Detecting rare copy number variants from Illumina genotyping arrays with the CamCNV pipeline: Segmentation of z-scores improves detection and reliability.

Detecting rare copy number variants from Illumina genotyping arrays with the CamCNV pipeline: Segmentation of z-scores improves detection and reliability.
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DOI:
10.1002/gepi.22367
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发表时间:
2021-04
影响因子:
2.1
通讯作者:
Easton DF
Easton DF
中科院分区:
医学4区
文献类型:
--
作者:
Dennis J;Walker L;Tyrer J;Michailidou K;Easton DF

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来自基因分型阵列数据的强度可用于检测CNV,但数据中的高水平噪声和不同拷贝数强度分布之间的重叠产生不可靠的调用,特别是当CNV仅覆盖少数探针时。我们提出了一种新的管道(CamCNV),它具有一系列步骤来降低噪声并更可靠地检测覆盖少至三个探针的CNV。该管道旨在检测罕见的CNV(频率低于1%),用于大型队列的关联测试。该方法使用来自所有样品的信息将强度转换为z分数,从而调整探针之间的方差。我们通过在1000个基因组样本的基因分型中寻找来自1000个基因组项目的已知CNV来测试我们的管道的灵敏度。我们还比较了1,661对基因分型重复样本的CNV调用。在选定的平均z分数截止值,检测1000个基因组CNV的灵敏度对于缺失约为85%,对于重复约为65%。从重复中,我们估计缺失的错误发现率控制在约10%(超过5个探针时降至3%以下),重复的错误发现率控制在约28%。与PennCNV调用相比,该管道显示出提高的灵敏度,特别是对于仅覆盖几个探针的短缺失。对于每个调用的CNV,平均z分数是用于控制错误发现率的有用度量。
The intensities from genotyping array data can be used to detect CNVs but a high level of noise in the data and overlap between different copy-number intensity distributions produces unreliable calls, particularly when only a few probes are covered by the CNV. We present a novel pipeline (CamCNV) with a series of steps to reduce noise and detect more reliably CNVs covering as few as three probes. The pipeline aims to detect rare CNVs (below 1% frequency) for association tests in large cohorts. The method uses the information from all samples to convert intensities to z-scores, thus adjusting for variance between probes. We tested the sensitivity of our pipeline by looking for known CNVs from the 1000 Genomes project in our genotyping of 1000 Genomes samples. We also compared the CNV calls for 1,661 pairs of genotyped replicate samples. At the chosen mean z-score cut-off, sensitivity to detect the 1000 Genomes CNVs was approximately 85% for deletions and 65% for duplications. From the replicates we estimate the false discovery rate is controlled at ~10% for deletions (falling to below 3% with more than five probes) and ~28% for duplications. The pipeline demonstrates improved sensitivity when compared to calling with PennCNV, particularly for short deletions covering only a few probes. For each called CNV the mean z-score is a useful metric for controlling the false discovery rate.
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