Fused Text Segmentation Networks for Multi-oriented Scene Text Detection

In this paper, we introduce a novel end-end framework for multi-oriented scene text detection from an instance-aware semantic segmentation perspective. We present Fused Text Segmentation Networks, which combine multi-level features during the feature extracting as text instance may rely on finer feature expression compared to general objects. It detects and segments the text instance jointly and simultaneously, leveraging merits from both semantic segmentation task and region proposal based object detection task. Not involving any extra pipelines, our approach surpasses the current state of the art on multi-oriented scene text detection benchmarks: ICDAR2015 Incidental Scene Text and MSRA-TD500 reaching Hmean 84.1% and 82.0% respectively. Morever, we report a baseline on total-text containing curved text which suggests effectiveness of the proposed approach.Comment: Accepted by ICPR201

FSS-1000: A 1000-Class Dataset for Few-Shot Segmentation

Over the past few years, we have witnessed the success of deep learning in image recognition thanks to the availability of large-scale human-annotated datasets such as PASCAL VOC, ImageNet, and COCO. Although these datasets have covered a wide range of object categories, there are still a significant number of objects that are not included. Can we perform the same task without a lot of human annotations? In this paper, we are interested in few-shot object segmentation where the number of annotated training examples are limited to 5 only. To evaluate and validate the performance of our approach, we have built a few-shot segmentation dataset, FSS-1000, which consists of 1000 object classes with pixelwise annotation of ground-truth segmentation. Unique in FSS-1000, our dataset contains significant number of objects that have never been seen or annotated in previous datasets, such as tiny daily objects, merchandise, cartoon characters, logos, etc. We build our baseline model using standard backbone networks such as VGG-16, ResNet-101, and Inception. To our surprise, we found that training our model from scratch using FSS-1000 achieves comparable and even better results than training with weights pre-trained by ImageNet which is more than 100 times larger than FSS-1000. Both our approach and dataset are simple, effective, and easily extensible to learn segmentation of new object classes given very few annotated training examples. Dataset is available at https://github.com/HKUSTCV/FSS-1000

CDC: Convolutional-De-Convolutional Networks for Precise Temporal Action Localization in Untrimmed Videos

Temporal action localization is an important yet challenging problem. Given a long, untrimmed video consisting of multiple action instances and complex background contents, we need not only to recognize their action categories, but also to localize the start time and end time of each instance. Many state-of-the-art systems use segment-level classifiers to select and rank proposal segments of pre-determined boundaries. However, a desirable model should move beyond segment-level and make dense predictions at a fine granularity in time to determine precise temporal boundaries. To this end, we design a novel Convolutional-De-Convolutional (CDC) network that places CDC filters on top of 3D ConvNets, which have been shown to be effective for abstracting action semantics but reduce the temporal length of the input data. The proposed CDC filter performs the required temporal upsampling and spatial downsampling operations simultaneously to predict actions at the frame-level granularity. It is unique in jointly modeling action semantics in space-time and fine-grained temporal dynamics. We train the CDC network in an end-to-end manner efficiently. Our model not only achieves superior performance in detecting actions in every frame, but also significantly boosts the precision of localizing temporal boundaries. Finally, the CDC network demonstrates a very high efficiency with the ability to process 500 frames per second on a single GPU server. We will update the camera-ready version and publish the source codes online soon.Comment: IEEE Conference on Computer Vision and Pattern Recognition (CVPR), 201

Millisecond single-molecule localization microscopy combined with convolution analysis and automated image segmentation to determine protein concentrations in complexly structured, functional cells, one cell at a time

We present a single-molecule tool called the CoPro (Concentration of Proteins) method that uses millisecond imaging with convolution analysis, automated image segmentation and super-resolution localization microscopy to generate robust estimates for protein concentration in different compartments of single living cells, validated using realistic simulations of complex multiple compartment cell types. We demonstrates its utility experimentally on model Escherichia coli bacteria and Saccharomyces cerevisiae budding yeast cells, and use it to address the biological question of how signals are transduced in cells. Cells in all domains of life dynamically sense their environment through signal transduction mechanisms, many involving gene regulation. The glucose sensing mechanism of S. cerevisiae is a model system for studying gene regulatory signal transduction. It uses the multi-copy expression inhibitor of the GAL gene family, Mig1, to repress unwanted genes in the presence of elevated extracellular glucose concentrations. We fluorescently labelled Mig1 molecules with green fluorescent protein (GFP) via chromosomal integration at physiological expression levels in living S. cerevisiae cells, in addition to the RNA polymerase protein Nrd1 with the fluorescent protein reporter mCherry. Using CoPro we make quantitative estimates of Mig1 and Nrd1 protein concentrations in the cytoplasm and nucleus compartments on a cell-by-cell basis under physiological conditions. These estimates indicate a 4-fold shift towards higher values in concentration of diffusive Mig1 in the nucleus if the external glucose concentration is raised, whereas equivalent levels in the cytoplasm shift to smaller values with a relative change an order of magnitude smaller. This compares with Nrd1 which is not involved directly in glucose sensing, which is almost exclusively localized in the nucleus under high and..

ParseNet: Looking Wider to See Better

We present a technique for adding global context to deep convolutional networks for semantic segmentation. The approach is simple, using the average feature for a layer to augment the features at each location. In addition, we study several idiosyncrasies of training, significantly increasing the performance of baseline networks (e.g. from FCN). When we add our proposed global feature, and a technique for learning normalization parameters, accuracy increases consistently even over our improved versions of the baselines. Our proposed approach, ParseNet, achieves state-of-the-art performance on SiftFlow and PASCAL-Context with small additional computational cost over baselines, and near current state-of-the-art performance on PASCAL VOC 2012 semantic segmentation with a simple approach. Code is available at https://github.com/weiliu89/caffe/tree/fcn .Comment: ICLR 2016 submissio