A learned comparative expression measure for affymetrix genechip DNA microarrays.

Will Sheffler, Eli Upfal, John Sedivy, William Stafford Noble
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引用次数: 8

Abstract

Perhaps the most common question that a microarray study can ask is, "Between two given biological conditions, which genes exhibit changed expression levels?" Existing methods for answering this question either generate a comparative measure based upon a static model, or take an indirect approach, first estimating absolute expression levels and then comparing the estimated levels to one another. We present a method for detecting changes in gene expression between two samples based on data from Affymetrix GeneChips. Using a library of over 200,000 known cases of differential expression, we create a learned comparative expression measure (LCEM) based on classification of probe-level data patterns as changed or unchanged. LCEM uses perfect match probe data only; mismatch probe values did not prove to be useful in this context. LCEM is particularly powerful in the case of small microarry studies, in which a regression-based method such as RMA cannot generalize, and in detecting small expression changes. At the levels of selectivity that are typical in microarray analysis, the LCEM shows a lower false discovery rate than either MAS5 or RMA trained from a single chip. When many chips are available to RMA, LCEM performs better on two out of the three data sets, and nearly as well on the third. Performance of the MAS5 log ratio statistic was notably bad on all datasets.

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affymetrix基因芯片DNA微阵列的学习比较表达测量。
也许微阵列研究最常见的问题是,“在两种给定的生物条件下,哪些基因表现出表达水平的变化?”回答这个问题的现有方法要么基于静态模型生成比较度量,要么采用间接方法,首先估计绝对表达水平,然后将估计的水平相互比较。我们提出了一种基于Affymetrix GeneChips的数据检测两个样本之间基因表达变化的方法。使用一个包含超过200,000个已知差分表达案例的库,我们基于对探针级数据模式的分类(更改或未更改)创建了一个学习的比较表达度量(LCEM)。LCEM只使用完全匹配的探针数据;在这种情况下,不匹配探测值没有被证明是有用的。LCEM在小型微阵列研究中尤其强大,在这种情况下,基于回归的方法(如RMA)无法推广,并且可以检测小的表达变化。在微阵列分析中典型的选择性水平上,LCEM显示出比单芯片训练的MAS5或RMA更低的错误发现率。当RMA可以使用许多芯片时,LCEM在三个数据集中的两个上表现更好,在第三个数据集上表现也差不多。MAS5对数比率统计的性能在所有数据集上都很差。
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