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TNER: a novel background error suppression method for mutation detection in circulating tumor DNA

机译:TNER:一种用于循环肿瘤DNA突变检测的新型背景误差抑制方法

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Ultra-deep next-generation sequencing of circulating tumor DNA (ctDNA) holds great promise as a tool for the early detection of cancer and for monitoring disease progression and therapeutic responses. However, the low abundance of ctDNA in the bloodstream coupled with technical errors introduced during library construction and sequencing complicates mutation detection. To achieve high accuracy of variant calling via better distinguishing low-frequency ctDNA mutations from background errors, we introduce TNER (Tri-Nucleotide Error Reducer), a novel background error suppression method that provides a robust estimation of background noise to reduce sequencing errors. The results on both simulated data and real data from healthy subjects demonstrate that the proposed algorithm consistently outperforms a current, state-of-the-art, position-specific error polishing model, particularly when the sample size of healthy subjects is small. TNER significantly enhances the specificity of downstream ctDNA mutation detection without sacrificing sensitivity. The tool is publicly available at https://github.com/ctDNA/TNER .
机译:循环肿瘤DNA(ctDNA)的超深度下一代测序技术有望作为癌症早期检测,监测疾病进展和治疗反应的工具。但是,血液中ctDNA的低丰度以及在文库构建和测序过程中引入的技术错误使突变检测变得复杂。为了通过更好地将低频ctDNA突变与背景错误区分开来实现变异调用的高精度,我们引入了TNER(三核苷酸错误减少剂),这是一种新颖的背景错误抑制方法,可提供可靠的背景噪声估计以减少测序错误。来自健康受试者的模拟数据和真实数据的结果均表明,所提出的算法始终优于当前的最新技术,针对特定位置的误差修正模型,尤其是在健康受试者的样本量较小时。 TNER可显着增强下游ctDNA突变检测的特异性,而不会牺牲灵敏度。该工具可从https://github.com/ctDNA/TNER公开获得。

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