利用深度学习模型通过图像处理进行基因组分析。

IF 2.6 3区 生物学 Q2 GENETICS & HEREDITY
Yao-zhong Zhang, Seiya Imoto
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引用次数: 0

摘要

基因组序列传统上用字符串表示:A(腺嘌呤)、C(胞嘧啶)、G(鸟嘌呤)和 T(胸腺嘧啶)。然而,另一种方法是通过图像表示法来描述序列相关信息,如混沌博弈表示法(CGR)和读取堆积图像。随着计算机视觉和自然语言处理领域深度学习(DL)方法的快速发展,将基于图像的 DL 方法应用于基因组序列分析的兴趣日益浓厚。这些方法涉及将基因组信息编码为图像,或将图像中的空间信息整合到分析过程中。在本综述中,我们总结了将图像处理与 DL 模型用于基因组分析的三种典型应用。我们研究了这些基于图像的方法的使用情况和优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Genome analysis through image processing with deep learning models

Genome analysis through image processing with deep learning models

Genome analysis through image processing with deep learning models
Genomic sequences are traditionally represented as strings of characters: A (adenine), C (cytosine), G (guanine), and T (thymine). However, an alternative approach involves depicting sequence-related information through image representations, such as Chaos Game Representation (CGR) and read pileup images. With rapid advancements in deep learning (DL) methods within computer vision and natural language processing, there is growing interest in applying image-based DL methods to genomic sequence analysis. These methods involve encoding genomic information as images or integrating spatial information from images into the analytical process. In this review, we summarize three typical applications that use image processing with DL models for genome analysis. We examine the utilization and advantages of these image-based approaches.
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来源期刊
Journal of Human Genetics
Journal of Human Genetics 生物-遗传学
CiteScore
7.20
自引率
0.00%
发文量
101
审稿时长
4-8 weeks
期刊介绍: The Journal of Human Genetics is an international journal publishing articles on human genetics, including medical genetics and human genome analysis. It covers all aspects of human genetics, including molecular genetics, clinical genetics, behavioral genetics, immunogenetics, pharmacogenomics, population genetics, functional genomics, epigenetics, genetic counseling and gene therapy. Articles on the following areas are especially welcome: genetic factors of monogenic and complex disorders, genome-wide association studies, genetic epidemiology, cancer genetics, personal genomics, genotype-phenotype relationships and genome diversity.
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