Challenges for machine learning in RNA-protein interaction prediction.

IF 0.9 4区 数学 Q3 Mathematics Statistical Applications in Genetics and Molecular Biology Pub Date : 2022-05-02 DOI:10.1515/sagmb-2021-0087
Viplove Arora, Guido Sanguinetti
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引用次数: 1

Abstract

RNA-protein interactions have long being recognised as crucial regulators of gene expression. Recently, the development of scalable experimental techniques to measure these interactions has revolutionised the field, leading to the production of large-scale datasets which offer both opportunities and challenges for machine learning techniques. In this brief note, we will discuss some of the major stumbling blocks towards the use of machine learning in computational RNA biology, focusing specifically on the problem of predicting RNA-protein interactions from next-generation sequencing data.

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机器学习在rna -蛋白相互作用预测中的挑战。
长期以来,rna -蛋白相互作用一直被认为是基因表达的关键调控因子。最近,测量这些相互作用的可扩展实验技术的发展已经彻底改变了该领域,导致大规模数据集的产生,这为机器学习技术提供了机遇和挑战。在这篇简短的文章中,我们将讨论在计算RNA生物学中使用机器学习的一些主要障碍,特别关注从下一代测序数据预测RNA-蛋白质相互作用的问题。
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来源期刊
CiteScore
1.20
自引率
11.10%
发文量
8
审稿时长
6-12 weeks
期刊介绍: Statistical Applications in Genetics and Molecular Biology seeks to publish significant research on the application of statistical ideas to problems arising from computational biology. The focus of the papers should be on the relevant statistical issues but should contain a succinct description of the relevant biological problem being considered. The range of topics is wide and will include topics such as linkage mapping, association studies, gene finding and sequence alignment, protein structure prediction, design and analysis of microarray data, molecular evolution and phylogenetic trees, DNA topology, and data base search strategies. Both original research and review articles will be warmly received.
期刊最新文献
Empirically adjusted fixed-effects meta-analysis methods in genomic studies. A CNN-CBAM-BIGRU model for protein function prediction. A heavy-tailed model for analyzing miRNA-seq raw read counts. Flexible model-based non-negative matrix factorization with application to mutational signatures. Choice of baseline hazards in joint modeling of longitudinal and time-to-event cancer survival data.
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