Region-Based Image Clustering and Retrieval Using Multiple Instance Learning

Author(s):  
Chengcui Zhang ◽  
Xin Chen
2021 ◽  
Author(s):  
Marc-Henri Bleu-Laine ◽  
Tejas G. Puranik ◽  
Dimitri N. Mavris ◽  
Bryan Matthews

Author(s):  
Xiaochuan Tang ◽  
Mingzhe Liu ◽  
Hao Zhong ◽  
Yuanzhen Ju ◽  
Weile Li ◽  
...  

Landslide recognition is widely used in natural disaster risk management. Traditional landslide recognition is mainly conducted by geologists, which is accurate but inefficient. This article introduces multiple instance learning (MIL) to perform automatic landslide recognition. An end-to-end deep convolutional neural network is proposed, referred to as Multiple Instance Learning–based Landslide classification (MILL). First, MILL uses a large-scale remote sensing image classification dataset to build pre-train networks for landslide feature extraction. Second, MILL extracts instances and assign instance labels without pixel-level annotations. Third, MILL uses a new channel attention–based MIL pooling function to map instance-level labels to bag-level label. We apply MIL to detect landslides in a loess area. Experimental results demonstrate that MILL is effective in identifying landslides in remote sensing images.


2021 ◽  
Vol 38 ◽  
pp. 301171
Author(s):  
Rahimeh Rouhi ◽  
Flavio Bertini ◽  
Danilo Montesi

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Marleen M. Nieboer ◽  
Luan Nguyen ◽  
Jeroen de Ridder

AbstractOver the past years, large consortia have been established to fuel the sequencing of whole genomes of many cancer patients. Despite the increased abundance in tools to study the impact of SNVs, non-coding SVs have been largely ignored in these data. Here, we introduce svMIL2, an improved version of our Multiple Instance Learning-based method to study the effect of somatic non-coding SVs disrupting boundaries of TADs and CTCF loops in 1646 cancer genomes. We demonstrate that svMIL2 predicts pathogenic non-coding SVs with an average AUC of 0.86 across 12 cancer types, and identifies non-coding SVs affecting well-known driver genes. The disruption of active (super) enhancers in open chromatin regions appears to be a common mechanism by which non-coding SVs exert their pathogenicity. Finally, our results reveal that the contribution of pathogenic non-coding SVs as opposed to driver SNVs may highly vary between cancers, with notably high numbers of genes being disrupted by pathogenic non-coding SVs in ovarian and pancreatic cancer. Taken together, our machine learning method offers a potent way to prioritize putatively pathogenic non-coding SVs and leverage non-coding SVs to identify driver genes. Moreover, our analysis of 1646 cancer genomes demonstrates the importance of including non-coding SVs in cancer diagnostics.


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