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ChIPmix: mixture model of regressions for two-color ChIP-chip analysis.

机译:ChIPmix:两色ChIP芯片分析的回归混合模型。

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MOTIVATION: Chromatin immunoprecipitation (ChIP) combined with DNA microarray is a high-throughput technology to investigate DNA-protein binding or chromatin/histone modifications. ChIP-chip data require adapted statistical method in order to identify enriched regions. All methods already proposed are based on the analysis of the log ratio (Ip/Input). Nevertheless, the assumption that the log ratio is a pertinent quantity to assess the probe status is not always veri.ed and it leads to a poor data interpretation. RESULTS: Instead of working on the log ratio, we directly work with the Ip and Input signals of each probe by modeling the distribution of the Ip signal conditional to the Input signal. We propose a method named ChIPmix based on a linear regression mixture model to identify actual binding targets of the protein under study. Moreover, we are able to control the proportion of false positives. The efficiency of ChIPmix is illustrated on several datasets obtained from different organisms and hybridized either on tiling or promoter arrays. This validation shows that ChIPmix is convenient for any two-color array whatever its density and provides promising results. AVAILABILITY: The ChIPmix method is implemented in R and is available at http://www.agroparistech.fr/mia/outil_A.html.
机译:动机:染色质免疫沉淀(ChIP)与DNA微阵列相结合是一项高通量技术,用于研究DNA-蛋白质结合或染色质/组蛋白修饰。 ChIP芯片数据需要经过调整的统计方法,以识别富集区域。已经提出的所有方法均基于对数比(Ip /输入)的分析。然而,并不总是证实对数比是评估探针状态的相关量的假设,这会导致不良的数据解释。结果:我们不用对数比工作,而是通过对有条件的Ip信号的分布进行建模来直接处理每个探头的Ip和Input信号。我们提出了一种基于线性回归混合物模型的名为ChIPmix的方法,以鉴定所研究蛋白质的实际结合靶标。而且,我们能够控制假阳性的比例。 ChIPmix的效率在从不同生物体获得并在平铺或启动子阵列上杂交的几个数据集中得到了说明。该验证表明,无论其密度如何,ChIPmix均可用于任何两色阵列,并提供了可喜的结果。可用性:ChIPmix方法在R中实现,可以从http://www.agroparistech.fr/mia/outil_A.html获得。

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