5,718 research outputs found
Beyond Correlation Filters: Learning Continuous Convolution Operators for Visual Tracking
Discriminative Correlation Filters (DCF) have demonstrated excellent
performance for visual object tracking. The key to their success is the ability
to efficiently exploit available negative data by including all shifted
versions of a training sample. However, the underlying DCF formulation is
restricted to single-resolution feature maps, significantly limiting its
potential. In this paper, we go beyond the conventional DCF framework and
introduce a novel formulation for training continuous convolution filters. We
employ an implicit interpolation model to pose the learning problem in the
continuous spatial domain. Our proposed formulation enables efficient
integration of multi-resolution deep feature maps, leading to superior results
on three object tracking benchmarks: OTB-2015 (+5.1% in mean OP), Temple-Color
(+4.6% in mean OP), and VOT2015 (20% relative reduction in failure rate).
Additionally, our approach is capable of sub-pixel localization, crucial for
the task of accurate feature point tracking. We also demonstrate the
effectiveness of our learning formulation in extensive feature point tracking
experiments. Code and supplementary material are available at
http://www.cvl.isy.liu.se/research/objrec/visualtracking/conttrack/index.html.Comment: Accepted at ECCV 201
Long-Term Visual Object Tracking Benchmark
We propose a new long video dataset (called Track Long and Prosper - TLP) and
benchmark for single object tracking. The dataset consists of 50 HD videos from
real world scenarios, encompassing a duration of over 400 minutes (676K
frames), making it more than 20 folds larger in average duration per sequence
and more than 8 folds larger in terms of total covered duration, as compared to
existing generic datasets for visual tracking. The proposed dataset paves a way
to suitably assess long term tracking performance and train better deep
learning architectures (avoiding/reducing augmentation, which may not reflect
real world behaviour). We benchmark the dataset on 17 state of the art trackers
and rank them according to tracking accuracy and run time speeds. We further
present thorough qualitative and quantitative evaluation highlighting the
importance of long term aspect of tracking. Our most interesting observations
are (a) existing short sequence benchmarks fail to bring out the inherent
differences in tracking algorithms which widen up while tracking on long
sequences and (b) the accuracy of trackers abruptly drops on challenging long
sequences, suggesting the potential need of research efforts in the direction
of long-term tracking.Comment: ACCV 2018 (Oral
Long-term Tracking in the Wild: A Benchmark
We introduce the OxUvA dataset and benchmark for evaluating single-object
tracking algorithms. Benchmarks have enabled great strides in the field of
object tracking by defining standardized evaluations on large sets of diverse
videos. However, these works have focused exclusively on sequences that are
just tens of seconds in length and in which the target is always visible.
Consequently, most researchers have designed methods tailored to this
"short-term" scenario, which is poorly representative of practitioners' needs.
Aiming to address this disparity, we compile a long-term, large-scale tracking
dataset of sequences with average length greater than two minutes and with
frequent target object disappearance. The OxUvA dataset is much larger than the
object tracking datasets of recent years: it comprises 366 sequences spanning
14 hours of video. We assess the performance of several algorithms, considering
both the ability to locate the target and to determine whether it is present or
absent. Our goal is to offer the community a large and diverse benchmark to
enable the design and evaluation of tracking methods ready to be used "in the
wild". The project website is http://oxuva.netComment: To appear at ECCV 201
Epigenetic inactivation of the miR-34a in hematological malignancies
miR-34a is a transcriptional target of p53 and implicated in carcinogenesis. We studied the role of miR-34a methylation in a panel of hematological malignancies including acute leukemia [acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL)], chronic leukemia [chronic lymphocytic leukemia (CLL) and chronic myeloid leukemia (CML)], multiple myeloma (MM) and non-Hodgkin's lymphoma (NHL). The methylation status of miR-34a promoter was studied in 12 cell lines and 188 diagnostic samples by methylation-specific polymerase chain reaction. miR-34a promoter was unmethylated in normal controls but methylated in 75% lymphoma and 37% myeloma cell lines. Hypomethylating treatment led to re-expression of pri-miR-34a transcript in lymphoma cells with homozygous miR-34a methylation. In primary samples at diagnosis, miR-34a methylation was detected in 4% CLL, 5.5% MM samples and 18.8% of NHL at diagnosis but none of ALL, AML and CML (P = 0.011). In MM patients with paired samples, miR-34a methylation status remained unchanged at progression. Amongst lymphoid malignancies, miR-34a was preferentially methylated in NHL (P = 0.018), in particular natural killer (NK)/T-cell lymphoma. In conclusion, amongst hematological malignancies, miR-34a methylation is preferentially hypermethylated in NHL, in particular NK/T-cell lymphoma, in a tumor-specific manner, therefore the role of miR-34a in lymphomagenesis warrants further study. © The Author 2010. Published by Oxford University Press. All rights reserved. For Permissions, please email: [email protected]
Siamese network based features fusion for adaptive visual tracking
© Springer Nature Switzerland AG 2018. Visual object tracking is a popular but challenging problem in computer vision. The main challenge is the lack of priori knowledge of the tracking target, which may be only supervised of a bounding box given in the first frame. Besides, the tracking suffers from many influences as scale variations, deformations, partial occlusions and motion blur, etc. To solve such a challenging problem, a suitable tracking framework is demanded to adopt different tracking scenes. This paper presents a novel approach for robust visual object tracking by multiple features fusion in the Siamese Network. Hand-crafted appearance features and CNN features are combined to mutually compensate for their shortages and enhance the advantages. The proposed network is processed as follows. Firstly, different features are extracted from the tracking frames. Secondly, the extracted features are employed via Correlation Filter respectively to learn corresponding templates, which are used to generate response maps respectively. And finally, the multiple response maps are fused to get a better response map, which can help to locate the target location more accurately. Comprehensive experiments are conducted on three benchmarks: Temple-Color, OTB50 and UAV123. Experimental results demonstrate that the proposed approach achieves state-of-the-art performance on these benchmarks
Accretion Disks Around Black Holes: Twenty Five Years Later
We study the progress of the theory of accretion disks around black holes in
last twenty five years and explain why advective disks are the best bet in
explaining varied stationary and non-stationary observations from black hole
candidates. We show also that the recently proposed advection dominated flows
are incorrect.Comment: 30 Latex pages including figures. Kluwer Style files included.
Appearing in `Observational Evidence for Black Holes in the Universe', ed.
Sandip K. Chakrabarti, Kluwer Academic Publishers (DORDRECHT: Holland
Quantum networks reveal quantum nonlocality
The results of local measurements on some composite quantum systems cannot be
reproduced classically. This impossibility, known as quantum nonlocality,
represents a milestone in the foundations of quantum theory. Quantum
nonlocality is also a valuable resource for information processing tasks, e.g.
quantum communication, quantum key distribution, quantum state estimation, or
randomness extraction. Still, deciding if a quantum state is nonlocal remains a
challenging problem. Here we introduce a novel approach to this question: we
study the nonlocal properties of quantum states when distributed and measured
in networks. Using our framework, we show how any one-way entanglement
distillable state leads to nonlocal correlations. Then, we prove that
nonlocality is a non-additive resource, which can be activated. There exist
states, local at the single-copy level, that become nonlocal when taking
several copies of it. Our results imply that the nonlocality of quantum states
strongly depends on the measurement context.Comment: 4 + 3 pages, 4 figure
Whole-genome association analysis of treatment response in obsessive-compulsive disorder.
Up to 30% of patients with obsessive-compulsive disorder (OCD) exhibit an inadequate response to serotonin reuptake inhibitors (SRIs). To date, genetic predictors of OCD treatment response have not been systematically investigated using genome-wide association study (GWAS). To identify specific genetic variations potentially influencing SRI response, we conducted a GWAS study in 804 OCD patients with information on SRI response. SRI response was classified as 'response' (n=514) or 'non-response' (n=290), based on self-report. We used the more powerful Quasi-Likelihood Score Test (the MQLS test) to conduct a genome-wide association test correcting for relatedness, and then used an adjusted logistic model to evaluate the effect size of the variants in probands. The top single-nucleotide polymorphism (SNP) was rs17162912 (P=1.76 × 10(-8)), which is near the DISP1 gene on 1q41-q42, a microdeletion region implicated in neurological development. The other six SNPs showing suggestive evidence of association (P<10(-5)) were rs9303380, rs12437601, rs16988159, rs7676822, rs1911877 and rs723815. Among them, two SNPs in strong linkage disequilibrium, rs7676822 and rs1911877, located near the PCDH10 gene, gave P-values of 2.86 × 10(-6) and 8.41 × 10(-6), respectively. The other 35 variations with signals of potential significance (P<10(-4)) involve multiple genes expressed in the brain, including GRIN2B, PCDH10 and GPC6. Our enrichment analysis indicated suggestive roles of genes in the glutamatergic neurotransmission system (false discovery rate (FDR)=0.0097) and the serotonergic system (FDR=0.0213). Although the results presented may provide new insights into genetic mechanisms underlying treatment response in OCD, studies with larger sample sizes and detailed information on drug dosage and treatment duration are needed
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Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS.
Obsessive-compulsive disorder (OCD) is a psychiatric condition characterized by intrusive thoughts and urges and repetitive, intentional behaviors that cause significant distress and impair functioning. The OCD Collaborative Genetics Association Study (OCGAS) is comprised of comprehensively assessed OCD patients with an early age of OCD onset. After application of a stringent quality control protocol, a total of 1065 families (containing 1406 patients with OCD), combined with population-based samples (resulting in a total sample of 5061 individuals), were studied. An integrative analyses pipeline was utilized, involving association testing at single-nucleotide polymorphism (SNP) and gene levels (via a hybrid approach that allowed for combined analyses of the family- and population-based data). The smallest P-value was observed for a marker on chromosome 9 (near PTPRD, P=4.13 × 10(-)(7)). Pre-synaptic PTPRD promotes the differentiation of glutamatergic synapses and interacts with SLITRK3. Together, both proteins selectively regulate the development of inhibitory GABAergic synapses. Although no SNPs were identified as associated with OCD at genome-wide significance level, follow-up analyses of genome-wide association study (GWAS) signals from a previously published OCD study identified significant enrichment (P=0.0176). Secondary analyses of high-confidence interaction partners of DLGAP1 and GRIK2 (both showing evidence for association in our follow-up and the original GWAS study) revealed a trend of association (P=0.075) for a set of genes such as NEUROD6, SV2A, GRIA4, SLC1A2 and PTPRD. Analyses at the gene level revealed association of IQCK and C16orf88 (both P<1 × 10(-)(6), experiment-wide significant), as well as OFCC1 (P=6.29 × 10(-)(5)). The suggestive findings in this study await replication in larger samples
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