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DeepMILO: a deep learning approach to predict the impact of non-coding sequence variants on 3D chromatin structure

机译:DeepMilo:一种深入的学习方法,可以预测非编码序列变体对3D染色质结构的影响

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Non-coding variants have been shown to be related to disease by alteration of 3D genome structures. We propose a deep learning method, DeepMILO, to predict the effects of variants on CTCF/cohesin-mediated insulator loops. Application of DeepMILO on variants from whole-genome sequences of 1834 patients of twelve cancer types revealed 672 insulator loops disrupted in at least 10% of patients. Our results show mutations at loop anchors are associated with upregulation of the cancer driver genes BCL2 and MYC in malignant lymphoma thus pointing to a possible new mechanism for their dysregulation via alteration of insulator loops.
机译:通过改变3D基因组结构,已显示非编码变体与疾病有关。我们提出了一种深入的学习方法,Deepmilo,预测变体对CTCF / Cohyin介导的绝缘子环的影响。 Deepmilo在1834名癌症类型患者的全基因组序列中的应用揭示了至少10%的患者中断的672个绝缘子环。我们的结果显示环锚的突变与恶性淋巴瘤的癌症驱动基因Bcl2和MyC的上调相关,从而指向通过抑制绝缘体环的癌细胞的可能性新机制。

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