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A SIGNAL PROCESSINNG ATTEMPT TO IDENTIFY CELL DIVISION CYCLE (CDC) m-RNAs REVEALS COUPLINGS WITH OTHER CELL CYCLES

机译:鉴定细胞分裂周期(CDC)m-RNA揭示与其他细胞周期的偶联的信号过程

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Periodic expression patterns from microarray experiments with peaks in some mitotic stages have been considered for different species. It has been important to unravel transcriptional program advancing the cell cycle progression in aim that encompasses either combating disease or cognition of different cellular phenomena.rnDespite the high throughput in evaluating transcripts, microarray is not effective for lowly expressed genes and is sensitive to experimental conditions, de-synchronization of transcripts, cross-hybridization or other technical issues.rnTo overcome these limitations a new signal processing method of a compensatory role has been devised to address CDC-regulated genes. By this method, the comparison results of the CDC m-RNAs from two different expression sets of microarray experiments are provided.rnWhile genes from previous such studies were poorly overlapped, herein an accord of -80% has been gained. The obtained results conform to the coarse clustering approach.rnWhile trying to settle the specificity issue in the presence of a great number of periodic genes being detected the hypothesis on other categories of genes being in regular co-expression with the CDC regulated genes in experimental conditions could be confirmed. Namely, some metabolic and the Met-biosynthesis pathway m-RNAs have been found phase entrained with CDC thus indicating possible couplings.
机译:对于不同物种,已经考虑了来自微阵列实验的周期表达模式,该实验在某些有丝分裂阶段出现了峰值。揭露促进细胞周期进程的转录程序非常重要,其目的既包括与疾病作斗争,也包括对不同细胞现象的认识。rn尽管评估转录本的通量很高,微阵列对表达量低的基因无效,并且对实验条件敏感,为了克服这些局限性,为了克服这些限制,人们设计了一种具有补偿作用的新信号处理方法来解决CDC调控的基因。通过该方法,提供了来自两个不同表达组的微阵列实验的CDC m-RNA的比较结果。虽然来自先前此类研究的基因很少重叠,但是本文获得了-80%的一致性。获得的结果符合粗糙聚类方法。在尝试检测大量周期性基因的情况下尝试解决特异性问题时,关于其他类别基因与CDC调控基因在实验条件下定期共表达的假设可以确认。即,已经发现某些代谢和Met-生物合成途径的m-RNA被CDC相夹带,因此表明可能的偶联。

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