122 research outputs found

    Semantic Tagging with Deep Residual Networks

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    We propose a novel semantic tagging task, sem-tagging, tailored for the purpose of multilingual semantic parsing, and present the first tagger using deep residual networks (ResNets). Our tagger uses both word and character representations and includes a novel residual bypass architecture. We evaluate the tagset both intrinsically on the new task of semantic tagging, as well as on Part-of-Speech (POS) tagging. Our system, consisting of a ResNet and an auxiliary loss function predicting our semantic tags, significantly outperforms prior results on English Universal Dependencies POS tagging (95.71% accuracy on UD v1.2 and 95.67% accuracy on UD v1.3).Comment: COLING 2016, camera ready versio

    Semantic Tagging with Deep Residual Networks

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    Semantic Tagging with Deep Residual Networks

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    Comparison Campaign of VLBI Data Analysis Software - First Results

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    During the development of the Vienna VLBI Software VieVS at the Institute of Geodesy and Geophysics at Vienna University of Technology, a special comparison setup was developed with the goal of easily finding links between deviations of results achieved with different software packages and certain parameters of the observation. The object of comparison is the computed time delay, a value calculated for each observation including all relevant models and corrections that need to be applied in geodetic VLBI analysis. Besides investigating the effects of the various models on the total delay, results of comparisons between VieVS and Occam 6.1 are shown. Using the same methods, a Comparison Campaign of VLBI data analysis software called DeDeCC is about to be launched within the IVS soon

    On the Analysis of VLBI Observations to GNSS Satellites

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    Space geodetic techniques such as Very Long Baseline Interferometry (VLBI) and Global Navigation Satellite Systems (GNSS) are used for the determination of celestial and terrestrial reference frames and Earth orientation parameters. It is of utmost importance to combine the observations from the different techniques to fully exploit the strengths and unique characteristics of the techniques, however, inaccurate local ties are problematic for a rigorous combination. To improve the link between the techniques, tests are under way to observe GNSS signals with VLBI radio telescopes directly, and to observe GNSS signals in GNSS antennas with subsequent processing in the VLBI system (“GNSS-VLBI Hybrid System”) including VLBI correlation. In both cases, the GNSS data type is the difference between the ranges from two stations to a satellite. However, it is still difficult to acquire those observations and thus we apply post-processed range measurements from a precise point positioning (PPP) solution with the C5++ software to build those single differences which are then used in the Vienna VLBI Software (VieVS). We use the CONT11 data set with identical clocks at seven sites to validate the models in VieVS and to assess the impact of the combined solution on the geodetic products

    Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V

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    Keratosis follicularis spinulosa decalvans (KFSD) is a rare cornification disorder with an X-linked recessive inheritance in most cases. Pathogenic variants causing X-linked KFSD have been described in MBTPS2, the gene for a membrane-bound zinc metalloprotease that is involved in the cleavage of sterol regulatory element binding proteins important for the control of transcription. Few families have been identified with an autosomal dominant inheritance of KFSD. We present two members of an Austrian family with a phenotype of KFSD, a mother and her son. The disease was not observed in her parents, pointing to a dominant inheritance with a de novo mutation in the index patient. Using whole-exome sequencing, we identified a heterozygous missense variant in CST6 in DNA samples from the index patient and her affected son. In line with family history, the variant was not present in samples from her parents. CST6 codes for cystatin M/E, a cysteine protease inhibitor. Patient keratinocytes showed increased expression of cathepsin genes CTSL and CTSV and reduced expression of transglutaminase genes TGM1 and TGM3. A relative gain of active, cleaved transglutaminases was found in patient keratinocytes compared to control cells. The variant found in CST6 is expected to affect protein targeting and results in marked disruption of the balance between cystatin M/E activity and its target proteases and eventually transglutaminases 1 and 3. This disturbance leads to an impairment of terminal epidermal differentiation and proper hair shaft formation seen in KFSD
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