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首页> 外文期刊>Molecular and Cellular Endocrinology >Identification of novel epididymal genes by expression profiling and in silico gene discovery.
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Identification of novel epididymal genes by expression profiling and in silico gene discovery.

机译:通过表达谱分析和计算机模拟基因发现鉴定新的附睾基因。

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We have used both the UniGene RIKEN epididymal EST library and the Affymetrix microarray profiling for identifying novel epididymal genes in mouse. The use of ESTs is a complementary approach to Affymetrix arrays for identifying novel epididymal genes, while only 32% and 28% of ESTs of unknown genes were present in the U74v.2Set and MG 430 2.0 version Affymetrix arrays, respectively. As expected, the probe set for a notably larger proportion of known genes was present in the Affymetrix arrays, and the coverage was greatly improved by the newer array version. Furthermore, many genes with more than five ESTs in the UniGene library showed variable levels of expression in both versions of the Affymetrix arrays. However, both the Affymetrix and EST data correlated well with that obtained by quantitative RT-PCR, and thus, we conclude that the findings of high EST number but only limited expression in the arrays could be considered as false negatives in the Affymetrix arrays.
机译:我们已使用UniGene RIKEN附睾EST文库和Affymetrix微阵列分析来鉴定小鼠中的新附睾基因。 EST的使用是Affymetrix阵列的补充方法,用于识别新的附睾基因,而U74v.2Set和MG 430 2.0版本的Affymetrix阵列中分别存在未知基因的EST分别只有32%和28%。不出所料,Affymetrix阵列中存在用于已知基因的比例明显更高的探针组,并且更新的阵列版本极大地提高了覆盖率。此外,UniGene库中许多具有五个以上EST的基因在两个版本的Affymetrix阵列中均显示出可变的表达水平。然而,Affymetrix和EST数据均与定量RT-PCR获得的数据相关性很好,因此,我们得出的结论是,EST数量高但阵列中表达有限的发现可被视为Affymetrix阵列中的假阴性。

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