首页> 外文期刊>Nucleic Acids Research >Absolute mRNA concentrations from sequence-specific calibration of oligonucleotide arrays
【24h】

Absolute mRNA concentrations from sequence-specific calibration of oligonucleotide arrays

机译:来自寡核苷酸阵列的序列特异性校准的绝对mRNA浓度

获取原文
获取原文并翻译 | 示例
           

摘要

Oligonucleotide microarrays are based on the hybridization of labeled mRNA molecules to short length oligonucleotide probes on a glass surface. Two effects have been shown to affect the raw data: the sequence dependence of the probe hybridization properties and the chemical saturation resulting from surface adsorption processes. We address both issues simultaneously using a physically motivated hybridization model. Based on publicly available calibration data sets, we show that Langmuir adsorption accurately describes GeneChip hybridization, with model parameters that we predict from the sequence composition of the probes. Because these parameters have physical units, we are able to estimate absolute mRNA concentrations in picomolar. Additionally, by accounting for chemical saturation, we substantially reduce the compressive bias of differential expression estimates that normally occurs toward high concentrations.
机译:寡核苷酸微阵列基于标记的mRNA分子与玻璃表面上短长度寡核苷酸探针的杂交。已显示出两种影响原始数据的效应:探针杂交特性的序列依赖性和表面吸附过程产生的化学饱和度。我们使用物理杂交模型同时解决这两个问题。基于可公开获得的校准数据集,我们表明Langmuir吸附能够准确描述GeneChip杂交,并具有根据探针序列组成预测的模型参数。由于这些参数具有物理单位,因此我们能够估算皮摩尔中的绝对mRNA浓度。此外,考虑到化学饱和度,我们大大降低了通常向高浓度发生的差异表达估计的压缩偏差。

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