scholarly journals iEnhancer-GAN: A Deep Learning Framework in Combination with Word Embedding and Sequence Generative Adversarial Net to Identify Enhancers and Their Strength

2021 ◽  
Vol 22 (7) ◽  
pp. 3589
Author(s):  
Runtao Yang ◽  
Feng Wu ◽  
Chengjin Zhang ◽  
Lina Zhang
Keyword(s):  
Deep Learning ◽  
Gene Transcription ◽  
Dna Sequences ◽  
Word Segmentation ◽  
Word Embedding ◽  
Training Dataset ◽  
Prediction Ability ◽  
Learning Framework ◽  
Segmentation Methods ◽  
Human Pathology

As critical components of DNA, enhancers can efficiently and specifically manipulate the spatial and temporal regulation of gene transcription. Malfunction or dysregulation of enhancers is implicated in a slew of human pathology. Therefore, identifying enhancers and their strength may provide insights into the molecular mechanisms of gene transcription and facilitate the discovery of candidate drug targets. In this paper, a new enhancer and its strength predictor, iEnhancer-GAN, is proposed based on a deep learning framework in combination with the word embedding and sequence generative adversarial net (Seq-GAN). Considering the relatively small training dataset, the Seq-GAN is designed to generate artificial sequences. Given that each functional element in DNA sequences is analogous to a “word” in linguistics, the word segmentation methods are proposed to divide DNA sequences into “words”, and the skip-gram model is employed to transform the “words” into digital vectors. In view of the powerful ability to extract high-level abstraction features, a convolutional neural network (CNN) architecture is constructed to perform the identification tasks, and the word vectors of DNA sequences are vertically concatenated to form the embedding matrices as the input of the CNN. Experimental results demonstrate the effectiveness of the Seq-GAN to expand the training dataset, the possibility of applying word segmentation methods to extract “words” from DNA sequences, the feasibility of implementing the skip-gram model to encode DNA sequences, and the powerful prediction ability of the CNN. Compared with other state-of-the-art methods on the training dataset and independent test dataset, the proposed method achieves a significantly improved overall performance. It is anticipated that the proposed method has a certain promotion effect on enhancer related fields.

scholarly journals ViraMiner: Deep Learning on Raw DNA Sequences for Identifying Viral Genomes in Human Samples

2019 ◽  
Author(s):  
Ardi Tampuu ◽  
Zurab Bzhalava ◽  
Joakim Dillner ◽  
Raul Vicente
Keyword(s):  
Machine Learning ◽  
Deep Learning ◽  
Dna Sequences ◽  
Recommendation System ◽  
Clinical Importance ◽  
Training Dataset ◽  
Viral Genomes ◽  
Human Samples ◽  
Types Of Information ◽  
Improved Accuracy

ABSTRACTDespite its clinical importance, detection of highly divergent or yet unknown viruses is a major challenge. When human samples are sequenced, conventional alignments classify many assembled contigs as “unknown” since many of the sequences are not similar to known genomes. In this work, we developed ViraMiner, a deep learning-based method to identify viruses in various human biospecimens. ViraMiner contains two branches of Convolutional Neural Networks designed to detect both patterns and pattern-frequencies on raw metagenomics contigs. The training dataset included sequences obtained from 19 metagenomic experiments which were analyzed and labeled by BLAST. The model achieves significantly improved accuracy compared to other machine learning methods for viral genome classification. Using 300 bp contigs ViraMiner achieves 0.923 area under the ROC curve. To our knowledge, this is the first machine learning methodology that can detect the presence of viral sequences among raw metagenomic contigs from diverse human samples. We suggest that the proposed model captures different types of information of genome composition, and can be used as a recommendation system to further investigate sequences labeled as “unknown” by conventional alignment methods. Exploring these highly-divergent viruses, in turn, can enhance our knowledge of infectious causes of diseases.

scholarly journals A deep learning framework combined with word embedding to identify DNA replication origins

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Feng Wu ◽  
Runtao Yang ◽  
Chengjin Zhang ◽  
Lina Zhang
Keyword(s):  
Deep Learning ◽  
Dna Replication ◽  
Machine Learning Algorithms ◽  
Word Embedding ◽  
Correct Identification ◽  
Replication Origins ◽  
Gene Sequences ◽  
Replication Process ◽  
Similarity Reduction ◽  
Learning Framework

AbstractThe DNA replication influences the inheritance of genetic information in the DNA life cycle. As the distribution of replication origins (ORIs) is the major determinant to precisely regulate the replication process, the correct identification of ORIs is significant in giving an insightful understanding of DNA replication mechanisms and the regulatory mechanisms of genetic expressions. For eukaryotes in particular, multiple ORIs exist in each of their gene sequences to complete the replication in a reasonable period of time. To simplify the identification process of eukaryote’s ORIs, most of existing methods are developed by traditional machine learning algorithms, and target to the gene sequences with a fixed length. Consequently, the identification results are not satisfying, i.e. there is still great room for improvement. To break through the limitations in previous studies, this paper develops sequence segmentation methods, and employs the word embedding technique, ‘Word2vec’, to convert gene sequences into word vectors, thereby grasping the inner correlations of gene sequences with different lengths. Then, a deep learning framework to perform the ORI identification task is constructed by a convolutional neural network with an embedding layer. On the basis of the analysis of similarity reduction dimensionality diagram, Word2vec can effectively transform the inner relationship among words into numerical feature. For four species in this study, the best models are obtained with the overall accuracy of 0.975, 0.765, 0.885, 0.967, the Matthew’s correlation coefficient of 0.940, 0.530, 0.771, 0.934, and the AUC of 0.975, 0.800, 0.888, 0.981, which indicate that the proposed predictor has a stable ability and provide a high confidence coefficient to classify both of ORIs and non-ORIs. Compared with state-of-the-art methods, the proposed predictor can achieve ORI identification with significant improvement. It is therefore reasonable to anticipate that the proposed method will make a useful high throughput tool for genome analysis.

scholarly journals Efficient Stain-Aware Nuclei Segmentation Deep Learning Framework for Multi-Center Histopathological Images

Electronics ◽  
2021 ◽  
Vol 10 (8) ◽  
pp. 954
Author(s):  
Loay Hassan ◽  
Mohamed Abdel-Nasser ◽  
Adel Saleh ◽  
Osama A. Omer ◽  
Domenec Puig
Keyword(s):  
Deep Learning ◽  
Choquet Integral ◽  
Adjacent Cell ◽  
Cell Nuclei ◽  
Nuclei Segmentation ◽  
Learning Framework ◽  
Segmentation Methods ◽  
Histopathological Images ◽  
The Individual ◽  
Whole Slide Images

Existing nuclei segmentation methods have obtained limited results with multi-center and multi-organ whole-slide images (WSIs) due to the use of different stains, scanners, overlapping, clumped nuclei, and the ambiguous boundary between adjacent cell nuclei. In an attempt to address these problems, we propose an efficient stain-aware nuclei segmentation method based on deep learning for multi-center WSIs. Unlike all related works that exploit a single-stain template from the dataset to normalize WSIs, we propose an efficient algorithm to select a set of stain templates based on stain clustering. Individual deep learning models are trained based on each stain template, and then, an aggregation function based on the Choquet integral is employed to combine the segmentation masks of the individual models. With a challenging multi-center multi-organ WSIs dataset, the experimental results demonstrate that the proposed method outperforms the state-of-art nuclei segmentation methods with aggregated Jaccard index (AJI) and F1-scores of 73.23% and 89.32%, respectively, while achieving a lower number of parameters.

scholarly journals DeepHINT: Understanding HIV-1 integration via deep learning with attention

2018 ◽  
Author(s):  
Hailin Hu ◽  
An Xiao ◽  
Sai Zhang ◽  
Yangyang Li ◽  
Xuanling Shi ◽  
...  
Keyword(s):  
Deep Learning ◽  
Dna Sequences ◽  
Mechanistic Study ◽  
Sequence Information ◽  
Genomic Context ◽  
Learning Framework ◽  
Integration Sites ◽  
Hiv Integration ◽  
Hiv 1 ◽  
Selection Of

AbstractMotivationHuman immunodeficiency virus type 1 (HIV-1) genome integration is closely related to clinical latency and viral rebound. In addition to human DNA sequences that directly interact with the integration machinery, the selection of HIV integration sites has also been shown to depend on the heterogeneous genomic context around a large region, which greatly hinders the prediction and mechanistic studies of HIV integration.ResultsWe have developed an attention-based deep learning framework, named DeepHINT, to simultaneously provide accurate prediction of HIV integration sites and mechanistic explanations of the detected sites. Extensive tests on a high-density HIV integration site dataset showed that DeepHINT can outperform conventional modeling strategies by automatically learning the genomic context of HIV integration solely from primary DNA sequence information. Systematic analyses on diverse known factors of HIV integration further validated the biological relevance of the prediction result. More importantly, in-depth analyses of the attention values output by DeepHINT revealed intriguing mechanistic implications in the selection of HIV integration sites, including potential roles of several basic helix-loop-helix (bHLH) transcription factors and zinc-finger proteins. These results established DeepHINT as an effective and explainable deep learning framework for the prediction and mechanistic study of HIV integration.AvailabilityDeepHINT is available as an open-source software and can be downloaded fromhttps://github.com/nonnerdling/[email protected]@tsinghua.edu.cn

scholarly journals Degradation-Aware Deep Learning Framework for Sparse-View CT Reconstruction

Tomography ◽  
2021 ◽  
Vol 7 (4) ◽  
pp. 932-949
Author(s):  
Chang Sun ◽  
Yitong Liu ◽  
Hongwen Yang
Keyword(s):  
Deep Learning ◽  
Structural Similarity ◽  
Frequency Component ◽  
Ct Images ◽  
Training Dataset ◽  
Ct Reconstruction ◽  
Reconstruction Algorithms ◽  
Image Domain ◽  
Learning Framework ◽  
Reconstruction Methods

Sparse-view CT reconstruction is a fundamental task in computed tomography to overcome undesired artifacts and recover the details of textual structure in degraded CT images. Recently, many deep learning-based networks have achieved desirable performances compared to iterative reconstruction algorithms. However, the performance of these methods may severely deteriorate when the degradation strength of the test image is not consistent with that of the training dataset. In addition, these methods do not pay enough attention to the characteristics of different degradation levels, so solely extending the training dataset with multiple degraded images is also not effective. Although training plentiful models in terms of each degradation level can mitigate this problem, extensive parameter storage is involved. Accordingly, in this paper, we focused on sparse-view CT reconstruction for multiple degradation levels. We propose a single degradation-aware deep learning framework to predict clear CT images by understanding the disparity of degradation in both the frequency domain and image domain. The dual-domain procedure can perform particular operations at different degradation levels in frequency component recovery and spatial details reconstruction. The peak signal-to-noise ratio (PSNR), structural similarity (SSIM) and visual results demonstrate that our method outperformed the classical deep learning-based reconstruction methods in terms of effectiveness and scalability.

A Deep Learning Framework for Prediction of Retinal Disorders

2020 ◽  
Author(s):  
Raniyaharini R ◽  
Madhumitha K ◽  
Mishaa S ◽  
Virajaravi R
Keyword(s):  
Deep Learning ◽  
Learning Framework ◽  
Retinal Disorders

Sequence-Based Deep Learning Frameworks on Enhancer-Promoter Interactions Prediction

2020 ◽  
Vol 26 ◽  
Author(s):  
Xiaoping Min ◽  
Fengqing Lu ◽  
Chunyan Li
Keyword(s):  
Gene Expression ◽  
Deep Learning ◽  
Dna Sequences ◽  
Experimental Methods ◽  
Learning Methods ◽  
Comprehensive Review ◽  
Genomic Features ◽  
Disease Mechanisms ◽  
Evaluation Strategies ◽  
Learning Frameworks

: Enhancer-promoter interactions (EPIs) in the human genome are of great significance to transcriptional regulation which tightly controls gene expression. Identification of EPIs can help us better deciphering gene regulation and understanding disease mechanisms. However, experimental methods to identify EPIs are constrained by the fund, time and manpower while computational methods using DNA sequences and genomic features are viable alternatives. Deep learning methods have shown promising prospects in classification and efforts that have been utilized to identify EPIs. In this survey, we specifically focus on sequence-based deep learning methods and conduct a comprehensive review of the literatures of them. We first briefly introduce existing sequence-based frameworks on EPIs prediction and their technique details. After that, we elaborate on the dataset, pre-processing means and evaluation strategies. Finally, we discuss the challenges these methods are confronted with and suggest several future opportunities.

COVID-19 pneumonia diagnosis using a simple 2D deep learning framework with a single chest CT image (Preprint)

2020 ◽  
Author(s):  
Jinseok Lee
Keyword(s):  
Deep Learning ◽  
Diagnostic Performance ◽  
Ct Images ◽  
Chest Ct ◽  
University Hospital ◽  
Detection Accuracy ◽  
Ct Image ◽  
Test Dataset ◽  
Learning Framework ◽  
Testing Dataset

BACKGROUND The coronavirus disease (COVID-19) has explosively spread worldwide since the beginning of 2020. According to a multinational consensus statement from the Fleischner Society, computed tomography (CT) can be used as a relevant screening tool owing to its higher sensitivity for detecting early pneumonic changes. However, physicians are extremely busy fighting COVID-19 in this era of worldwide crisis. Thus, it is crucial to accelerate the development of an artificial intelligence (AI) diagnostic tool to support physicians. OBJECTIVE We aimed to quickly develop an AI technique to diagnose COVID-19 pneumonia and differentiate it from non-COVID pneumonia and non-pneumonia diseases on CT. METHODS A simple 2D deep learning framework, named fast-track COVID-19 classification network (FCONet), was developed to diagnose COVID-19 pneumonia based on a single chest CT image. FCONet was developed by transfer learning, using one of the four state-of-art pre-trained deep learning models (VGG16, ResNet50, InceptionV3, or Xception) as a backbone. For training and testing of FCONet, we collected 3,993 chest CT images of patients with COVID-19 pneumonia, other pneumonia, and non-pneumonia diseases from Wonkwang University Hospital, Chonnam National University Hospital, and the Italian Society of Medical and Interventional Radiology public database. These CT images were split into a training and a testing set at a ratio of 8:2. For the test dataset, the diagnostic performance to diagnose COVID-19 pneumonia was compared among the four pre-trained FCONet models. In addition, we tested the FCONet models on an additional external testing dataset extracted from the embedded low-quality chest CT images of COVID-19 pneumonia in recently published papers. RESULTS Of the four pre-trained models of FCONet, the ResNet50 showed excellent diagnostic performance (sensitivity 99.58%, specificity 100%, and accuracy 99.87%) and outperformed the other three pre-trained models in testing dataset. In additional external test dataset using low-quality CT images, the detection accuracy of the ResNet50 model was the highest (96.97%), followed by Xception, InceptionV3, and VGG16 (90.71%, 89.38%, and 87.12%, respectively). CONCLUSIONS The FCONet, a simple 2D deep learning framework based on a single chest CT image, provides excellent diagnostic performance in detecting COVID-19 pneumonia. Based on our testing dataset, the ResNet50-based FCONet might be the best model, as it outperformed other FCONet models based on VGG16, Xception, and InceptionV3.

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