scholarly journals Basset: Learning the regulatory code of the accessible genome with deep convolutional neural networks

2015 ◽  
Author(s):  
David R. Kelley ◽  
Jasper Snoek ◽  
John Rinn

AbstractThe complex language of eukaryotic gene expression remains incompletely understood. Despite the importance suggested by many noncoding variants statistically associated with human disease, nearly all such variants have unknown mechanism. Here, we address this challenge using an approach based on a recent machine learning advance—deep convolutional neural networks (CNNs). We introduce an open source package Basset (https://github.com/davek44/Basset) to apply CNNs to learn the functional activity of DNA sequences from genomics data. We trained Basset on a compendium of accessible genomic sites mapped in 164 cell types by DNaseI-seq and demonstrate far greater predictive accuracy than previous methods. Basset predictions for the change in accessibility between variant alleles were far greater for GWAS SNPs that are likely to be causal relative to nearby SNPs in linkage disequilibrium with them. With Basset, a researcher can perform a single sequencing assay in their cell type of interest and simultaneously learn that cell’s chromatin accessibility code and annotate every mutation in the genome with its influence on present accessibility and latent potential for accessibility. Thus, Basset offers a powerful computational approach to annotate and interpret the noncoding genome.

2021 ◽  
pp. 1-10
Author(s):  
Halime Ergun

Fiber and vessel structures located in the cross-section are anatomical features that play an important role in identifying tree species. In order to determine the microscopic anatomical structure of these cell types, each cell must be accurately segmented. In this study, a segmentation method is proposed for wood cell images based on deep convolutional neural networks. The network, which was developed by combining two-stage CNN structures, was trained using the Adam optimization algorithm. For evaluation, the method was compared with SegNet and U-Net architectures, trained with the same dataset. The losses in these models trained were compared using IoU (Intersection over Union), accuracy, and BF-score measurements on the test data. The automatic identification of the cells in the wood images obtained using a microscope will provide a fast, inexpensive, and reliable tool for those working in this field.


2019 ◽  
Vol 24 (4) ◽  
pp. 466-475 ◽  
Author(s):  
Alexander Kensert ◽  
Philip J. Harrison ◽  
Ola Spjuth

The quantification and identification of cellular phenotypes from high-content microscopy images has proven to be very useful for understanding biological activity in response to different drug treatments. The traditional approach has been to use classical image analysis to quantify changes in cell morphology, which requires several nontrivial and independent analysis steps. Recently, convolutional neural networks have emerged as a compelling alternative, offering good predictive performance and the possibility to replace traditional workflows with a single network architecture. In this study, we applied the pretrained deep convolutional neural networks ResNet50, InceptionV3, and InceptionResnetV2 to predict cell mechanisms of action in response to chemical perturbations for two cell profiling datasets from the Broad Bioimage Benchmark Collection. These networks were pretrained on ImageNet, enabling much quicker model training. We obtain higher predictive accuracy than previously reported, between 95% and 97%. The ability to quickly and accurately distinguish between different cell morphologies from a scarce amount of labeled data illustrates the combined benefit of transfer learning and deep convolutional neural networks for interrogating cell-based images.


2018 ◽  
Author(s):  
Alexander Kensert ◽  
Philip J Harrison ◽  
Ola Spjuth

AbstractQuantification and identification of cellular phenotypes from high content microscopy images have proven to be very useful for understanding biological activity in response to different drug treatments. The traditional approach has been to use classical image analysis to quantify changes in cell morphology, which requires several non-trivial and independent analysis steps. Recently convolutional neural networks have emerged as a compelling alternative, offering good predictive performance and the possibility to replace traditional workflows with a single network architecture. In this study we applied the pre-trained deep convolutional neural networks ResNet50, InceptionV3 and InceptionResnetV2 to predict cell mechanisms of action in response to chemical perturbations for two cell profiling datasets from the Broad Bioimage Benchmark Collection. These networks were pre-trained on ImageNet enabling much quicker model training. We obtain higher predictive accuracy than previously reported, between 95 and 97% based on “leave-one-compound-out” cross-validation. The ability to quickly and accurately distinguish between different cell morphologies from a scarce amount of labelled data illustrates the combined benefit of transfer learning and deep convolutional neural networks for interrogating cell-based images.


2020 ◽  
Vol 2020 (10) ◽  
pp. 28-1-28-7 ◽  
Author(s):  
Kazuki Endo ◽  
Masayuki Tanaka ◽  
Masatoshi Okutomi

Classification of degraded images is very important in practice because images are usually degraded by compression, noise, blurring, etc. Nevertheless, most of the research in image classification only focuses on clean images without any degradation. Some papers have already proposed deep convolutional neural networks composed of an image restoration network and a classification network to classify degraded images. This paper proposes an alternative approach in which we use a degraded image and an additional degradation parameter for classification. The proposed classification network has two inputs which are the degraded image and the degradation parameter. The estimation network of degradation parameters is also incorporated if degradation parameters of degraded images are unknown. The experimental results showed that the proposed method outperforms a straightforward approach where the classification network is trained with degraded images only.


2019 ◽  
Vol 277 ◽  
pp. 02024 ◽  
Author(s):  
Lincan Li ◽  
Tong Jia ◽  
Tianqi Meng ◽  
Yizhe Liu

In this paper, an accurate two-stage deep learning method is proposed to detect vulnerable plaques in ultrasonic images of cardiovascular. Firstly, a Fully Convonutional Neural Network (FCN) named U-Net is used to segment the original Intravascular Optical Coherence Tomography (IVOCT) cardiovascular images. We experiment on different threshold values to find the best threshold for removing noise and background in the original images. Secondly, a modified Faster RCNN is adopted to do precise detection. The modified Faster R-CNN utilize six-scale anchors (122,162,322,642,1282,2562) instead of the conventional one scale or three scale approaches. First, we present three problems in cardiovascular vulnerable plaque diagnosis, then we demonstrate how our method solve these problems. The proposed method in this paper apply deep convolutional neural networks to the whole diagnostic procedure. Test results show the Recall rate, Precision rate, IoU (Intersection-over-Union) rate and Total score are 0.94, 0.885, 0.913 and 0.913 respectively, higher than the 1st team of CCCV2017 Cardiovascular OCT Vulnerable Plaque Detection Challenge. AP of the designed Faster RCNN is 83.4%, higher than conventional approaches which use one-scale or three-scale anchors. These results demonstrate the superior performance of our proposed method and the power of deep learning approaches in diagnose cardiovascular vulnerable plaques.


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