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Detection of chromosome structural variation by targeted next-generation sequencing and a deep learning application

机译:通过靶向下一代测序和深度学习应用检测染色体结构变异

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摘要

Molecular testing is increasingly important in cancer diagnosis. Targeted next generation sequencing (NGS) is widely accepted method but structural variation (SV) detection by targeted NGS remains challenging. In the brain tumor, identification of molecular alterations, including 1p/19q co-deletion, is essential for accurate glial tumor classification. Hence, we used targeted NGS to detect 1p/19q co-deletion using a newly developed deep learning (DL) model in 61 tumors, including 19 oligodendroglial tumors. An ensemble 1-dimentional convolution neural network was developed and used to detect the 1p/19q co-deletion. External validation was performed using 427 low-grade glial tumors from The Cancer Genome Atlas (TCGA). Manual review of the copy number plot from the targeted NGS identified the 1p/19q co-deletion in all 19 oligodendroglial tumors. Our DL model also perfectly detected the 1p/19q co-deletion (area under the curve, AUC = 1) in the testing set, and yielded reproducible results (AUC = 0.9652) in the validation set (n = 427), although the validation data were generated on a completely different platform (SNP Array 6.0 platform). In conclusion, targeted NGS using a cancer gene panel is a promising approach for classifying glial tumors, and DL can be successfully integrated for the SV detection in NGS data.
机译:分子检测在癌症诊断中越来越重要。有针对性的下一代测序(NGS)是被广泛接受的方法,但是有针对性的NGS检测结构变异(SV)仍然具有挑战性。在脑肿瘤中,鉴定包括1p / 19q共缺失在内的分子改变对于准确的神经胶质瘤分类至关重要。因此,我们使用新开发的深度学习(DL)模型,使用靶向NGS检测1p / 19q共缺失,检测了61种肿瘤,其中包括19种少突胶质细胞瘤。开发了集成的一维卷积神经网络,并将其用于检测1p / 19q共删除。使用来自The Cancer Genome Atlas(TCGA)的427种低度神经胶质瘤进行了外部验证。从目标NGS手动检查拷贝数图可确定在所有19个少突胶质细胞瘤中均存在1p / 19q共缺失。我们的DL模型还完美地检测了测试集中的1p / 19q共缺失(曲线下面积,AUC = 1),并且在验证集中(n = 427)产生了可再现的结果(AUC = 0.9652),尽管验证数据是在完全不同的平台(SNP Array 6.0平台)上生成的。总之,使用癌症基因组靶向NGS是对神经胶质瘤进行分类的一种有前途的方法,并且DL可以成功整合到NGS数据中的SV检测中。

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