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QuaDMutEx: quadratic driver mutation explorer

机译:Quadmutex:二次驱动程序变异资源管理器

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摘要

Abstract Background Somatic mutations accumulate in human cells throughout life. Some may have no adverse consequences, but some of them may lead to cancer. A cancer genome is typically unstable, and thus more mutations can accumulate in the DNA of cancer cells. An ongoing problem is to figure out which mutations are drivers - play a role in oncogenesis, and which are passengers - do not play a role. One way of addressing this question is through inspection of somatic mutations in DNA of cancer samples from a cohort of patients and detection of patterns that differentiate driver from passenger mutations. Results We propose QuaDMutEx, a method that incorporates three novel elements: a new gene set penalty that includes non-linear penalization of multiple mutations in putative sets of driver genes, an ability to adjust the method to handle slow- and fast-evolving tumors, and a computationally efficient method for finding gene sets that minimize the penalty, through a combination of heuristic Monte Carlo optimization and exact binary quadratic programming. Compared to existing methods, the proposed algorithm finds sets of putative driver genes that show higher coverage and lower excess coverage in eight sets of cancer samples coming from brain, ovarian, lung, and breast tumors. Conclusions Superior ability to improve on both coverage and excess coverage on different types of cancer shows that QuaDMutEx is a tool that should be part of a state-of-the-art toolbox in the driver gene discovery pipeline. It can detect genes harboring rare driver mutations that may be missed by existing methods. QuaDMutEx is available for download from https://github.com/bokhariy/QuaDMutEx under the GNU GPLv3 license.
机译:摘要背景体细胞突变积累在整个生命的人类细胞。有些人可能没有不良后果,但他们中的一些可能会导致癌症的发生。甲癌症基因组通常是不稳定的,并且因此多个突变可在癌细胞的DNA积累。一直存在的问题是要弄清楚哪些突变是司机 - 在肿瘤中发挥作用,并有乘客 - 不发挥作用。解决这一问题的一种方式是通过在癌症样品的DNA的体细胞突变的检查从一组患者和检测图案,从乘客突变分化驱动程序。结果我们建议QuaDMutEx,并入三种新型元件的方法:一种新的基因组惩罚包括在推定的组驱动的基因的多个突变的非线性惩罚,以调节处理缓慢和快速发展的肿瘤的方法的能力,以及用于通过启发式蒙特卡洛优化和确切的二进制二次规划的组合发现的基因集,最大限度地减少了损失,在计算上高效的方法。相比于现有的方法,所提出的算法找到套显示较高的覆盖和更低的超额保险在八组脑,卵巢癌,肺癌和乳腺癌肿瘤癌症来的样品假定驱动基因。结论优于提高覆盖范围和不同类型的癌症显示多余的覆盖面,QuaDMutEx是一种工具,应该是国家的最先进的工具箱中的驱动性基因的发现管道的一部分能力。它可以检测基因窝藏可以通过现有的方法错过难得的驱动突变。 QuaDMutEx可以在GNU GPLv3的许可证从https://github.com/bokhariy/QuaDMutEx下载。

著录项

  • 作者

    Yahya Bokhari; Tomasz Arodz;

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  • 年度 2017
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  • 原文格式 PDF
  • 正文语种 eng
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