26 research outputs found

    Design of a Low Micro Vibration High Precision CubeSat Reaction Wheel

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    Rolling element bearings are known to generate higher order harmonics. These harmonics can reach up to the 10th or higher engine order [1]. When wheels are used in a wide speed range, these higher order harmonics can pass and excite rotor eigenfrequencies and rotor modes, severely increasing the exported μ-vibrations at these frequencies. The amplification of these frequencies will then be governed by the quality factor (Q-factor) of the rotor. Single piece rotors have several advantages such as affordable tight tolerances, uniform mass and elimination of assembly errors, but such monolithic metallic structure feature high Q-factors. Material choice is a first way to address this [2], but damping will stay limited. To further increase the internal damping and reduce the Q-factor, Constrained layer damping is employed

    Large expert-curated database for benchmarking document similarity detection in biomedical literature search

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    Document recommendation systems for locating relevant literature have mostly relied on methods developed a decade ago. This is largely due to the lack of a large offline gold-standard benchmark of relevant documents that cover a variety of research fields such that newly developed literature search techniques can be compared, improved and translated into practice. To overcome this bottleneck, we have established the RElevant LIterature SearcH consortium consisting of more than 1500 scientists from 84 countries, who have collectively annotated the relevance of over 180 000 PubMed-listed articles with regard to their respective seed (input) article/s. The majority of annotations were contributed by highly experienced, original authors of the seed articles. The collected data cover 76% of all unique PubMed Medical Subject Headings descriptors. No systematic biases were observed across different experience levels, research fields or time spent on annotations. More importantly, annotations of the same document pairs contributed by different scientists were highly concordant. We further show that the three representative baseline methods used to generate recommended articles for evaluation (Okapi Best Matching 25, Term Frequency-Inverse Document Frequency and PubMed Related Articles) had similar overall performances. Additionally, we found that these methods each tend to produce distinct collections of recommended articles, suggesting that a hybrid method may be required to completely capture all relevant articles. The established database server located at https://relishdb.ict.griffith.edu.au is freely available for the downloading of annotation data and the blind testing of new methods. We expect that this benchmark will be useful for stimulating the development of new powerful techniques for title and title/abstract-based search engines for relevant articles in biomedical research.Peer reviewe

    Verification of data-race-freedom of a Java chat server with VeriFast

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    Even now, when computers have become a vital part of our society, software errors are still common, and their effects can be devastating. From the recent rise of multicores emerged the need for multi-threading software and a way to cope with its typical software errors such as data-races and deadlocks. This paper shows how VeriFast can be used to verify the data-race-freedom of a multi-threaded Java application, by means of a simple Java chat server example. We will cover the verification of jar files in general, how to deal with Java core classes and interfaces such as ArrayList and the specifics of verifying a multi-threaded Java application, using Thread, Runnable and Semaphore as building blocks. To achieve this, we need to take a closer look at VeriFast elements such as predicate families, predicate constructors and fractional permissions. This paper is intended as an experience report. We will conclude with some suggested improvements and possible future work.nrpages: 5status: publishe

    Four layer multi-omics reveals molecular responses to aneuploidy in Leishmania

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    Aneuploidy causes system-wide disruptions in the stochiometric balances of transcripts, proteins, and metabolites, often resulting in detrimental effects for the organism. The protozoan parasite Leishmania has an unusually high tolerance for aneuploidy, but the molecular and functional consequences for the pathogen remain poorly understood. Here, we addressed this question in vitro and present the first integrated analysis of the genome, transcriptome, proteome, and metabolome of highly aneuploid Leishmania donovani strains. Our analyses unambiguously establish that aneuploidy in Leishmania proportionally impacts the average transcript- and protein abundance levels of affected chromosomes, ultimately correlating with the degree of metabolic differences between closely related aneuploid strains. This proportionality was present in both proliferative and non-proliferative in vitro promastigotes. However, as in other Eukaryotes, we observed attenuation of dosage effects for protein complex subunits and in addition, non-cytoplasmic proteins. Differentially expressed transcripts and proteins between aneuploid Leishmania strains also originated from non-aneuploid chromosomes. At protein level, these were enriched for proteins involved in protein metabolism, such as chaperones and chaperonins, peptidases, and heat-shock proteins. In conclusion, our results further support the view that aneuploidy in Leishmania can be adaptive. Additionally, we believe that the high karyotype diversity in vitro and absence of classical transcriptional regulation make Leishmania an attractive model to study processes of protein homeostasis in the context of aneuploidy and beyond

    Four layer multi-omics reveals molecular responses to aneuploidy in Leishmania

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    Aneuploidy causes system-wide disruptions in the stochiometric balances of transcripts, proteins, and metabolites, often resulting in detrimental effects for the organism. The protozoan parasite Leishmania has an unusually high tolerance for aneuploidy, but the molecular and functional consequences for the pathogen remain poorly understood. Here, we addressed this question in vitro and present the first integrated analysis of the genome, transcriptome, proteome, and metabolome of highly aneuploid Leishmania donovani strains. Our analyses unambiguously establish that aneuploidy in Leishmania proportionally impacts the average transcript- and protein abundance levels of affected chromosomes, ultimately correlating with the degree of metabolic differences between closely related aneuploid strains. This proportionality was present in both proliferative and non-proliferative in vitro promastigotes. However, as in other Eukaryotes, we observed attenuation of dosage effects for protein complex subunits and in addition, non-cytoplasmic proteins. Differentially expressed transcripts and proteins between aneuploid Leishmania strains also originated from non-aneuploid chromosomes. At protein level, these were enriched for proteins involved in protein metabolism, such as chaperones and chaperonins, peptidases, and heat-shock proteins. In conclusion, our results further support the view that aneuploidy in Leishmania can be adaptive. Additionally, we believe that the high karyotype diversity in vitro and absence of classical transcriptional regulation make Leishmania an attractive model to study processes of protein homeostasis in the context of aneuploidy and beyond

    How differences between two <i>L</i>. <i>donovani</i> strains on 1 ‘omic layer correlate with their differences on another omic layer.

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    The plots show the pairwise correlations between the genome distance (aneuploidy), transcriptome distance, proteome distance, metabolome distance (all 78 metabolites), and differentiating metabolome distance (34 metabolites), each time calculated between 2 L. donovani strains. Each dot represents 1 comparison between two strains. With 6 strains in our experiment, there were 15 possible pairwise comparisons. The distance metric that was used is the Euclidean distance. Somy values were used directly, but transcript abundance, protein abundance or metabolite abundance were first Z-scored before calculating the distance. The top-right panels show the Pearson correlation coefficients with * = Pval <0.05, ** Pval <0.01, *** = Pval <0.001, while the bottom-left panels show the linear regressions.</p
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