生物
增强子
计算生物学
功能基因组学
基因组学
调节顺序
遗传学
转录因子
DNA结合位点
基因组
基因
发起人
基因表达
作者
Shengcheng Dong,Alan P. Boyle
出处
期刊:Human Mutation
[Wiley]
日期:2019-09-01
卷期号:40 (9): 1292-1298
被引量:78
摘要
Here we present a computational model, Score of Unified Regulatory Features (SURF), that predicts functional variants in enhancer and promoter elements. SURF is trained on data from massively parallel reporter assays and predicts the effect of variants on reporter expression levels. It achieved the top performance in the Fifth Critical Assessment of Genome Interpretation "Regulation Saturation" challenge. We also show that features queried through RegulomeDB, which are direct annotations from functional genomics data, help improve prediction accuracy beyond transfer learning features from DNA sequence-based deep learning models. Some of the most important features include DNase footprints, especially when coupled with complementary ChIP-seq data. Furthermore, we found our model achieved good performance in predicting allele-specific transcription factor binding events. As an extension to the current scoring system in RegulomeDB, we expect our computational model to prioritize variants in regulatory regions, thus help the understanding of functional variants in noncoding regions that lead to disease.
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