首页> 外文期刊>Frontiers in bioscience: a journal and virtual library >STATISTICAL METHODS FOR DETECTING GENOMIC ALTERATIONS THROUGH ARRAY-BASED COMPARATIVE GENOMIC HYBRIDIZATION (CGH)
【24h】

STATISTICAL METHODS FOR DETECTING GENOMIC ALTERATIONS THROUGH ARRAY-BASED COMPARATIVE GENOMIC HYBRIDIZATION (CGH)

机译:通过基于阵列的比较基因组杂交(CGH)检测基因组变化的统计方法

获取原文
获取原文并翻译 | 示例
           

摘要

Array-based comparative genomic hybridization (ABCGH) is an emerging high-resolution and high-throughput molecular genetic technique that allows genome-wide screening for chromosome alterations associated with tumorigenesis Like the cDNA microarrays, ABCGH uses two differentially labeled test and reference DNAs which are cohybridized to cloned genomic fragments immobilized on glass slides The hybridized DNAs are then detected in two different fiuorochromes, and the significant deviation from unity in the ratios of the digitized intensity values is indicative of copy-number differences between the test and reference genomes. Proper statistical analyses need to account for many sources of variation besides genuine differences between the two genomes. In particular, spatial correlations, the variable nature of the ratio variance and non-Normal distribution call for careful statistical modeling. We propose two new statistics, the standard t-statistic and its modification with variances smoothed along the genome, and two tests for each statistic, the standard t-test and a test based on the hybrid adaptive spline (HAS) Simulations indicate that the smoothed t-statistic always improves the performance over the standard t-statistic. The t-tests are more powerful in -detecting isolated alterations while those based on HAS are more powerful in detecting a cluster of alterations We apply the proposed methods to the identification of genomic alterations in endometrium in women with endometriosis.
机译:基于阵列的比较基因组杂交(ABCGH)是一种新兴的高分辨率和高通量分子遗传技术,可用于在全基因组范围内筛选与肿瘤发生相关的染色体改变。与cDNA微阵列一样,ABCGH使用两个差异标记的测试DNA和参考DNA。共杂交到固定在载玻片上的克隆基因组片段。然后在两种不同的荧光染料中检测到杂交的DNA,数字化强度值之比与单位的显着偏离表明了测试基因组与参考基因组之间的拷贝数差异。正确的统计分析除了两个基因组之间的真正差异外,还需要考虑许多变异来源。特别是,空间相关性,比率方差的变量性质和非正态分布要求进行仔细的统计建模。我们提出了两个新的统计量,即标准t统计量及其沿基因组平滑的方差的修正,以及针对每个统计量的两个检验,标准t检验和基于混合自适应样条(HAS)的检验,模拟表明t统计量总是比标准t统计量提高性能。 t检验在检测孤立变异方面更有效,而基于HAS的t检验在检测一组变异方面更有效。我们将提出的方法应用于子宫内膜异位症妇女子宫内膜的基因组变异鉴定。

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