8,099 research outputs found
Publisher Correction: Effects of porosity on dynamic indentation resistance of silica nanofoam.
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Effects of porosity on dynamic indentation resistance of silica nanofoam.
The dynamic indentation behaviors of monolithic silica nanofoams of various porosities are investigated. When the pore size is on the nm scale, as the porosity increases, despite the decrease in mass density, the resistance offered by silica nanofoam to dynamic indentation is maintained at a high level, higher than the resistance of solid silica or regular porous silica. This phenomenon is related to the fast collapse of nanocells, which produces a locally hardened region and significantly increases the volume of material involved in impact energy dissipation
Identification and analysis of candidate fungal tRNA 3'-end processing endonucleases tRNase Zs, homologs of the putative prostate cancer susceptibility protein ELAC2
<p>Abstract</p> <p>Background</p> <p>tRNase Z is the endonuclease that is responsible for the 3'-end processing of tRNA precursors, a process essential for tRNA 3'-CCA addition and subsequent tRNA aminoacylation. Based on their sizes, tRNase Zs can be divided into the long (tRNase Z<sup>L</sup>) and short (tRNase Z<sup>S</sup>) forms. tRNase Z<sup>L </sup>is thought to have arisen from a tandem gene duplication of tRNase Z<sup>S </sup>with further sequence divergence. The species distribution of tRNase Z is complex. Fungi represent an evolutionarily diverse group of eukaryotes. The recent proliferation of fungal genome sequences provides an opportunity to explore the structural and functional diversity of eukaryotic tRNase Zs.</p> <p>Results</p> <p>We report a survey and analysis of candidate tRNase Zs in 84 completed fungal genomes, spanning a broad diversity of fungi. We find that tRNase Z<sup>L </sup>is present in all fungi we have examined, whereas tRNase Z<sup>S </sup>exists only in the fungal phyla Basidiomycota, Chytridiomycota and Zygomycota. Furthermore, we find that unlike the Pezizomycotina and Saccharomycotina, which contain a single tRNase Z<sup>L</sup>, <it>Schizosaccharomyces </it>fission yeasts (Taphrinomycotina) contain two tRNase Z<sup>L</sup>s encoded by two different tRNase Z<sup>L </sup>genes. These two tRNase Z<sup>L</sup>s are most likely localized to the nucleus and mitochondria, respectively, suggesting partitioning of tRNase Z function between two different tRNase Z<sup>L</sup>s in fission yeasts. The fungal tRNase Z phylogeny suggests that tRNase Z<sup>S</sup>s are ancestral to tRNase Z<sup>L</sup>s. Additionally, the evolutionary relationship of fungal tRNase Z<sup>L</sup>s is generally consistent with known phylogenetic relationships among the fungal species and supports tRNase Z<sup>L </sup>gene duplication in certain fungal taxa, including <it>Schizosaccharomyces </it>fission yeasts. Analysis of tRNase Z protein sequences reveals putative atypical substrate binding domains in most fungal tRNase Z<sup>S</sup>s and in a subset of fungal tRNase Z<sup>L</sup>s. Finally, we demonstrate the presence of pseudo-substrate recognition and catalytic motifs at the N-terminal halves of tRNase Z<sup>L</sup>s.</p> <p>Conclusions</p> <p>This study describes the first comprehensive identification and sequence analysis of candidate fungal tRNase Zs. Our results support the proposal that tRNase Z<sup>L </sup>has evolved as a result of duplication and diversification of the tRNase Z<sup>S </sup>gene.</p
Overcoming Language Priors in Visual Question Answering via Distinguishing Superficially Similar Instances
Despite the great progress of Visual Question Answering (VQA), current VQA
models heavily rely on the superficial correlation between the question type
and its corresponding frequent answers (i.e., language priors) to make
predictions, without really understanding the input. In this work, we define
the training instances with the same question type but different answers as
\textit{superficially similar instances}, and attribute the language priors to
the confusion of VQA model on such instances. To solve this problem, we propose
a novel training framework that explicitly encourages the VQA model to
distinguish between the superficially similar instances. Specifically, for each
training instance, we first construct a set that contains its superficially
similar counterparts. Then we exploit the proposed distinguishing module to
increase the distance between the instance and its counterparts in the answer
space. In this way, the VQA model is forced to further focus on the other parts
of the input beyond the question type, which helps to overcome the language
priors. Experimental results show that our method achieves the state-of-the-art
performance on VQA-CP v2. Codes are available at
\href{https://github.com/wyk-nku/Distinguishing-VQA.git}{Distinguishing-VQA}.Comment: Published in COLING 202
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