双鱼座:一个准确和多功能的单一样本体细胞和生殖系变异来电者

Tamsen Dunn, G. Berry, Dorothea Emig-Agius, Yu Jiang, A. Iyer, N. Udar, Michael P. Strömberg
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引用次数: 2

摘要

一种可靠、准确地检测肿瘤样本中罕见DNA突变的方法对癌症研究至关重要。由于许多临床组织库只有ffpe降解的肿瘤样本,而没有来自健康组织的匹配正常样本,因此在没有匹配正常样本的情况下,能够从背景噪声中区分低频突变对研究特别重要。目前的变体调用器,如GATK和VarScan,专注于种系变体调用(用于检测孟德尔遗传模式下的遗传突变),或者,在FreeBayes和MuTect的情况下,专注于肿瘤-正常关节变体调用(使用正常样本帮助从背景噪声中区分低频体细胞突变)。我们介绍了双鱼座,一个由Illumina独家开发的肿瘤变体调用者,用于从下一代测序数据中检测低频突变。自2012年以来,双鱼座一直是Illumina Truseq Amplicon工作流程中不可或缺的一部分,可在BaseSpace和MiSeq测序平台上使用。自2015年以来,双鱼座已经在github上向公众开放。(https://github.com/Illumina/Pisces)从那时起,双鱼座变体调用团队继续开发双鱼座,并提供了一套变体调用工具,包括ReadStitcher, variant Phaser和variant Quality Recalibration工具,与核心变体调用者双鱼座一起使用。在这里,我们描述了双鱼座变体调用工具和核心算法。我们描述了双鱼座的常见用例(不一定限于体细胞变体调用)。我们还评估了双鱼座在体细胞和种系数据集上的表现,这些数据集来自鉴定良好的样本的滴定,以及来自500个ffpe治疗的临床试验肿瘤样本的样本,与其他变异的调用者相比。我们的研究结果表明,双鱼座在各种情况下都能给出非常准确的结果。我们推荐双鱼座的扩增子体细胞和种系变异召唤。
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Pisces: An Accurate and Versatile Single Sample Somatic and Germline Variant Caller
A method for robustly and accurately detecting rare DNA mutations in tumor samples is critical to cancer research. Because many clinical tissue repositories have only FFPE-degraded tumor samples, and no matched normal sample from healthy tissue available, being able to discriminate low frequency mutations from background noise in the absence of a matched normal sample is of particular importance to research. Current state of the art variant callers such as GATK and VarScan focus on germline variant calling (used for detecting inherited mutations following a Mendelian inheritance pattern) or, in the case of FreeBayes and MuTect, focus on tumor-normal joint variant calling (using the normal sample to help discriminate low frequency somatic mutations from back ground noise). We present Pisces, a tumor-only variant caller exclusively developed at Illumina for detecting low frequency mutations from next generation sequencing data. Pisces has been an integral part of the Illumina Truseq Amplicon workflow since 2012, and is available on BaseSpace and on the MiSeq sequencing platforms. Pisces has been available to the public on github, since 2015. (https://github.com/Illumina/Pisces) Since that time, the Pisces variant calling team have continued to develop Pisces, and have made available a suite of variant calling tools, including a ReadStitcher, Variant Phaser, and Variant Quality Recalibration tool, to be used along with the core variant caller, Pisces. Here, we describe the Pisces variant calling tools and core algorithms. We describe the common use cases for Pisces (not necessarily restricted to somatic variant calling). We also evaluate Pisces performance on somatic and germline datasets, both from the titration of well characterized samples, and from a corpus of 500 FFPE-treated clinical trial tumor samples, against other variant callers. Our results show that Pisces gives highly accurate results in a variety of contexts. We recommend Pisces for amplicon somatic and germline variant calling.
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