University of Canberra

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  • A database of real existing adjectives that have been used to describe the noun democracy. Each individual description points to a distinctive archive that might be one publication or several hundred thousand publications large. It is in these archives where the meaning—or meanings—of a description can be found.
    Data Types:
    • Tabular Data
    • Dataset
  • Data of the IPEN Adult study from 10 countries that collected accelerometer data.
    Data Types:
    • Software/Code
    • Dataset
  • Camera trap data collected to model daily trapping rates (DTRs) of terrestrial avian species at arid zone waterholes in central Australia in relation to daily maximum temperature and days since last rainfall.
    Data Types:
    • Software/Code
    • Tabular Data
    • Dataset
  • This data set includes the number of males and females on the committees of various Australian pharmacy related organisations from 1998-2018.
    Data Types:
    • Tabular Data
    • Dataset
  • Forensic genotyping can be impeded by gamma-irradiation of biological evidence in the event of radiological crime. Oxidative effects within the mitochondria elicit greater damage to mitochondrial DNA (mtDNA) than nuclear DNA (nuDNA) at low doses. This study presents a novel approach for the assessment of nuDNA versus mtDNA damage from a comparison of genotype and quantity data, while exploring likely mechanisms for differential damage after high doses of gamma-irradiation. Liquid (hydrated) and dried (dehydrated) whole blood samples were exposed to high doses of gamma-radiation (1-50 kilogray, kGy). The GlobalFiler PCR Amplification Kit was used to evaluate short tandem repeat (STR) genotyping efficacy and nuDNA degradation; a comparison was made to mtDNA degradation measured using real-time PCR assays. Each assay was normalised before comparison by calculation of integrity indices relative to unirradiated controls. For nuDNA, a subset of autosomal STR markers were selected for relative size consistency with three mtDNA targets (86, 190 and 452 bp), including loci of low molecular weight (D2S441, ~75-110 bp), intermediate molecular weight (vWA and D1S1656, ~150-210 bp), and high molecular weight (TPOX and SE33, ~310-450 bp). For STR size groups containing multiple loci, the average peak heights of alleles for each marker were determined. Integrity indices were calculated from the peak height or quantity ratios of increasing amplicon size difference, comprising intermediate/short (Index A), long/intermediate (Index B), and long/short loci (Index C). Full STR profiles were attainable up to the highest dose, although DNA degradation was noticeable after 10 and 25 kGy for hydrated and dehydrated blood, respectively. This was manifested by heterozygote imbalance more than allele dropout. Degradation was greater for mtDNA than nuDNA, as well as for hydrated than dehydrated cells, after equivalent doses. Findings suggest that oxidative effects due to water radiolysis and mitochondrial function are dominant mechanisms of differential damage to nuDNA versus mtDNA after high-dose gamma-irradiation. While differential DNA damage was reduced by cell desiccation, its persistence after drying indicates innate differences between nuDNA and mtDNA radioresistance and/or continued oxidative effects within the mitochondria. Degradation of mtDNA is more severe after gamma-irradiation than nuDNA; this does not adversely impact on genotyping success of blood samples up to 50 kGy.
    Data Types:
    • Tabular Data
    • Dataset
  • Supplementary File S2. R script for selecting the top ancestry-informative markers based on the calculation of population differentiation potential using various metrics.
    Data Types:
    • Software/Code
    • Dataset
  • Stable isotope ratio and trace metal cncentration data for saffron samples
    Data Types:
    • Tabular Data
    • Dataset
  • These compressed directories contain fastA files of complexity-reduced genotyping by sequencing data of bacterial isolates from a public hospital in Australia. Sequencing data of a total of 165 bacterial isolates are included in these data sets of the following species: Enterococcus faecium, Staphylococcus aureus, Enterobacter cloacae complex, Citrobacter freundii, Klebsiella pneumoniae, Klebsiella oxytoca, Enterobacter asburiae, Escherichia coli, Morganella morganii, Citrobacter amalonaticus, Enterobacter aerogenes, Enterococcus faecalis, Hafnia alvei, Providencia rettgeri and Serratia marcescens. Additionally, this dataset includes sequencing results of genomic DNA of E. coli O157 (EDL 933) IRMM449 Sigma-Aldrich certified reference. All bacterial isolates were processed with the following combination of restriction enzymes: PstI with MseI, PstI with HpaII and MseI with HpaII. Some samples contain technical replicates and the certified reference contains six technical replicates. Each directory contains a Microsoft Excel Comma Separated Values File with bacterial isolate information, including an internal unique identity number (TargetID), the sample name (Genotype), material used for DNA extraction (Tissue), complexity-reduced genotyping method (Comment), and other details produced after sequencing (e.g. extract plate barcode, extract well, flowcell ID, flowcell lane). For a detailed description of how this data was obtained, please refer to the article "Identification of bacterial isolates from a public hospital in Australia using complexity-reduced genotyping (2019) Berenice Talamantes-Becerra, Jason Carling, Karina Kennedy, Michelle E. Gahan, Arthur Georges. Journal of Microbiological Methods, Volume 160, May 2019, Pages 11-19. https://doi.org/10.1016/j.mimet.2019.03.016
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    • Dataset
    • File Set
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  • Data Types:
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