标记以供审查,其中多个个体中有100/1471个QSM标记了测试区域。用132个附加探针补充这些区域,从而提高了85/100的性能。我们还使用QSM优化了带有PTEN和PMS2等假基因的基因测试。在来自960个个体的TSCP数据中,每个样本通过QSM的区域的中位数为1429(97%)。重要的是,可以在单个报告级别使用QSM,以提供有关单个测试性能的简洁,全面的质量保证信息。我们相信许多实验室会发现QSM有用。此外,QSM的广泛采用将促进不同实验室对基因测试性能的一致,透明的报告。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号