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Whole-genome microarrays of fission yeast: characteristics, accuracy, reproducibility, and processing of array data

机译:裂殖酵母全基因组微阵列:特征,准确性,可重复性和阵列数据处理

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Background: The genome of the fission yeast Schizosaccharomyces pombe has recently been sequenced, setting the stage for the post-genomic era of this increasingly popular model organism. We have built fission yeast microarrays, optimised protocols to improve array performance, and carried out experiments to assess various characteristics of microarrays.|Results: We designed PCR primers to amplify specific probes (180-500 bp) for all known and predicted fission yeast genes, which are printed in duplicate onto separate regions of glass slides together with control elements (similar to13,000 spots/slide). Fluorescence signal intensities depended on the size and intragenic position of the array elements, whereas the signal ratios were largely independent of element properties. Only the coding strand is covalently linked to the slides, and our array elements can discriminate transcriptional direction. The microarrays can distinguish sequences with up to 70% identity, above which cross-hybridisation contributes to the signal intensity. We tested the accuracy of signal ratios and measured the reproducibility of array data caused by biological and technical factors. Because the technical variability is lower, it is best to use samples prepared from independent biological experiments to obtain repeated measurements with swapping of fluorochromes to prevent dye bias. We also developed a script that discards unreliable data and performs a normalization to correct spatial artefacts.|Conclusions: This paper provides data for several microarray properties that are rarely measured. The results define critical parameters for microarray design and experiments and provide a framework to optimise and interpret array data. Our arrays give reproducible and accurate expression ratios with high sensitivity. The scripts for primer design and initial data processing as well as primer sequences and detailed protocols are available from our website.
机译:背景:裂变酵母粟酒裂殖酵母(Schizosaccharomyces pombe)的基因组最近已测序,为这种日益流行的模型生物的后基因组时代奠定了基础。我们已经建立了裂殖酵母微阵列,优化了协议以提高阵列性能,并进行了实验以评估微阵列的各种特征。 ,一式两份地与控制元件一起打印在载玻片的单独区域上(类似于13,000个斑点/载玻片)。荧光信号强度取决于阵列元件的大小和基因内位置,而信号比在很大程度上与元件特性无关。只有编码链与载玻片共价连接,我们的阵列元件可以区分转录方向。微阵列可以区分具有高达70%同一性的序列,高于该序列,交叉杂交有助于信号强度。我们测试了信号比率的准确性,并测量了由生物学和技术因素引起的阵列数据的可重复性。由于技术可变性较低,因此最好使用通过独立生物学实验制备的样品,通过交换荧光染料来进行重复测量,以防止染料偏倚。我们还开发了一个脚本,该脚本可丢弃不可靠的数据并执行归一化以纠正空间伪影。|结论:本文提供了一些很少测量的微阵列特性的数据。结果为微阵列设计和实验定义了关键参数,并提供了优化和解释阵列数据的框架。我们的阵列具有高灵敏度,可再现且准确的表达比例。引物设计和初始数据处理的脚本以及引物序列和详细的协议可从我们的网站上获得。

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