Evidence map›Paper›PMID 38515040›Full record

ArticleBMC genomics2024

GNNMF: a multi-view graph neural network for ATAC-seq motif finding.

Shuangquan Zhang, Xiaotian Wu, Zhichao Lian, Chunman Zuo, Yan Wang

Abstract read
In one paragraph

Article in BMC genomics, 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

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Shuangquan ZhangSchool of Cyber Science and Engineering, Nanjing University of Science and Technology, Nanjing, 210094, China.
Xiaotian WuSchool of Artificial Intelligence, Jilin University, Changchun, 130012, China.
Zhichao LianSchool of Cyber Science and Engineering, Nanjing University of Science and Technology, Nanjing, 210094, China. lzcts@163.com.
Chunman ZuoInstitute of Artificial Intelligence, Donghua University, Shanghai, 201620, China.
Yan WangSchool of Artificial Intelligence, Jilin University, Changchun, 130012, China. wy6868@jlu.edu.cn.

Funding

National Natural Science Foundation of China 32300523National Natural Science Foundation of China 62302218
6 · The paper itself

Abstract

backgroundThe Assay for Transposase-Accessible Chromatin using sequencing (ATAC-seq) utilizes the Transposase Tn5 to probe open chromatic, which simultaneously reveals multiple transcription factor binding sites (TFBSs) compared to traditional technologies. Deep learning (DL) technology, including convolutional neural networks (CNNs), has successfully found motifs from ATAC-seq data. Due to the limitation of the width of convolutional kernels, the existing models only find motifs with fixed lengths. A Graph neural network (GNN) can work on non-Euclidean data, which has the potential to find ATAC-seq motifs with different lengths. However, the existing GNN models ignored the relationships among ATAC-seq sequences, and their parameter settings should be improved.

resultsIn this study, we proposed a novel GNN model named GNNMF to find ATAC-seq motifs via GNN and background coexisting probability. Our experiment has been conducted on 200 human datasets and 80 mouse datasets, demonstrated that GNNMF has improved the area of eight metrics radar scores of 4.92% and 6.81% respectively, and found more motifs than did the existing models.

conclusionsIn this study, we developed a novel model named GNNMF for finding multiple ATAC-seq motifs. GNNMF built a multi-view heterogeneous graph by using ATAC-seq sequences, and utilized background coexisting probability and the iterloss to find different lengths of ATAC-seq motifs and optimize the parameter sets. Compared to existing models, GNNMF achieved the best performance on TFBS prediction and ATAC-seq motif finding, which demonstrates that our improvement is available for ATAC-seq motif finding.

Indexed as

Chromatin Immunoprecipitation SequencingHigh-Throughput Nucleotide SequencingAnimalsChromatinHumansMiceNeural Networks, ComputerSequence Analysis, DNAChromatinATAC-seq motifsCoexisting probabilityGraph neural networkMulti-view heterogeneous graph

Identifiers

PMID38515040
PMCPMC10956247

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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.