Evidence map›Paper›PMID 39690881›Full record

ArticleBriefings in bioinformatics2024

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

Junwei Luo, Jiaojiao Wang, Jingjing Wei, Chaokun Yan, Huimin Luo

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Junwei LuoSchool of Software, Henan Polytechnic University, Century Road 2001, Jiaozuo 454003, China.ORCID 0000-0001-6841-9893
Jiaojiao WangSchool of Software, Henan Polytechnic University, Century Road 2001, Jiaozuo 454003, China.
Jingjing WeiCollege of Chemical and Environmental Engineering, Anyang Institute of Technology, West Section of Huanghe Avenue, Anyang 455000, China.
Chaokun YanSchool of Computer and Information Engineering, Henan University, North Section of Jinming Avenue, Kaifeng 475001, China.ORCID 0000-0002-6246-7242
Huimin LuoSchool of Computer and Information Engineering, Henan University, North Section of Jinming Avenue, Kaifeng 475001, China.ORCID 0000-0002-5066-5372

Funding

Henan Provincial Department of Science and Technology Research Project 232102211046Innovative Research Team of Henan Polytechnic University T2021-3National Natural Science Foundation of China 62372156
6 · The paper itself

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.

Indexed as

HaplotypesPolymorphism, Single NucleotideAlgorithmsCluster AnalysisComputational BiologyHigh-Throughput Nucleotide SequencingHumansSequence Analysis, DNASoftwarehaplotype assemblysingle-nucleotide polymorphismsunsupervised learning

Identifiers

PMID39690881
PMCPMC11652615

What OpenQuestion holds

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LicenceCC BY-NC
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.