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Sentiment analysis (SA) is an important research area in cognitive computation—thus, in-depth studies of patterns of sentiment analysis are necessary. At present, rich-resource data-based SA has been well-developed, while the more challenging and practical multi-source unsupervised SA (i.e., a target-domain SA by transferring from multiple source domains) is seldom studied. The challenges behind this problem mainly locate in the lack of supervision information, the semantic gaps among domains (i.e., domain shifts), and the loss of knowledge. However, existing methods either lack the distinguishable capacity of the semantic gaps among domains or lose private knowledge. To alleviate these problems, we propose a two-stage domain adaptation framework. In the first stage, a multi-task methodology-based shared-private architecture is employed to explicitly model the domain-common features and the domain-specific features for the labeled source domains. In the second stage, two elaborate mechanisms are embedded in the shared-private architecture to transfer knowledge from multiple source domains. The first mechanism is a selective domain adaptation (SDA) method, which transfers knowledge from the closest source domain. And the second mechanism is a target-oriented ensemble (TOE) method, in which knowledge is transferred through a well-designed ensemble method. Extensive experiment evaluations verify that the performance of the proposed framework outperforms unsupervised state-of-the-art competitors. What can be concluded from the experiments is that transferring from very different distributed source domains may degrade the target-domain performance, and it is crucial to choose proper source domains to transfer from.
相似文献Background
Endothelial progenitor cells (EPCs) are defined as a special type of stem cell that have been found to directly incorporate into injured vessels and that participate in angiogenesis and reconstruction by differentiation into endothelial cells. EPCs are widely used to therapeutically treat cardiovascular disease, limb ischemia and vascular repair. However, the role of EPCs in inflammatory diseases, especially in lung injury, is less studied.Objective
To investigate the application of EPCs to vascular repair, and the role of EPCs in acute lung injury (ALI) and acute respiratory distress syndrome (ARDS).Methods
A computer-based online search was performed in the PubMed database and Web of Science database for articles published, concerning EPCs, angiogenesis, ALI/ARDS and stem cell transplantationConclusion
EPCs have a therapeutic potential for vascular regeneration and may emerge as novel strategy for the diseases that are associated with ALI/ARDS. 相似文献Angiography derived FFR reveals good performance in assessing intermediate coronary stenosis. However, its performance under contemporary low X-ray frame and pulse rate settings is unknown. We aim to validate the feasibility and performance of quantitative flow ratio (QFR) and vessel fractional flow reserve (vFFR) under such angiograms.
MethodsThis was an observational, retrospective, single center cohort study. 134 vessels in 102 patients, with angiograms acquired under 7.5fps and 7pps mode, were enrolled. QFR (fQFR and cQFR) and vFFR were validated with FFR as the gold standard. A conventional manual and a newly developed algorithmic exclusion method (M and A group) were both evaluated for identification of poor-quality angiograms.
ResultsGood agreement between QFR/vFFR and FFR were observed in both M and A group, except for vFFR in the M group. The correlation coefficients between fQFR/cQFR/vFFR and FFR were 0.6242, 0.5888, 0.4089 in the M group, with rvFFR significantly lower than rfQFR (p?=?0.0303), and 0.7055, 0.6793, 0.5664 in the A group, respectively. AUCs of detecting lesions with FFR?≤?0.80 were 0.852 (95% CI 0.722–0.913), 0.858 (95% CI 0.778–0.917), 0.682 (95% CI 0.586–0.768), for fQFR/cQFR/vFFR in the M group, while vFFR performed poorer than fQFR (p?=?0.0063) and cQFR (p?=?0.0054). AUCs were 0.898 (95% CI 0.811–0.945), 0.892 (95% CI 0.803–0.949), 0.843 (95% CI 0.746–0.914) for fQFR/cQFR/vFFR in the A group. AUCvFFR was significantly higher in the A group than that in the M group (p?=?0.0399).
ConclusionsQFR/vFFR assessment is feasible under 7.5fps and 7pps angiography, where cQFR showed no advantage compared to fQFR. Our newly developed algorithmic exclusion method could be a better method of selecting angiograms with adequate quality for angiography derived FFR assessment.
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