Deep transformers and convolutional neural network in identifying DNA N6-methyladenine sites in cross-species genomes
[Display omitted] •A novel model for identifying DNA N6-methyladenine sites in cross-species genomes.•Transformers-based BERT pretrained model is used to extract features from DNA sequences.•Deep convolutional neural network is employed and optimized to learn features.•The model is superior to previ...
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Veröffentlicht in: | Methods (San Diego, Calif.) Calif.), 2022-08, Vol.204, p.199-206 |
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creator | Le, Nguyen Quoc Khanh Ho, Quang-Thai |
description | [Display omitted]
•A novel model for identifying DNA N6-methyladenine sites in cross-species genomes.•Transformers-based BERT pretrained model is used to extract features from DNA sequences.•Deep convolutional neural network is employed and optimized to learn features.•The model is superior to previous models on the same problem/data.
As one of the most common post-transcriptional epigenetic modifications, N6-methyladenine (6 mA), plays an essential role in various cellular processes and disease pathogenesis. Therefore, accurately identifying 6 mA modifications is necessary for a deep understanding of cellular processes and other possible functional mechanisms. Although a few computational methods have been proposed, their respective models were developed with small training datasets. Hence, their practical application is quite limited in genome-wide detection. To overcome the existing limitations, we present a novel model based on transformer architecture and deep learning to identify DNA 6 mA sites from the cross-species genome. The model is constructed on a benchmark dataset and explored a feature derived from pre-trained transformer word embedding approaches. Subsequently, a convolutional neural network was employed to learn the generated features and generate the prediction outcomes. As a result, our predictor achieved excellent performance during independent test with the accuracy and Matthews correlation coefficient (MCC) of 79.3% and 0.58, respectively. Overall, its performance achieved better accuracy than the baseline models and significantly outperformed the existing predictors, demonstrating the effectiveness of our proposed hybrid framework. Furthermore, our model is expected to assist biologists in accurately identifying 6mAs and formulate the novel testable biological hypothesis. We also release source codes and datasets freely at https://github.com/khanhlee/bert-dna for front-end users. |
doi_str_mv | 10.1016/j.ymeth.2021.12.004 |
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•A novel model for identifying DNA N6-methyladenine sites in cross-species genomes.•Transformers-based BERT pretrained model is used to extract features from DNA sequences.•Deep convolutional neural network is employed and optimized to learn features.•The model is superior to previous models on the same problem/data.
As one of the most common post-transcriptional epigenetic modifications, N6-methyladenine (6 mA), plays an essential role in various cellular processes and disease pathogenesis. Therefore, accurately identifying 6 mA modifications is necessary for a deep understanding of cellular processes and other possible functional mechanisms. Although a few computational methods have been proposed, their respective models were developed with small training datasets. Hence, their practical application is quite limited in genome-wide detection. To overcome the existing limitations, we present a novel model based on transformer architecture and deep learning to identify DNA 6 mA sites from the cross-species genome. The model is constructed on a benchmark dataset and explored a feature derived from pre-trained transformer word embedding approaches. Subsequently, a convolutional neural network was employed to learn the generated features and generate the prediction outcomes. As a result, our predictor achieved excellent performance during independent test with the accuracy and Matthews correlation coefficient (MCC) of 79.3% and 0.58, respectively. Overall, its performance achieved better accuracy than the baseline models and significantly outperformed the existing predictors, demonstrating the effectiveness of our proposed hybrid framework. Furthermore, our model is expected to assist biologists in accurately identifying 6mAs and formulate the novel testable biological hypothesis. We also release source codes and datasets freely at https://github.com/khanhlee/bert-dna for front-end users.</description><identifier>ISSN: 1046-2023</identifier><identifier>EISSN: 1095-9130</identifier><identifier>DOI: 10.1016/j.ymeth.2021.12.004</identifier><identifier>PMID: 34915158</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Contextualized word embedding ; Deep learning ; DNA sequence analysis ; N6-methyladenine site ; Natural language processing ; Post-translational modification</subject><ispartof>Methods (San Diego, Calif.), 2022-08, Vol.204, p.199-206</ispartof><rights>2021 Elsevier Inc.</rights><rights>Copyright © 2021 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-89f8d84f28988bb1493d7db3ee6311ff0c740ad5e1b3bf2aaad103be5da354c43</citedby><cites>FETCH-LOGICAL-c359t-89f8d84f28988bb1493d7db3ee6311ff0c740ad5e1b3bf2aaad103be5da354c43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1046202321002747$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34915158$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Le, Nguyen Quoc Khanh</creatorcontrib><creatorcontrib>Ho, Quang-Thai</creatorcontrib><title>Deep transformers and convolutional neural network in identifying DNA N6-methyladenine sites in cross-species genomes</title><title>Methods (San Diego, Calif.)</title><addtitle>Methods</addtitle><description>[Display omitted]
•A novel model for identifying DNA N6-methyladenine sites in cross-species genomes.•Transformers-based BERT pretrained model is used to extract features from DNA sequences.•Deep convolutional neural network is employed and optimized to learn features.•The model is superior to previous models on the same problem/data.
As one of the most common post-transcriptional epigenetic modifications, N6-methyladenine (6 mA), plays an essential role in various cellular processes and disease pathogenesis. Therefore, accurately identifying 6 mA modifications is necessary for a deep understanding of cellular processes and other possible functional mechanisms. Although a few computational methods have been proposed, their respective models were developed with small training datasets. Hence, their practical application is quite limited in genome-wide detection. To overcome the existing limitations, we present a novel model based on transformer architecture and deep learning to identify DNA 6 mA sites from the cross-species genome. The model is constructed on a benchmark dataset and explored a feature derived from pre-trained transformer word embedding approaches. Subsequently, a convolutional neural network was employed to learn the generated features and generate the prediction outcomes. As a result, our predictor achieved excellent performance during independent test with the accuracy and Matthews correlation coefficient (MCC) of 79.3% and 0.58, respectively. Overall, its performance achieved better accuracy than the baseline models and significantly outperformed the existing predictors, demonstrating the effectiveness of our proposed hybrid framework. Furthermore, our model is expected to assist biologists in accurately identifying 6mAs and formulate the novel testable biological hypothesis. We also release source codes and datasets freely at https://github.com/khanhlee/bert-dna for front-end users.</description><subject>Contextualized word embedding</subject><subject>Deep learning</subject><subject>DNA sequence analysis</subject><subject>N6-methyladenine site</subject><subject>Natural language processing</subject><subject>Post-translational modification</subject><issn>1046-2023</issn><issn>1095-9130</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kEtv1DAQgCMEog_4BUjIRy4JHtvJJgcOVUtbpKpc2rPl2OPiJbEX2ynaf4-zWzhyGmvmm4e_qvoAtAEK3edts58x_2gYZdAAaygVr6pToENbD8Dp6_UturqU-Ul1ltKWUgps07-tTrgYoIW2P62WK8QdyVH5ZEOcMSaivCE6-OcwLdkFrybicYmHkH-H-JM4T5xBn53dO_9Eru4vyH1Xr7fsJ1UKziNJLmNaSR1DSnXaoXYl8YQ-zJjeVW-smhK-f4nn1eP114fL2_ru-823y4u7WvN2yHU_2N70wrJ-6PtxBDFwszEjR-w4gLVUbwRVpkUY-WiZUsoA5SO2RvFWaMHPq0_HubsYfi2Yspxd0jhNymNYkmQdQNexQbQF5Uf0cHBEK3fRzSruJVC5-pZbefAtV98SmCy-S9fHlwXLOKP51_NXcAG-HAEs33x2GGUqIrxG4yLqLE1w_13wB1zplQ0</recordid><startdate>20220801</startdate><enddate>20220801</enddate><creator>Le, Nguyen Quoc Khanh</creator><creator>Ho, Quang-Thai</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20220801</creationdate><title>Deep transformers and convolutional neural network in identifying DNA N6-methyladenine sites in cross-species genomes</title><author>Le, Nguyen Quoc Khanh ; Ho, Quang-Thai</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-89f8d84f28988bb1493d7db3ee6311ff0c740ad5e1b3bf2aaad103be5da354c43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Contextualized word embedding</topic><topic>Deep learning</topic><topic>DNA sequence analysis</topic><topic>N6-methyladenine site</topic><topic>Natural language processing</topic><topic>Post-translational modification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Le, Nguyen Quoc Khanh</creatorcontrib><creatorcontrib>Ho, Quang-Thai</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Methods (San Diego, Calif.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Le, Nguyen Quoc Khanh</au><au>Ho, Quang-Thai</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Deep transformers and convolutional neural network in identifying DNA N6-methyladenine sites in cross-species genomes</atitle><jtitle>Methods (San Diego, Calif.)</jtitle><addtitle>Methods</addtitle><date>2022-08-01</date><risdate>2022</risdate><volume>204</volume><spage>199</spage><epage>206</epage><pages>199-206</pages><issn>1046-2023</issn><eissn>1095-9130</eissn><abstract>[Display omitted]
•A novel model for identifying DNA N6-methyladenine sites in cross-species genomes.•Transformers-based BERT pretrained model is used to extract features from DNA sequences.•Deep convolutional neural network is employed and optimized to learn features.•The model is superior to previous models on the same problem/data.
As one of the most common post-transcriptional epigenetic modifications, N6-methyladenine (6 mA), plays an essential role in various cellular processes and disease pathogenesis. Therefore, accurately identifying 6 mA modifications is necessary for a deep understanding of cellular processes and other possible functional mechanisms. Although a few computational methods have been proposed, their respective models were developed with small training datasets. Hence, their practical application is quite limited in genome-wide detection. To overcome the existing limitations, we present a novel model based on transformer architecture and deep learning to identify DNA 6 mA sites from the cross-species genome. The model is constructed on a benchmark dataset and explored a feature derived from pre-trained transformer word embedding approaches. Subsequently, a convolutional neural network was employed to learn the generated features and generate the prediction outcomes. As a result, our predictor achieved excellent performance during independent test with the accuracy and Matthews correlation coefficient (MCC) of 79.3% and 0.58, respectively. Overall, its performance achieved better accuracy than the baseline models and significantly outperformed the existing predictors, demonstrating the effectiveness of our proposed hybrid framework. Furthermore, our model is expected to assist biologists in accurately identifying 6mAs and formulate the novel testable biological hypothesis. We also release source codes and datasets freely at https://github.com/khanhlee/bert-dna for front-end users.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>34915158</pmid><doi>10.1016/j.ymeth.2021.12.004</doi><tpages>8</tpages></addata></record> |
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subjects | Contextualized word embedding Deep learning DNA sequence analysis N6-methyladenine site Natural language processing Post-translational modification |
title | Deep transformers and convolutional neural network in identifying DNA N6-methyladenine sites in cross-species genomes |
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