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Translating Quantitative Proteomics Data into Biological Insight: Methodology for Replicate Proteomics Data Analysis in the Context of Type 2 Diabetes

机译:将定量蛋白质组学数据转化为生物洞察:2型糖尿病背景下复制蛋白质组学数据分析的方法

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1. We have implemented a prototype algorithm that solves the following: 2. Input: Replicated quan ta ve data from COMPASS, including protein and phospho-isoforms from a high-throughput experiment and a list of comparisons 3. Output: list of signi fi cant measurement-comparison pairs. 4. We have included transcript and microarray quan ta on, allowing us to compare protein with transcript, phospho-isoform with protein, imputed mo fs, and imputed kinases. 5. We effi ciently perform 39 biologically meaningful comparisons on 89,584 measurements, for a total of 3.5 million measurement-comparisons. 6. We found 101,402 signifi cant measurement-comparisons (3% of possible) (10% FDR) 7. We found that 9,314 measurements changed signifi cantly in some comparison (10% of possible) (10% FDR). 8. We have started verifying biologically relevant results discovered using this data.
机译:1.我们已经实现了一种原型算法,解决了以下内容:2。输入:从罗盘复制的Quan Ta VE数据,包括来自高通量实验的蛋白质和磷酸同种型和比较列表3.输出:意义列表列表无法测量 - 比较对。我们已经包括转录物和微阵列Quan TA,允许我们将蛋白质与转录物,磷酸同种型与蛋白质,闭塞的Mo Fs和避税激酶进行比较。 5.我们在89,584次测量中产生了39种生物学有意义的比较,总计350万测量 - 比较。 6.我们发现了101,402个标志性的测量 - 比较 - 比较(占可能的3%)(10%FDR)7。我们发现9,314次测量在一些比较(占可能的10%)(10%FDR)(10%FDR)的情况下显着改变了Signifi。 8.我们已经开始验证使用此数据发现的生物学相关结果。

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