TEC-miTarget: enhancing microRNA target prediction based on deep learning of ribonucleic acid sequences

MicroRNAs play a critical role in regulating gene expression by binding to specific target sites within gene transcripts, making the identification of microRNA targets a prominent focus of research. Conventional experimental methods for identifying microRNA targets are both time-consuming and expens...

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Published inBMC bioinformatics Vol. 25; no. 1; p. 159
Main Authors Yang, Tingpeng, Wang, Yu, He, Yonghong
Format Journal Article
LanguageEnglish
Published England BioMed Central Ltd 20.04.2024
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Abstract MicroRNAs play a critical role in regulating gene expression by binding to specific target sites within gene transcripts, making the identification of microRNA targets a prominent focus of research. Conventional experimental methods for identifying microRNA targets are both time-consuming and expensive, prompting the development of computational tools for target prediction. However, the existing computational tools exhibit limited performance in meeting the demands of practical applications, highlighting the need to improve the performance of microRNA target prediction models. In this paper, we utilize the most popular natural language processing and computer vision technologies to propose a novel approach, called TEC-miTarget, for microRNA target prediction based on transformer encoder and convolutional neural networks. TEC-miTarget treats RNA sequences as a natural language and encodes them using a transformer encoder, a widely used encoder in natural language processing. It then combines the representations of a pair of microRNA and its candidate target site sequences into a contact map, which is a three-dimensional array similar to a multi-channel image. Therefore, the contact map's features are extracted using a four-layer convolutional neural network, enabling the prediction of interactions between microRNA and its candidate target sites. We applied a series of comparative experiments to demonstrate that TEC-miTarget significantly improves microRNA target prediction, compared with existing state-of-the-art models. Our approach is the first approach to perform comparisons with other approaches at both sequence and transcript levels. Furthermore, it is the first approach compared with both deep learning-based and seed-match-based methods. We first compared TEC-miTarget's performance with approaches at the sequence level, and our approach delivers substantial improvements in performance using the same datasets and evaluation metrics. Moreover, we utilized TEC-miTarget to predict microRNA targets in long mRNA sequences, which involves two steps: selecting candidate target site sequences and applying sequence-level predictions. We finally showed that TEC-miTarget outperforms other approaches at the transcript level, including the popular seed match methods widely used in previous years. We propose a novel approach for predicting microRNA targets at both sequence and transcript levels, and demonstrate that our approach outperforms other methods based on deep learning or seed match. We also provide our approach as an easy-to-use software, TEC-miTarget, at https://github.com/tingpeng17/TEC-miTarget . Our results provide new perspectives for microRNA target prediction.
AbstractList MicroRNAs play a critical role in regulating gene expression by binding to specific target sites within gene transcripts, making the identification of microRNA targets a prominent focus of research. Conventional experimental methods for identifying microRNA targets are both time-consuming and expensive, prompting the development of computational tools for target prediction. However, the existing computational tools exhibit limited performance in meeting the demands of practical applications, highlighting the need to improve the performance of microRNA target prediction models. In this paper, we utilize the most popular natural language processing and computer vision technologies to propose a novel approach, called TEC-miTarget, for microRNA target prediction based on transformer encoder and convolutional neural networks. TEC-miTarget treats RNA sequences as a natural language and encodes them using a transformer encoder, a widely used encoder in natural language processing. It then combines the representations of a pair of microRNA and its candidate target site sequences into a contact map, which is a three-dimensional array similar to a multi-channel image. Therefore, the contact map's features are extracted using a four-layer convolutional neural network, enabling the prediction of interactions between microRNA and its candidate target sites. We applied a series of comparative experiments to demonstrate that TEC-miTarget significantly improves microRNA target prediction, compared with existing state-of-the-art models. Our approach is the first approach to perform comparisons with other approaches at both sequence and transcript levels. Furthermore, it is the first approach compared with both deep learning-based and seed-match-based methods. We first compared TEC-miTarget's performance with approaches at the sequence level, and our approach delivers substantial improvements in performance using the same datasets and evaluation metrics. Moreover, we utilized TEC-miTarget to predict microRNA targets in long mRNA sequences, which involves two steps: selecting candidate target site sequences and applying sequence-level predictions. We finally showed that TEC-miTarget outperforms other approaches at the transcript level, including the popular seed match methods widely used in previous years. We propose a novel approach for predicting microRNA targets at both sequence and transcript levels, and demonstrate that our approach outperforms other methods based on deep learning or seed match. We also provide our approach as an easy-to-use software, TEC-miTarget, at https://github.com/tingpeng17/TEC-miTarget. Our results provide new perspectives for microRNA target prediction.
Abstract Background MicroRNAs play a critical role in regulating gene expression by binding to specific target sites within gene transcripts, making the identification of microRNA targets a prominent focus of research. Conventional experimental methods for identifying microRNA targets are both time-consuming and expensive, prompting the development of computational tools for target prediction. However, the existing computational tools exhibit limited performance in meeting the demands of practical applications, highlighting the need to improve the performance of microRNA target prediction models. Results In this paper, we utilize the most popular natural language processing and computer vision technologies to propose a novel approach, called TEC-miTarget, for microRNA target prediction based on transformer encoder and convolutional neural networks. TEC-miTarget treats RNA sequences as a natural language and encodes them using a transformer encoder, a widely used encoder in natural language processing. It then combines the representations of a pair of microRNA and its candidate target site sequences into a contact map, which is a three-dimensional array similar to a multi-channel image. Therefore, the contact map's features are extracted using a four-layer convolutional neural network, enabling the prediction of interactions between microRNA and its candidate target sites. We applied a series of comparative experiments to demonstrate that TEC-miTarget significantly improves microRNA target prediction, compared with existing state-of-the-art models. Our approach is the first approach to perform comparisons with other approaches at both sequence and transcript levels. Furthermore, it is the first approach compared with both deep learning-based and seed-match-based methods. We first compared TEC-miTarget’s performance with approaches at the sequence level, and our approach delivers substantial improvements in performance using the same datasets and evaluation metrics. Moreover, we utilized TEC-miTarget to predict microRNA targets in long mRNA sequences, which involves two steps: selecting candidate target site sequences and applying sequence-level predictions. We finally showed that TEC-miTarget outperforms other approaches at the transcript level, including the popular seed match methods widely used in previous years. Conclusions We propose a novel approach for predicting microRNA targets at both sequence and transcript levels, and demonstrate that our approach outperforms other methods based on deep learning or seed match. We also provide our approach as an easy-to-use software, TEC-miTarget, at https://github.com/tingpeng17/TEC-miTarget . Our results provide new perspectives for microRNA target prediction.
BACKGROUNDMicroRNAs play a critical role in regulating gene expression by binding to specific target sites within gene transcripts, making the identification of microRNA targets a prominent focus of research. Conventional experimental methods for identifying microRNA targets are both time-consuming and expensive, prompting the development of computational tools for target prediction. However, the existing computational tools exhibit limited performance in meeting the demands of practical applications, highlighting the need to improve the performance of microRNA target prediction models.RESULTSIn this paper, we utilize the most popular natural language processing and computer vision technologies to propose a novel approach, called TEC-miTarget, for microRNA target prediction based on transformer encoder and convolutional neural networks. TEC-miTarget treats RNA sequences as a natural language and encodes them using a transformer encoder, a widely used encoder in natural language processing. It then combines the representations of a pair of microRNA and its candidate target site sequences into a contact map, which is a three-dimensional array similar to a multi-channel image. Therefore, the contact map's features are extracted using a four-layer convolutional neural network, enabling the prediction of interactions between microRNA and its candidate target sites. We applied a series of comparative experiments to demonstrate that TEC-miTarget significantly improves microRNA target prediction, compared with existing state-of-the-art models. Our approach is the first approach to perform comparisons with other approaches at both sequence and transcript levels. Furthermore, it is the first approach compared with both deep learning-based and seed-match-based methods. We first compared TEC-miTarget's performance with approaches at the sequence level, and our approach delivers substantial improvements in performance using the same datasets and evaluation metrics. Moreover, we utilized TEC-miTarget to predict microRNA targets in long mRNA sequences, which involves two steps: selecting candidate target site sequences and applying sequence-level predictions. We finally showed that TEC-miTarget outperforms other approaches at the transcript level, including the popular seed match methods widely used in previous years.CONCLUSIONSWe propose a novel approach for predicting microRNA targets at both sequence and transcript levels, and demonstrate that our approach outperforms other methods based on deep learning or seed match. We also provide our approach as an easy-to-use software, TEC-miTarget, at https://github.com/tingpeng17/TEC-miTarget . Our results provide new perspectives for microRNA target prediction.
Abstract Background MicroRNAs play a critical role in regulating gene expression by binding to specific target sites within gene transcripts, making the identification of microRNA targets a prominent focus of research. Conventional experimental methods for identifying microRNA targets are both time-consuming and expensive, prompting the development of computational tools for target prediction. However, the existing computational tools exhibit limited performance in meeting the demands of practical applications, highlighting the need to improve the performance of microRNA target prediction models. Results In this paper, we utilize the most popular natural language processing and computer vision technologies to propose a novel approach, called TEC-miTarget, for microRNA target prediction based on transformer encoder and convolutional neural networks. TEC-miTarget treats RNA sequences as a natural language and encodes them using a transformer encoder, a widely used encoder in natural language processing. It then combines the representations of a pair of microRNA and its candidate target site sequences into a contact map, which is a three-dimensional array similar to a multi-channel image. Therefore, the contact map's features are extracted using a four-layer convolutional neural network, enabling the prediction of interactions between microRNA and its candidate target sites. We applied a series of comparative experiments to demonstrate that TEC-miTarget significantly improves microRNA target prediction, compared with existing state-of-the-art models. Our approach is the first approach to perform comparisons with other approaches at both sequence and transcript levels. Furthermore, it is the first approach compared with both deep learning-based and seed-match-based methods. We first compared TEC-miTarget’s performance with approaches at the sequence level, and our approach delivers substantial improvements in performance using the same datasets and evaluation metrics. Moreover, we utilized TEC-miTarget to predict microRNA targets in long mRNA sequences, which involves two steps: selecting candidate target site sequences and applying sequence-level predictions. We finally showed that TEC-miTarget outperforms other approaches at the transcript level, including the popular seed match methods widely used in previous years. Conclusions We propose a novel approach for predicting microRNA targets at both sequence and transcript levels, and demonstrate that our approach outperforms other methods based on deep learning or seed match. We also provide our approach as an easy-to-use software, TEC-miTarget, at https://github.com/tingpeng17/TEC-miTarget . Our results provide new perspectives for microRNA target prediction.
Background MicroRNAs play a critical role in regulating gene expression by binding to specific target sites within gene transcripts, making the identification of microRNA targets a prominent focus of research. Conventional experimental methods for identifying microRNA targets are both time-consuming and expensive, prompting the development of computational tools for target prediction. However, the existing computational tools exhibit limited performance in meeting the demands of practical applications, highlighting the need to improve the performance of microRNA target prediction models. Results In this paper, we utilize the most popular natural language processing and computer vision technologies to propose a novel approach, called TEC-miTarget, for microRNA target prediction based on transformer encoder and convolutional neural networks. TEC-miTarget treats RNA sequences as a natural language and encodes them using a transformer encoder, a widely used encoder in natural language processing. It then combines the representations of a pair of microRNA and its candidate target site sequences into a contact map, which is a three-dimensional array similar to a multi-channel image. Therefore, the contact map's features are extracted using a four-layer convolutional neural network, enabling the prediction of interactions between microRNA and its candidate target sites. We applied a series of comparative experiments to demonstrate that TEC-miTarget significantly improves microRNA target prediction, compared with existing state-of-the-art models. Our approach is the first approach to perform comparisons with other approaches at both sequence and transcript levels. Furthermore, it is the first approach compared with both deep learning-based and seed-match-based methods. We first compared TEC-miTarget's performance with approaches at the sequence level, and our approach delivers substantial improvements in performance using the same datasets and evaluation metrics. Moreover, we utilized TEC-miTarget to predict microRNA targets in long mRNA sequences, which involves two steps: selecting candidate target site sequences and applying sequence-level predictions. We finally showed that TEC-miTarget outperforms other approaches at the transcript level, including the popular seed match methods widely used in previous years. Conclusions We propose a novel approach for predicting microRNA targets at both sequence and transcript levels, and demonstrate that our approach outperforms other methods based on deep learning or seed match. We also provide our approach as an easy-to-use software, TEC-miTarget, at Keywords: MicroRNAs, miRNA targets, Target prediction, Deep learning, Transformer encoder, Convolutional neural networks
MicroRNAs play a critical role in regulating gene expression by binding to specific target sites within gene transcripts, making the identification of microRNA targets a prominent focus of research. Conventional experimental methods for identifying microRNA targets are both time-consuming and expensive, prompting the development of computational tools for target prediction. However, the existing computational tools exhibit limited performance in meeting the demands of practical applications, highlighting the need to improve the performance of microRNA target prediction models. In this paper, we utilize the most popular natural language processing and computer vision technologies to propose a novel approach, called TEC-miTarget, for microRNA target prediction based on transformer encoder and convolutional neural networks. TEC-miTarget treats RNA sequences as a natural language and encodes them using a transformer encoder, a widely used encoder in natural language processing. It then combines the representations of a pair of microRNA and its candidate target site sequences into a contact map, which is a three-dimensional array similar to a multi-channel image. Therefore, the contact map's features are extracted using a four-layer convolutional neural network, enabling the prediction of interactions between microRNA and its candidate target sites. We applied a series of comparative experiments to demonstrate that TEC-miTarget significantly improves microRNA target prediction, compared with existing state-of-the-art models. Our approach is the first approach to perform comparisons with other approaches at both sequence and transcript levels. Furthermore, it is the first approach compared with both deep learning-based and seed-match-based methods. We first compared TEC-miTarget's performance with approaches at the sequence level, and our approach delivers substantial improvements in performance using the same datasets and evaluation metrics. Moreover, we utilized TEC-miTarget to predict microRNA targets in long mRNA sequences, which involves two steps: selecting candidate target site sequences and applying sequence-level predictions. We finally showed that TEC-miTarget outperforms other approaches at the transcript level, including the popular seed match methods widely used in previous years. We propose a novel approach for predicting microRNA targets at both sequence and transcript levels, and demonstrate that our approach outperforms other methods based on deep learning or seed match. We also provide our approach as an easy-to-use software, TEC-miTarget, at https://github.com/tingpeng17/TEC-miTarget . Our results provide new perspectives for microRNA target prediction.
ArticleNumber 159
Audience Academic
Author Wang, Yu
He, Yonghong
Yang, Tingpeng
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Cites_doi 10.1093/bioinformatics/btab733
10.1038/ng2135
10.1186/s12859-023-05564-x
10.1016/S0731-7085(99)00272-1
10.1371/journal.pcbi.1006185
10.1109/ICEngTechnol.2017.8308186
10.1016/0377-2217(80)90084-3
10.1109/78.650093
10.7554/eLife.05005
10.1186/s12859-021-04026-6
10.1109/ACCESS.2020.3034681
10.1016/j.neunet.2018.11.005
10.1145/2975167.2975212
10.1016/S0969-2126(00)00112-X
10.1093/bioinformatics/bty424
10.1016/S0092-8674(03)01018-3
10.1016/j.cell.2013.03.043
10.1093/bioinformatics/btw002
10.1007/978-1-4842-6168-2_6
10.1093/bioinformatics/bts043
10.1186/gb-2010-11-8-r90
10.1186/1752-0509-5-136
10.1007/978-3-031-20056-4_7
10.1080/20964471.2019.1657720
10.1016/j.patcog.2018.12.029
10.1016/j.cels.2021.08.010
10.1186/s13059-019-1629-z
10.1016/j.aiopen.2021.01.001
10.1164/rccm.201604-0814OC
10.4161/auto.26534
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Issue 1
Keywords Deep learning
Transformer encoder
Convolutional neural networks
MicroRNAs
miRNA targets
Target prediction
Language English
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References M Reczko (5780_CR10) 2012; 28
G Wan (5780_CR3) 2014; 10
K Eckle (5780_CR31) 2019; 110
E Westhof (5780_CR35) 2000; 8
T Gu (5780_CR17) 2021; 22
BP Lewis (5780_CR12) 2003; 115
5780_CR29
5780_CR28
W Liu (5780_CR9) 2019; 20
B Lee (5780_CR23) 2020; 8
S Sledzieski (5780_CR33) 2021; 12
X Wang (5780_CR4) 2016; 32
EA Silver (5780_CR6) 1980; 5
5780_CR21
J Song (5780_CR27) 2019; 3
V Agarwal (5780_CR11) 2015; 4
U Ruby (5780_CR34) 2020; 9
D Betel (5780_CR8) 2010; 11
5780_CR25
S Sass (5780_CR1) 2011; 5
5780_CR22
S Min (5780_CR24) 2022; 38
C-L Zhang (5780_CR30) 2019; 89
M Wen (5780_CR13) 2018; 34
A Vaswani (5780_CR26) 2017; 30
M Kertesz (5780_CR7) 2007; 39
C Barbato (5780_CR36) 2009; 8
A Pla (5780_CR15) 2018; 14
M Schuster (5780_CR19) 1997; 45
5780_CR18
A Helwak (5780_CR5) 2013; 153
Z Hong (5780_CR2) 2017; 195
5780_CR32
S Agatonovic-Kustrin (5780_CR16) 2000; 22
5780_CR14
J Przybyszewski (5780_CR20) 2023; 24
References_xml – volume: 38
  start-page: 671
  issue: 3
  year: 2022
  ident: 5780_CR24
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/btab733
  contributor:
    fullname: S Min
– volume: 39
  start-page: 1278
  issue: 10
  year: 2007
  ident: 5780_CR7
  publication-title: Nat Genet
  doi: 10.1038/ng2135
  contributor:
    fullname: M Kertesz
– volume: 24
  start-page: 436
  issue: 1
  year: 2023
  ident: 5780_CR20
  publication-title: BMC Bioinform
  doi: 10.1186/s12859-023-05564-x
  contributor:
    fullname: J Przybyszewski
– volume: 9
  start-page: 10
  year: 2020
  ident: 5780_CR34
  publication-title: Int J Adv Trends Comput Sci Eng
  contributor:
    fullname: U Ruby
– volume: 22
  start-page: 717
  issue: 5
  year: 2000
  ident: 5780_CR16
  publication-title: J Pharmaceut Biomed Anal
  doi: 10.1016/S0731-7085(99)00272-1
  contributor:
    fullname: S Agatonovic-Kustrin
– volume: 14
  start-page: e1006185
  issue: 7
  year: 2018
  ident: 5780_CR15
  publication-title: PLoS Comput Biol
  doi: 10.1371/journal.pcbi.1006185
  contributor:
    fullname: A Pla
– ident: 5780_CR18
  doi: 10.1109/ICEngTechnol.2017.8308186
– volume: 30
  start-page: 5998
  year: 2017
  ident: 5780_CR26
  publication-title: Adv Neural Inf Process Syst
  contributor:
    fullname: A Vaswani
– volume: 5
  start-page: 153
  issue: 3
  year: 1980
  ident: 5780_CR6
  publication-title: Eur J Oper Res
  doi: 10.1016/0377-2217(80)90084-3
  contributor:
    fullname: EA Silver
– volume: 8
  start-page: 2009
  year: 2009
  ident: 5780_CR36
  publication-title: BioMed Res Int
  contributor:
    fullname: C Barbato
– volume: 45
  start-page: 2673
  issue: 11
  year: 1997
  ident: 5780_CR19
  publication-title: IEEE Trans Signal Process
  doi: 10.1109/78.650093
  contributor:
    fullname: M Schuster
– volume: 4
  start-page: e05005
  year: 2015
  ident: 5780_CR11
  publication-title: Elife
  doi: 10.7554/eLife.05005
  contributor:
    fullname: V Agarwal
– volume: 22
  start-page: 1
  year: 2021
  ident: 5780_CR17
  publication-title: BMC Bioinform
  doi: 10.1186/s12859-021-04026-6
  contributor:
    fullname: T Gu
– volume: 8
  start-page: 197908
  year: 2020
  ident: 5780_CR23
  publication-title: IEEE Access
  doi: 10.1109/ACCESS.2020.3034681
  contributor:
    fullname: B Lee
– ident: 5780_CR28
– volume: 110
  start-page: 232
  year: 2019
  ident: 5780_CR31
  publication-title: Neural Netw
  doi: 10.1016/j.neunet.2018.11.005
  contributor:
    fullname: K Eckle
– ident: 5780_CR22
  doi: 10.1145/2975167.2975212
– volume: 8
  start-page: R55
  issue: 3
  year: 2000
  ident: 5780_CR35
  publication-title: Structure
  doi: 10.1016/S0969-2126(00)00112-X
  contributor:
    fullname: E Westhof
– volume: 34
  start-page: 3781
  issue: 22
  year: 2018
  ident: 5780_CR13
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/bty424
  contributor:
    fullname: M Wen
– volume: 115
  start-page: 787
  issue: 7
  year: 2003
  ident: 5780_CR12
  publication-title: Cell
  doi: 10.1016/S0092-8674(03)01018-3
  contributor:
    fullname: BP Lewis
– volume: 153
  start-page: 654
  issue: 3
  year: 2013
  ident: 5780_CR5
  publication-title: Cell
  doi: 10.1016/j.cell.2013.03.043
  contributor:
    fullname: A Helwak
– volume: 32
  start-page: 1316
  issue: 9
  year: 2016
  ident: 5780_CR4
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/btw002
  contributor:
    fullname: X Wang
– ident: 5780_CR25
  doi: 10.1007/978-1-4842-6168-2_6
– volume: 28
  start-page: 771
  issue: 6
  year: 2012
  ident: 5780_CR10
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/bts043
  contributor:
    fullname: M Reczko
– volume: 11
  start-page: 1
  year: 2010
  ident: 5780_CR8
  publication-title: Genome Biol
  doi: 10.1186/gb-2010-11-8-r90
  contributor:
    fullname: D Betel
– volume: 5
  start-page: 1
  issue: 1
  year: 2011
  ident: 5780_CR1
  publication-title: BMC Syst Biol
  doi: 10.1186/1752-0509-5-136
  contributor:
    fullname: S Sass
– ident: 5780_CR14
  doi: 10.1007/978-3-031-20056-4_7
– volume: 3
  start-page: 232
  issue: 3
  year: 2019
  ident: 5780_CR27
  publication-title: Big Earth Data
  doi: 10.1080/20964471.2019.1657720
  contributor:
    fullname: J Song
– volume: 89
  start-page: 12
  year: 2019
  ident: 5780_CR30
  publication-title: Pattern Recogn
  doi: 10.1016/j.patcog.2018.12.029
  contributor:
    fullname: C-L Zhang
– volume: 12
  start-page: 969
  issue: 10
  year: 2021
  ident: 5780_CR33
  publication-title: Cell Syst
  doi: 10.1016/j.cels.2021.08.010
  contributor:
    fullname: S Sledzieski
– volume: 20
  start-page: 1
  year: 2019
  ident: 5780_CR9
  publication-title: Genome Biol
  doi: 10.1186/s13059-019-1629-z
  contributor:
    fullname: W Liu
– ident: 5780_CR21
  doi: 10.1016/j.aiopen.2021.01.001
– ident: 5780_CR29
– volume: 195
  start-page: 515
  issue: 4
  year: 2017
  ident: 5780_CR2
  publication-title: Am J Respir Crit Care Med
  doi: 10.1164/rccm.201604-0814OC
  contributor:
    fullname: Z Hong
– ident: 5780_CR32
– volume: 10
  start-page: 70
  issue: 1
  year: 2014
  ident: 5780_CR3
  publication-title: Autophagy
  doi: 10.4161/auto.26534
  contributor:
    fullname: G Wan
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Snippet MicroRNAs play a critical role in regulating gene expression by binding to specific target sites within gene transcripts, making the identification of microRNA...
Abstract Background MicroRNAs play a critical role in regulating gene expression by binding to specific target sites within gene transcripts, making the...
Background MicroRNAs play a critical role in regulating gene expression by binding to specific target sites within gene transcripts, making the identification...
BackgroundMicroRNAs play a critical role in regulating gene expression by binding to specific target sites within gene transcripts, making the identification...
BACKGROUNDMicroRNAs play a critical role in regulating gene expression by binding to specific target sites within gene transcripts, making the identification...
Abstract Background MicroRNAs play a critical role in regulating gene expression by binding to specific target sites within gene transcripts, making the...
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StartPage 159
SubjectTerms Analysis
Artificial neural networks
Coders
Computational linguistics
Computer applications
Computer vision
Convolutional neural networks
Datasets
Deep Learning
Experimental methods
Gene expression
Gene sequencing
Genes
Language
Language processing
Machine learning
Machine vision
Messenger RNA
MicroRNA
MicroRNAs
MicroRNAs - genetics
MicroRNAs - metabolism
miRNA
miRNA targets
Natural language
Natural language interfaces
Natural language processing
Neural networks
Neural Networks, Computer
Nucleotides
Performance enhancement
Prediction models
Properties
Ribonucleic acid
RNA
RNA, Messenger - genetics
Software
Target prediction
Transformer encoder
Transformers
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Title TEC-miTarget: enhancing microRNA target prediction based on deep learning of ribonucleic acid sequences
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