眼组织微阵列表达谱研究中生物分析仪电泳质量控制和靶标评价的应用。

Christina A Harrington, Michael Winther, Michelle M Garred
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引用次数: 11

摘要

DNA微阵列表达谱已被用于检查广泛的脊椎动物细胞和组织的转录组。生成的数据的灵敏度和准确性取决于输入RNA的质量和组成。在本报告中,我们检查了从眼部组织和细胞中提取的200多个总RNA样本的质量和阵列性能,这些样本已在微阵列核心实验室处理了7年多的时间。使用2100生物分析仪评估总RNA完整性和cRNA靶大小分布。我们提出Affymetrix基因芯片阵列性能指标,根据标准微阵列分析工作流程处理不同的眼部样品,包括几个质量控制检查点。我们在微阵列分析中对眼部样本性能的回顾证明了在评估阵列数据时考虑组织特异性特征的价值。具体来说,我们表明生物分析仪的电泳图显示泪腺靶标中高度丰富的mrna,这些mrna与阵列分析性能的变化相关。我们的结果为其他眼部系统的基因表达研究提供了有用的基准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Use of bioanalyzer electropherograms for quality control and target evaluation in microarray expression profiling studies of ocular tissues.

Use of bioanalyzer electropherograms for quality control and target evaluation in microarray expression profiling studies of ocular tissues.

Use of bioanalyzer electropherograms for quality control and target evaluation in microarray expression profiling studies of ocular tissues.

Use of bioanalyzer electropherograms for quality control and target evaluation in microarray expression profiling studies of ocular tissues.

Expression profiling with DNA microarrays has been used to examine the transcriptome of a wide spectrum of vertebrate cells and tissues. The sensitivity and accuracy of the data generated is dependent on the quality and composition of the input RNA. In this report, we examine the quality and array performance of over 200 total RNA samples extracted from ocular tissues and cells that have been processed in a microarray core laboratory over a 7-year period. Total RNA integrity and cRNA target size distribution were assessed using the 2100 Bioanalyzer. We present Affymetrix GeneChip array performance metrics for different ocular samples processed according to a standard microarray assay workflow including several quality control checkpoints. Our review of ocular sample performance in the microarray assay demonstrates the value of considering tissue-specific characteristics in evaluating array data. Specifically, we show that Bioanalyzer electropherograms reveal highly abundant mRNAs in lacrimal gland targets that are correlated with variation in array assay performance. Our results provide useful benchmarks for other gene expression studies of ocular systems.

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