首页> 外文期刊>Bioinformatics >NORMAL: accurate nucleosome positioning using a modified Gaussian mixture model
【24h】

NORMAL: accurate nucleosome positioning using a modified Gaussian mixture model

机译:正常:使用改良的高斯混合模型进行精确的核小体定位

获取原文
获取原文并翻译 | 示例
       

摘要

Motivation: Nucleosomes are the basic elements of chromatin structure. They control the packaging of DNA and play a critical role in gene regulation by allowing physical access to transcription factors. The advent of second-generation sequencing has enabled landmark genome-wide studies of nucleosome positions for several model organisms. Current methods to determine nucleosome positioning first compute an occupancy coverage profile by mapping nucleosome-enriched sequenced reads to a reference genome; then, nucleosomes are placed according to the peaks of the coverage profile. These methods are quite accurate on placing isolated nucleosomes, but they do not properly handle more complex configurations. Also, they can only provide the positions of nucleosomes and their occupancy level, whereas it is very beneficial to supply molecular biologists additional information about nucleosomes like the probability of placement, the size of DNA fragments enriched for nucleosomes and/or whether nucleosomes are well positioned or 'fuzzy' in the sequenced cell sample. Results: We address these issues by providing a novel method based on a parametric probabilistic model. An expectation maximization algorithm is used to infer the parameters of the mixture of distributions. We compare the performance of our method on two real datasets against Template Filtering, which is considered the current state-of-the-art. On synthetic data, we show that our method can resolve more accurately complex configurations of nucleosomes, and it is more robust to user-defined parameters. On real data, we show that our method detects a significantly higher number of nucleosomes.
机译:动机:核小体是染色质结构的基本元素。它们控制DNA的包装,并通过允许物理访问转录因子在基因调控中发挥关键作用。第二代测序技术的出现,使得对几种模型生物的核小体位置进行了具有里程碑意义的全基因组研究。当前确定核小体定位的方法首先通过将富集了核小体的测序读段映射到参考基因组来计算占用覆盖率谱;然后,根据覆盖图谱的峰放置核小体。这些方法在放置分离的核小体时非常准确,但是它们不能正确处理更复杂的构型。而且,它们只能提供核小体的位置及其占用水平,而向分子生物学家提供有关核小体的其他信息(如放置的可能性,富集了核小体的DNA片段的大小和/或核小体是否位置正确)非常有益。或“模糊”在已排序的细胞样本中。结果:我们通过提供一种基于参数概率模型的新颖方法来解决这些问题。期望最大化算法用于推断分布混合的参数。我们将我们的方法在两个真实数据集上与模板过滤(目前被认为是最新技术)的性能进行了比较。在合成数据上,我们表明我们的方法可以更准确地解析核小体的复杂构型,并且对用户定义的参数更可靠。在真实数据上,我们表明我们的方法可检测到明显更高数量的核小体。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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