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Evaluating the influence of quality control decisions and software algorithms on SNP calling for the affymetrix 6.0 SNP array platform.

机译:评估质量控制决策和软件算法对SNP的影响,从而需要affymetrix 6.0 SNP阵列平台。

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摘要

Objective: Our goal was to evaluate the influence of quality control (QC) decisions using two genotype calling algorithms, CRLMM and Birdseed, designed for the Affymetrix SNP Array 6.0. Methods: Various QC options were tried using the two algorithms and comparisons were made on subject and call rate and on association results using two data sets. Results: For Birdseed, we recommend using the contrast QC instead of QC call rate for sample QC. For CRLMM, we recommend using the signal-to-noise rate >/=4 for sample QC and a posterior probability of 90% for genotype accuracy. For both algorithms, we recommend calling the genotype separately for each plate, and dropping SNPs with a lower call rate (<95%) before evaluating samples with lower call rates. To investigate whether the genotype calls from the two algorithms impacted the genome-wide association results, we performed association analysis using data from the GENOA cohort; we observed that the number of significant SNPs were similar using either CRLMM or Birdseed. Conclusions: Using our suggested workflow both algorithms performed similarly; however, fewer samples were removed and CRLMM took half the time to run our 854 study samples (4.2 h) compared to Birdseed (8.4 h).
机译:目的:我们的目标是使用为Affymetrix SNP Array 6.0设计的两种基因型调用算法CRLMM和Birdseed评估质量控制(QC)决策的影响。方法:使用这两种算法尝试了各种质量控制选项,并使用两个数据集对主题和通话率以及关联结果进行了比较。结果:对于Birdseed,我们建议使用对比质量控制代替样品质量控制的质量控制调用率。对于CRLMM,我们建议对样品QC使用信噪比> / = 4,对基因型准确性使用90%的后验概率。对于这两种算法,我们建议为每个板分别调用基因型,并在评估具有较低检出率的样品之前,以较低的检出率(<95%)丢弃SNP。为了研究这两种算法的基因型调用是否影响全基因组关联结果,我们使用了来自GENOA队列的数据进行了关联分析。我们观察到,使用CRLMM或Birdseed,重要SNP的数量相似。结论:使用我们建议的工作流程,两种算法的执行效果相似。但是,与Birdseed(8.4小时)相比,CRLMM减少了一半的样品运行时间(4.2小时)来运行我们的854个研究样品。

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