DeepHapNet: a haplotype assembly method based on RetNet and deep spectral clustering.

IF 6.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS Briefings in bioinformatics Pub Date : 2024-11-22 DOI:10.1093/bib/bbae656
Junwei Luo, Jiaojiao Wang, Jingjing Wei, Chaokun Yan, Huimin Luo
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Abstract

Gene polymorphism originates from single-nucleotide polymorphisms (SNPs), and the analysis and study of SNPs are of great significance in the field of biogenetics. The haplotype, which consists of the sequence of SNP loci, carries more genetic information than a single SNP. Haplotype assembly plays a significant role in understanding gene function, diagnosing complex diseases, and pinpointing species genes. We propose a novel method, DeepHapNet, for haplotype assembly through the clustering of reads and learning correlations between read pairs. We employ a sequence model called Retentive Network (RetNet), which utilizes a multiscale retention mechanism to extract read features and learn the global relationships among them. Based on the feature representation of reads learned from the RetNet model, the clustering process of reads is implemented using the SpectralNet model, and, finally, haplotypes are constructed based on the read clusters. Experiments with simulated and real datasets show that the method performs well in the haplotype assembly problem of diploid and polyploid based on either long or short reads. The code implementation of DeepHapNet and the processing scripts for experimental data are publicly available at https://github.com/wjj6666/DeepHapNet.

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DeepHapNet:基于RetNet和深度谱聚类的单倍型组装方法。
基因多态性起源于单核苷酸多态性(single-nucleotide polymorphisms, SNPs),对其进行分析和研究在生物遗传学领域具有重要意义。单倍型由SNP位点序列组成,比单个SNP携带更多的遗传信息。单倍型组装在了解基因功能、诊断复杂疾病和精确定位物种基因方面发挥着重要作用。我们提出了一种新的方法,DeepHapNet,通过聚类读取和学习读取对之间的相关性来进行单倍型组装。我们采用了一种称为RetNet的序列模型,该模型利用多尺度保留机制提取读特征并学习它们之间的全局关系。在RetNet模型学习到的reads特征表示的基础上,利用SpectralNet模型实现reads聚类过程,最后基于读聚类构建单倍型。实验结果表明,该方法在二倍体和多倍体的长、短序列单倍型装配问题上都有较好的效果。DeepHapNet的代码实现和实验数据的处理脚本可在https://github.com/wjj6666/DeepHapNet上公开获取。
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来源期刊
Briefings in bioinformatics
Briefings in bioinformatics 生物-生化研究方法
CiteScore
13.20
自引率
13.70%
发文量
549
审稿时长
6 months
期刊介绍: Briefings in Bioinformatics is an international journal serving as a platform for researchers and educators in the life sciences. It also appeals to mathematicians, statisticians, and computer scientists applying their expertise to biological challenges. The journal focuses on reviews tailored for users of databases and analytical tools in contemporary genetics, molecular and systems biology. It stands out by offering practical assistance and guidance to non-specialists in computerized methodologies. Covering a wide range from introductory concepts to specific protocols and analyses, the papers address bacterial, plant, fungal, animal, and human data. The journal's detailed subject areas include genetic studies of phenotypes and genotypes, mapping, DNA sequencing, expression profiling, gene expression studies, microarrays, alignment methods, protein profiles and HMMs, lipids, metabolic and signaling pathways, structure determination and function prediction, phylogenetic studies, and education and training.
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