scholarly journals Prototype vector machine for large scale semi-supervised learning

Author(s):  
Kai Zhang ◽  
James T. Kwok ◽  
Bahram Parvin
Technologies ◽  
2020 ◽  
Vol 9 (1) ◽  
pp. 2
Author(s):  
Ashish Jaiswal ◽  
Ashwin Ramesh Babu ◽  
Mohammad Zaki Zadeh ◽  
Debapriya Banerjee ◽  
Fillia Makedon

Self-supervised learning has gained popularity because of its ability to avoid the cost of annotating large-scale datasets. It is capable of adopting self-defined pseudolabels as supervision and use the learned representations for several downstream tasks. Specifically, contrastive learning has recently become a dominant component in self-supervised learning for computer vision, natural language processing (NLP), and other domains. It aims at embedding augmented versions of the same sample close to each other while trying to push away embeddings from different samples. This paper provides an extensive review of self-supervised methods that follow the contrastive approach. The work explains commonly used pretext tasks in a contrastive learning setup, followed by different architectures that have been proposed so far. Next, we present a performance comparison of different methods for multiple downstream tasks such as image classification, object detection, and action recognition. Finally, we conclude with the limitations of the current methods and the need for further techniques and future directions to make meaningful progress.


2020 ◽  
Vol 34 (05) ◽  
pp. 9193-9200
Author(s):  
Shaolei Wang ◽  
Wangxiang Che ◽  
Qi Liu ◽  
Pengda Qin ◽  
Ting Liu ◽  
...  

Most existing approaches to disfluency detection heavily rely on human-annotated data, which is expensive to obtain in practice. To tackle the training data bottleneck, we investigate methods for combining multiple self-supervised tasks-i.e., supervised tasks where data can be collected without manual labeling. First, we construct large-scale pseudo training data by randomly adding or deleting words from unlabeled news data, and propose two self-supervised pre-training tasks: (i) tagging task to detect the added noisy words. (ii) sentence classification to distinguish original sentences from grammatically-incorrect sentences. We then combine these two tasks to jointly train a network. The pre-trained network is then fine-tuned using human-annotated disfluency detection training data. Experimental results on the commonly used English Switchboard test set show that our approach can achieve competitive performance compared to the previous systems (trained using the full dataset) by using less than 1% (1000 sentences) of the training data. Our method trained on the full dataset significantly outperforms previous methods, reducing the error by 21% on English Switchboard.


2019 ◽  
Author(s):  
Robert Krueger ◽  
Johanna Beyer ◽  
Won-Dong Jang ◽  
Nam Wook Kim ◽  
Artem Sokolov ◽  
...  

AbstractFacetto is a scalable visual analytics application that is used to discover single-cell phenotypes in high-dimensional multi-channel microscopy images of human tumors and tissues. Such images represent the cutting edge of digital histology and promise to revolutionize how diseases such as cancer are studied, diagnosed, and treated. Highly multiplexed tissue images are complex, comprising 109or more pixels, 60-plus channels, and millions of individual cells. This makes manual analysis challenging and error-prone. Existing automated approaches are also inadequate, in large part, because they are unable to effectively exploit the deep knowledge of human tissue biology available to anatomic pathologists. To overcome these challenges, Facetto enables a semi-automated analysis of cell types and states. It integrates unsupervised and supervised learning into the image and feature exploration process and offers tools for analytical provenance. Experts can cluster the data to discover new types of cancer and immune cells and use clustering results to train a convolutional neural network that classifies new cells accordingly. Likewise, the output of classifiers can be clustered to discover aggregate patterns and phenotype subsets. We also introduce a new hierarchical approach to keep track of analysis steps and data subsets created by users; this assists in the identification of cell types. Users can build phenotype trees and interact with the resulting hierarchical structures of both high-dimensional feature and image spaces. We report on use-cases in which domain scientists explore various large-scale fluorescence imaging datasets. We demonstrate how Facetto assists users in steering the clustering and classification process, inspecting analysis results, and gaining new scientific insights into cancer biology.


Author(s):  
Shaolei Wang ◽  
Zhongyuan Wang ◽  
Wanxiang Che ◽  
Sendong Zhao ◽  
Ting Liu

Spoken language is fundamentally different from the written language in that it contains frequent disfluencies or parts of an utterance that are corrected by the speaker. Disfluency detection (removing these disfluencies) is desirable to clean the input for use in downstream NLP tasks. Most existing approaches to disfluency detection heavily rely on human-annotated data, which is scarce and expensive to obtain in practice. To tackle the training data bottleneck, in this work, we investigate methods for combining self-supervised learning and active learning for disfluency detection. First, we construct large-scale pseudo training data by randomly adding or deleting words from unlabeled data and propose two self-supervised pre-training tasks: (i) a tagging task to detect the added noisy words and (ii) sentence classification to distinguish original sentences from grammatically incorrect sentences. We then combine these two tasks to jointly pre-train a neural network. The pre-trained neural network is then fine-tuned using human-annotated disfluency detection training data. The self-supervised learning method can capture task-special knowledge for disfluency detection and achieve better performance when fine-tuning on a small annotated dataset compared to other supervised methods. However, limited in that the pseudo training data are generated based on simple heuristics and cannot fully cover all the disfluency patterns, there is still a performance gap compared to the supervised models trained on the full training dataset. We further explore how to bridge the performance gap by integrating active learning during the fine-tuning process. Active learning strives to reduce annotation costs by choosing the most critical examples to label and can address the weakness of self-supervised learning with a small annotated dataset. We show that by combining self-supervised learning with active learning, our model is able to match state-of-the-art performance with just about 10% of the original training data on both the commonly used English Switchboard test set and a set of in-house annotated Chinese data.


Symmetry ◽  
2019 ◽  
Vol 11 (2) ◽  
pp. 133 ◽  
Author(s):  
Yang Li ◽  
Ying Lv ◽  
Suge Wang ◽  
Jiye Liang ◽  
Juanzi Li ◽  
...  

A large-scale and high-quality training dataset is an important guarantee to learn an ideal classifier for text sentiment classification. However, manually constructing such a training dataset with sentiment labels is a labor-intensive and time-consuming task. Therefore, based on the idea of effectively utilizing unlabeled samples, a synthetical framework that covers the whole process of semi-supervised learning from seed selection, iterative modification of the training text set, to the co-training strategy of the classifier is proposed in this paper for text sentiment classification. To provide an important basis for selecting the seed texts and modifying the training text set, three kinds of measures—the cluster similarity degree of an unlabeled text, the cluster uncertainty degree of a pseudo-label text to a learner, and the reliability degree of a pseudo-label text to a learner—are defined. With these measures, a seed selection method based on Random Swap clustering, a hybrid modification method of the training text set based on active learning and self-learning, and an alternately co-training strategy of the ensemble classifier of the Maximum Entropy and Support Vector Machine are proposed and combined into our framework. The experimental results on three Chinese datasets (COAE2014, COAE2015, and a Hotel review, respectively) and five English datasets (Books, DVD, Electronics, Kitchen, and MR, respectively) in the real world verify the effectiveness of the proposed framework.


2019 ◽  
Author(s):  
Dimitrios Vitsios ◽  
Slavé Petrovski

AbstractAccess to large-scale genomics datasets has increased the utility of hypothesis-free genome-wide analyses that result in candidate lists of genes. Often these analyses highlight several gene signals that might contribute to pathogenesis but are insufficiently powered to reach experiment-wide significance. This often triggers a process of laborious evaluation of highly-ranked genes through manual inspection of various public knowledge resources to triage those considered sufficiently interesting for deeper investigation. Here, we introduce a novel multi-dimensional, multi-step machine learning framework to objectively and more holistically assess biological relevance of genes to disease studies, by relying on a plethora of gene-associated annotations. We developed mantis-ml to serve as an automated machine learning (AutoML) framework, following a stochastic semi-supervised learning approach to rank known and novel disease-associated genes through iterative training and prediction sessions of random balanced datasets across the protein-coding exome (n=18,626 genes). We applied this framework on a range of disease-specific areas and as a generic disease likelihood estimator, achieving an average Area Under Curve (AUC) prediction performance of 0.85. Critically, to demonstrate applied utility on exome-wide association studies, we overlapped mantis-ml disease-specific predictions with data from published cohort-level association studies. We retrieved statistically significant enrichment of high mantis-ml predictions among the top-ranked genes from hypothesis-free cohort-level statistics (p<0.05), suggesting the capture of true prioritisation signals. We believe that mantis-ml is a novel easy-to-use tool to support objectively triaging gene discovery and overall enhancing our understanding of complex genotype-phenotype associations.


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