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An Alignment-Free Regression Approach for Estimating Allele-Specific Expression Using RNA-Seq Data

机译:使用RNA-Seq数据估计等位基因特异性表达的无比对回归方法

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RNA-seq technology enables large-scale studies of allele-specific expression (ASE), or the expression difference between maternal and paternal alleles. Here, we study ASE in animals for which parental RNA-seq data are available. While most methods for determining ASE rely on read alignment, read alignment either leads to reference bias or requires knowledge of genomic variants in each parental strain. When RNA-seq data are available for both parental strains of a hybrid animal, it is possible to infer ASE with minimal reference bias and without knowledge of parental genomic variants. Our approach first uses parental RNA-seq reads to discover maternal and paternal versions of transcript sequences. Using these alternative transcript sequences as features, we estimate abundance levels of transcripts in the hybrid animal using a modified lasso linear regression model. We tested our methods on synthetic data from the mouse transcriptome and compared our results with those of Trinity, a state-of-the-art de novo RNA-seq assembler. Our methods achieved high sensitivity and specificity in both identifying expressed transcripts and transcripts exhibiting ASE. We also ran our methods on real RNA-seq mouse data from two F1 samples with wild-derived parental strains and were able to validate known genes exhibiting ASE, as well as confirm the expected maternal contribution ratios in all genes and genes on the X chromosome.
机译:RNA-seq技术可用于大规模研究等位基因特异性表达(ASE)或母本和父本等位基因之间的表达差异。在这里,我们在有父母RNA-seq数据的动物中研究ASE。虽然大多数确定ASE的方法都依赖于阅读比对,但阅读比对要么导致参考偏差,要么需要了解每个亲本菌株中的基因组变异体。当RNA-seq数据可用于杂种动物的两个亲本品系时,有可能以最小的参考偏差推断ASE,而无需了解亲本基因组变体。我们的方法首先使用亲本RNA-seq读数来发现转录本序列的母本和父本版本。使用这些替代的转录物序列作为特征,我们使用改良的套索线性回归模型估算杂种动物中转录物的丰度水平。我们对来自小鼠转录组的合成数据测试了我们的方法,并将我们的结果与最新的从头RNA序列组装器Trinity的结果进行了比较。我们的方法在鉴定表达的转录本和表现出ASE的转录本中均获得了高灵敏度和特异性。我们还对来自具有野生来源的亲本菌株的两个F1样品的真实RNA-seq小鼠数据进行了研究,能够验证展示ASE的已知基因,并确认所有基因和X染色体上的基因的预期母体贡献率。

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