3,394 research outputs found
Dynamic Adaptation on Non-Stationary Visual Domains
Domain adaptation aims to learn models on a supervised source domain that
perform well on an unsupervised target. Prior work has examined domain
adaptation in the context of stationary domain shifts, i.e. static data sets.
However, with large-scale or dynamic data sources, data from a defined domain
is not usually available all at once. For instance, in a streaming data
scenario, dataset statistics effectively become a function of time. We
introduce a framework for adaptation over non-stationary distribution shifts
applicable to large-scale and streaming data scenarios. The model is adapted
sequentially over incoming unsupervised streaming data batches. This enables
improvements over several batches without the need for any additionally
annotated data. To demonstrate the effectiveness of our proposed framework, we
modify associative domain adaptation to work well on source and target data
batches with unequal class distributions. We apply our method to several
adaptation benchmark datasets for classification and show improved classifier
accuracy not only for the currently adapted batch, but also when applied on
future stream batches. Furthermore, we show the applicability of our
associative learning modifications to semantic segmentation, where we achieve
competitive results
Visual Person Understanding through Multi-Task and Multi-Dataset Learning
We address the problem of learning a single model for person
re-identification, attribute classification, body part segmentation, and pose
estimation. With predictions for these tasks we gain a more holistic
understanding of persons, which is valuable for many applications. This is a
classical multi-task learning problem. However, no dataset exists that these
tasks could be jointly learned from. Hence several datasets need to be combined
during training, which in other contexts has often led to reduced performance
in the past. We extensively evaluate how the different task and datasets
influence each other and how different degrees of parameter sharing between the
tasks affect performance. Our final model matches or outperforms its
single-task counterparts without creating significant computational overhead,
rendering it highly interesting for resource-constrained scenarios such as
mobile robotics
Anisotropic Radial Layout for Visualizing Centrality and Structure in Graphs
This paper presents a novel method for layout of undirected graphs, where
nodes (vertices) are constrained to lie on a set of nested, simple, closed
curves. Such a layout is useful to simultaneously display the structural
centrality and vertex distance information for graphs in many domains,
including social networks. Closed curves are a more general constraint than the
previously proposed circles, and afford our method more flexibility to preserve
vertex relationships compared to existing radial layout methods. The proposed
approach modifies the multidimensional scaling (MDS) stress to include the
estimation of a vertex depth or centrality field as well as a term that
penalizes discord between structural centrality of vertices and their alignment
with this carefully estimated field. We also propose a visualization strategy
for the proposed layout and demonstrate its effectiveness using three social
network datasets.Comment: Appears in the Proceedings of the 25th International Symposium on
Graph Drawing and Network Visualization (GD 2017
Learning to Segment Microscopy Images with Lazy Labels
The need for labour intensive pixel-wise annotation is a major limitation of
many fully supervised learning methods for segmenting bioimages that can
contain numerous object instances with thin separations. In this paper, we
introduce a deep convolutional neural network for microscopy image
segmentation. Annotation issues are circumvented by letting the network being
trainable on coarse labels combined with only a very small number of images
with pixel-wise annotations. We call this new labelling strategy `lazy' labels.
Image segmentation is stratified into three connected tasks: rough inner region
detection, object separation and pixel-wise segmentation. These tasks are
learned in an end-to-end multi-task learning framework. The method is
demonstrated on two microscopy datasets, where we show that the model gives
accurate segmentation results even if exact boundary labels are missing for a
majority of annotated data. It brings more flexibility and efficiency for
training deep neural networks that are data hungry and is applicable to
biomedical images with poor contrast at the object boundaries or with diverse
textures and repeated patterns
Clinical development and regulatory points for consideration for second-generation live attenuated dengue vaccines.
Licensing and decisions on public health use of a vaccine rely on a robust clinical development program that permits a risk-benefit assessment of the product in the target population. Studies undertaken early in clinical development, as well as well-designed pivotal trials, allow for this robust characterization. In 2012, WHO published guidelines on the quality, safety and efficacy of live attenuated dengue tetravalent vaccines. Subsequently, efficacy and longer-term follow-up data have become available from two Phase 3 trials of a dengue vaccine, conducted in parallel, and the vaccine was licensed in December 2015. The findings and interpretation of the results from these trials released both before and after licensure have highlighted key complexities for tetravalent dengue vaccines, including concerns vaccination could increase the incidence of dengue disease in certain subpopulations. This report summarizes clinical and regulatory points for consideration that may guide vaccine developers on some aspects of trial design and facilitate regulatory review to enable broader public health recommendations for second-generation dengue vaccines
The Second Transmembrane Domain of P2X7 Contributes to Dilated Pore Formation
Activation of the purinergic receptor P2X7 leads to the cellular permeability of low molecular weight cations. To determine which domains of P2X7 are necessary for this permeability, we exchanged either the C-terminus or portions of the second transmembrane domain (TM2) with those in P2X1 or P2X4. Replacement of the C-terminus of P2X7 with either P2X1 or P2X4 prevented surface expression of the chimeric receptor. Similarly, chimeric P2X7 containing TM2 from P2X1 or P2X4 had reduced surface expression and no permeability to cationic dyes. Exchanging the N-terminal 10 residues or C-terminal 14 residues of the P2X7 TM2 with the corresponding region of P2X1 TM2 partially restored surface expression and limited pore permeability. To further probe TM2 structure, we replaced single residues in P2X7 TM2 with those in P2X1 or P2X4. We identified multiple substitutions that drastically changed pore permeability without altering surface expression. Three substitutions (Q332P, Y336T, and Y343L) individually reduced pore formation as indicated by decreased dye uptake and also reduced membrane blebbing in response to ATP exposure. Three others substitutions, V335T, S342G, and S342A each enhanced dye uptake, membrane blebbing and cell death. Our results demonstrate a critical role for the TM2 domain of P2X7 in receptor function, and provide a structural basis for differences between purinergic receptors. © 2013 Sun et al
Graphene Photonics and Optoelectronics
The richness of optical and electronic properties of graphene attracts
enormous interest. Graphene has high mobility and optical transparency, in
addition to flexibility, robustness and environmental stability. So far, the
main focus has been on fundamental physics and electronic devices. However, we
believe its true potential to be in photonics and optoelectronics, where the
combination of its unique optical and electronic properties can be fully
exploited, even in the absence of a bandgap, and the linear dispersion of the
Dirac electrons enables ultra-wide-band tunability. The rise of graphene in
photonics and optoelectronics is shown by several recent results, ranging from
solar cells and light emitting devices, to touch screens, photodetectors and
ultrafast lasers. Here we review the state of the art in this emerging field.Comment: Review Nature Photonics, in pres
Your space or mine? : Mapping self in time
Peer reviewedPublisher PD
Cardiosphere-derived cells suppress allogeneic lymphocytes by production of PGE2 acting via the EP4 receptor
derived cells (CDCs) are a cardiac progenitor cell population, which have been shown to possess cardiac regenerative properties and can improve heart function in a variety of cardiac diseases. Studies in large animal models have predominantly focussed on using autologous cells for safety, however allogeneic cell banks would allow for a practical, cost-effective and efficient use in a clinical setting. The aim of this work was to determine the immunomodulatory status of these cells using CDCs and lymphocytes from 5 dogs. CDCs expressed MHC I but not MHC II molecules and in mixed lymphocyte reactions demonstrated a lack of lymphocyte proliferation in response to MHC-mismatched CDCs. Furthermore, MHC-mismatched CDCs suppressed lymphocyte proliferation and activation in response to Concanavalin A. Transwell experiments demonstrated that this was predominantly due
to direct cell-cell contact in addition to soluble mediators whereby CDCs produced high levels of PGE2
under inflammatory conditions. This led to down-regulation of CD25 expression on lymphocytes via the
EP4 receptor. Blocking prostaglandin synthesis restored both, proliferation and activation (measured via CD25 expression) of stimulated lymphocytes. We demonstrated for the first time in a large animal model that CDCs inhibit proliferation in allo-reactive lymphocytes and have potent immunosuppressive activity mediated via PGE2
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