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AccuTyping: new algorithms for automated analysis of data from high-throughput genotyping with oligonucleotide microarrays

机译:AccuTyping:利用寡核苷酸微阵列自动分析高通量基因分型数据的新算法

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摘要

Microarray-based analysis of single nucleotide polymorphisms (SNPs) has many applications in large-scale genetic studies. To minimize the influence of experimental variation, microarray data usually need to be processed in different aspects including background subtraction, normalization and low-signal filtering before genotype determination. Although many algorithms are sophisticated for these purposes, biases are still present. In the present paper, new algorithms for SNP microarray data analysis and the software, AccuTyping, developed based on these algorithms are described. The algorithms take advantage of a large number of SNPs included in each assay, and the fact that the top and bottom 20% of SNPs can be safely treated as homozygous after sorting based on their ratios between the signal intensities. These SNPs are then used as controls for color channel normalization and background subtraction. Genotype calls are made based on the logarithms of signal intensity ratios using two cutoff values, which were determined after training the program with a dataset of ∼160 000 genotypes and validated by non-microarray methods. AccuTyping was used to determine >300 000 genotypes of DNA and sperm samples. The accuracy was shown to be >99%. AccuTyping can be downloaded from .
机译:基于微阵列的单核苷酸多态性(SNP)分析在大规模遗传研究中有许多应用。为了最大程度地减少实验变异的影响,在确定基因型之前,通常需要在不同方面处理微阵列数据,包括背景扣除,归一化和低信号过滤。尽管许多算法针对这些目的很复杂,但仍然存在偏差。本文介绍了用于SNP微阵列数据分析的新算法以及基于这些算法开发的软件AccuTyping。该算法利用了每个测定中包含的大量SNP,并且可以根据其信号强度之间的比率在排序后将顶部和底部20%的SNP安全地视为纯合子。然后将这些SNP用作颜色通道归一化和背景扣除的控件。基于信号强度比的对数,使用两个截断值进行基因型调用,这是在使用约160 000个基因型数据集训练程序后确定的,并通过非微阵列方法进行了验证。 AccuTyping用于确定DNA和精子样品的> 300 000基因型。准确度显示为> 99%。可以从下载AccuTyping。

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