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Field of Research : Diagnostic Applications
Research Topic : quantitative PCR
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  • Funded Activity

    A Stable Protein:DNA Complex For Development Of Ultrasensitive Diagnostics In Multiplex Format

    Funder
    National Health and Medical Research Council
    Funding Amount
    $521,961.00
    Summary
    A new technology platform will be developed to carry out diagnostic tests in a multiplex format with increased sensitivity and precision. We recently discovered a very strong interaction between a protein and a particular fragment of DNA. This interaction can be tuned to enable its use for the simultaneous detection of different disease markers in a single assay. This will improve the time and space needed to perform diagnostic tests in laboratories.
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    Funded Activity

    Improving First Trimester Screening By Combining Rapid MF-PCR Of PAP Smears With Nuchal Ultrasound Scanning

    Funder
    National Health and Medical Research Council
    Funding Amount
    $206,809.00
    Summary
    Genetic defects are the major cause of embryonic and foetal death as well as being responsible for a large proportion of childhood disabilities. Although many are detected by the ~50,000 prenatal tests currently performed annually in Australia, these methods are only offered to high risk mothers because they are invasive (~1% risk of miscarriage), and-or expensive. A rapid, low cost, less invasive and safer alternative prenatal diagnostic method such as PAP smears that could be offered to all mo .... Genetic defects are the major cause of embryonic and foetal death as well as being responsible for a large proportion of childhood disabilities. Although many are detected by the ~50,000 prenatal tests currently performed annually in Australia, these methods are only offered to high risk mothers because they are invasive (~1% risk of miscarriage), and-or expensive. A rapid, low cost, less invasive and safer alternative prenatal diagnostic method such as PAP smears that could be offered to all mothers regardless of risk is therefore of immense value both to mothers and to the health care system. This proposal enhances first trimester screening by improving prenatal diagnosis from PAP smears. Although normally taken to detect cancer, these smears contain significant numbers of foetal cells. We will investigate: the best way and time to obtain these cells, the best way to remove the cells from any contamination, improvements in genetic diagnosis of these cells using a technique known as MF-PCR which is rapidly revolutionising conventional prenatal diagnosis. By automating these procedures, they will become less expensive and more accessible to all mothers regardless of risk. We will also compare these procedures with alternative first trimester screening techniques such as nuchal translucency to determine the value of both tests singly and in combination. This research should provide a safe, reliable and accurate method allowing inexpensive prenatal screening to be available for all pregnancies. General screening programmes using this new test, particularly if combined with nuchal translucency programmes, would result in a dramatic reduction in affected babies with major implications to families and the health care system.
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    Funded Activity

    Linkage Projects - Grant ID: LP0347827

    Funder
    Australian Research Council
    Funding Amount
    $90,000.00
    Summary
    Identification of Traits and Function by Genomic Matching. Differences between individuals are largely inherited and therefore encoded within the DNA. The challenge is to develop practical means of detecting these differences irrespective of whether they are observable as a phenotype. Here we focus on livestock. For example, most Australian cattle are horned rather than polled. The inheritance is relatively simple but there is still no DNA test to detect the recessive horning gene. T .... Identification of Traits and Function by Genomic Matching. Differences between individuals are largely inherited and therefore encoded within the DNA. The challenge is to develop practical means of detecting these differences irrespective of whether they are observable as a phenotype. Here we focus on livestock. For example, most Australian cattle are horned rather than polled. The inheritance is relatively simple but there is still no DNA test to detect the recessive horning gene. The genomic matching technique is an in-house patented procedure for identifying such DNA differences. If successful, our test will assist industry to eliminate horning and thereby painful dehorning whilst reducing damage to workers and product.
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    Funded Activity

    Linkage Projects - Grant ID: LP0234452

    Funder
    Australian Research Council
    Funding Amount
    $135,270.00
    Summary
    The Relevance of the Bovine Major Histocompatibility Complex (MHC) to Milk Production. The objective of this project is to provide the dairy industry with an integrated package that includes a ?dairy performance database? linked to DNA-based information to complement existing breeding practices. Our intention is increase the profitability of the dairy industry, hence making a dairy farm a sustainable venture in a deregulated environment. Profitability results from a combination of several fact .... The Relevance of the Bovine Major Histocompatibility Complex (MHC) to Milk Production. The objective of this project is to provide the dairy industry with an integrated package that includes a ?dairy performance database? linked to DNA-based information to complement existing breeding practices. Our intention is increase the profitability of the dairy industry, hence making a dairy farm a sustainable venture in a deregulated environment. Profitability results from a combination of several factors. The drivers of the industry include political, market, environmental, husbandry, nutrition, and genetic factors. These factors are interrelated. In this proposal, we are specifically interested in the relationship between milk yields and the DNA profile of dairy cattle.
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    Showing 1-4 of 4 Funded Activites

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