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首页> 外文期刊>BMC Bioinformatics >A verification protocol for the probe sequences of Affymetrix genome arrays reveals high probe accuracy for studies in mouse, human and rat
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A verification protocol for the probe sequences of Affymetrix genome arrays reveals high probe accuracy for studies in mouse, human and rat

机译:Affymetrix基因组阵列探针序列的验证协议揭示了在小鼠,人类和大鼠中进行研究的高探针准确性

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Background The Affymetrix GeneChip technology uses multiple probes per gene to measure its expression level. Individual probe signals can vary widely, which hampers proper interpretation. This variation can be caused by probes that do not properly match their target gene or that match multiple genes. To determine the accuracy of Affymetrix arrays, we developed an extensive verification protocol, for mouse arrays incorporating the NCBI RefSeq, NCBI UniGene Unique, NIA Mouse Gene Index, and UCSC mouse genome databases. Results Applying this protocol to Affymetrix Mouse Genome arrays (the earlier U74Av2 and the newer 430 2.0 array), the number of sequence-verified probes with perfect matches was no less than 85% and 95%, respectively; and for 74% and 85% of the probe sets all probes were sequence verified. The latter percentages increased to 80% and 94% after discarding one or two unverifiable probes per probe set, and even further to 84% and 97% when, in addition, allowing for one or two mismatches between probe and target gene. Similar results were obtained for other mouse arrays, as well as for human and rat arrays. Based on these data, refined chip definition files for all arrays are provided online. Researchers can choose the version appropriate for their study to (re)analyze expression data. Conclusion The accuracy of Affymetrix probe sequences is higher than previously reported, particularly on newer arrays. Yet, refined probe set definitions have clear effects on the detection of differentially expressed genes. We demonstrate that the interpretation of the results of Affymetrix arrays is improved when the new chip definition files are used.
机译:背景技术Affymetrix GeneChip技术使用每个基因多个探针来测量其表达水平。各个探测信号可能相差很大,这会妨碍正确的解释。这种变异可能是由与目标基因不正确匹配或与多个基因匹配的探针引起的。为了确定Affymetrix阵列的准确性,我们针对包含NCBI RefSeq,NCBI UniGene Unique,NIA小​​鼠基因索引和UCSC小鼠基因组数据库的鼠标阵列开发了广泛的验证协议。结果将该协议应用于Affymetrix小鼠基因组阵列(较早的U74Av2和较新的430 2.0阵列),具有完美匹配的序列验证探针的数量分别不少于85%和95%;对于74%和85%的探针组,所有探针均经过序列验证。在丢弃每个探针组一个或两个不可验证的探针后,后者的百分比增加到80%和94%,此外,如果允许探针和目标基因之间存在一两个错配,则进一步增加到84%和97%。其他鼠标阵列以及人和大鼠阵列也获得了类似的结果。基于这些数据,可以在线提供所有阵列的精确芯片定义文件。研究人员可以选择适合其研究的版本来(重新)分析表达数据。结论Affymetrix探针序列的准确性比以前报道的要高,尤其是在较新的阵列上。然而,完善的探针组定义对差异表达基因的检测具有明显的影响。我们证明,使用新的芯片定义文件时,Affymetrix阵列结果的解释会得到改善。

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