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Australian State/Territory : QLD
Research Topic : Molecular diagnostics
Field of Research : Gene Expression
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  • Funded Activity

    Linkage Projects - Grant ID: LP0349397

    Funder
    Australian Research Council
    Funding Amount
    $330,000.00
    Summary
    Gene Expression Profiling and de novo Transcriptome Sequencing using Geneballs. The purpose of the project is to demonstrate that bead-based technology can be used in applications that currently require DNA hybridisation in order to overcome existing deficiencies in microarray technology. By providing the capability to quickly and efficiently produce, screen and utilize biomolecule libraries of nearly unlimited size, this technology provides the key to unlock the power of genomics and proteomics .... Gene Expression Profiling and de novo Transcriptome Sequencing using Geneballs. The purpose of the project is to demonstrate that bead-based technology can be used in applications that currently require DNA hybridisation in order to overcome existing deficiencies in microarray technology. By providing the capability to quickly and efficiently produce, screen and utilize biomolecule libraries of nearly unlimited size, this technology provides the key to unlock the power of genomics and proteomics for use in real world applications. The project has two aspects. First, relatively small directed cDNA-bead libraries will be compared to known low-density cDNA microarrays to validate the technique for utility in gene expression profiling. Secondly, large libraries containing short oligonucleotide sequences will be used for de novo sequencing of a complete transcriptome. Proof-of-concept in either case will pave the way for many genomic applications and catapult the technology to 'blockbuster' status.
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    Funded Activity

    Linkage Infrastructure, Equipment And Facilities - Grant ID: LE0453920

    Funder
    Australian Research Council
    Funding Amount
    $108,680.00
    Summary
    Molecular diagnostics based on real-time polymerase chain reactions for emerging tropical infectious diseases aimed at protecting Australia from invasive diseases. The project aims to use the technique of real-time polymerase chain reaction to rapidly detect and quantify the organisms associated with emerging and re-emerging infectious diseases of man and animals. It will also be used to determine related gene expression. The equipment will be used to support a wide range of projects that req .... Molecular diagnostics based on real-time polymerase chain reactions for emerging tropical infectious diseases aimed at protecting Australia from invasive diseases. The project aims to use the technique of real-time polymerase chain reaction to rapidly detect and quantify the organisms associated with emerging and re-emerging infectious diseases of man and animals. It will also be used to determine related gene expression. The equipment will be used to support a wide range of projects that require the detection of specific RNA or DNA and it will allow the rapid, cost effective and efficient processing of either RNA or DNA from large numbers of samples. Minor variations in organisms will be detected using this equipment.
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    Funded Activity

    Linkage Infrastructure, Equipment And Facilities - Grant ID: LE0668507

    Funder
    Australian Research Council
    Funding Amount
    $260,000.00
    Summary
    Real time PCR and nanoparticle diagnostic facilities for high-throughput quantitative analysis of genomic structure and gene expression. Modern molecular tools have lead to an explosion in genome projects and unification of all areas of biology. The most basic need for such research is access to improving technologies for detecting DNA fingerprints that distinguish genetically-diverse genes, and determining which genes are "switched on" or 'off' in various situations. Real time PCR technology, .... Real time PCR and nanoparticle diagnostic facilities for high-throughput quantitative analysis of genomic structure and gene expression. Modern molecular tools have lead to an explosion in genome projects and unification of all areas of biology. The most basic need for such research is access to improving technologies for detecting DNA fingerprints that distinguish genetically-diverse genes, and determining which genes are "switched on" or 'off' in various situations. Real time PCR technology, pioneered by The University of Queensland (UQ) and Southern Cross University (SCU) using ARC funding in 1996, is now the technology of choice for much of this research. This project will provide high-throughput equipment for real time PCR, and will develop complementary high-throughput "nanoparticle" DNA genotyping technologies, with applications to medicine and agriculture.
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    Funded Activity

    Discovery Projects - Grant ID: DP0770465

    Funder
    Australian Research Council
    Funding Amount
    $1,462,000.00
    Summary
    Macrophage proteins: structure, function and e-science. The human genome was published five years ago, yet the functions of only a small fraction of the tens of thousands of encoded proteins are known. The development of smarter and faster methods for elucidating the structure and function of uncharacterised proteins is vital to a knowledge-based economy and a healthy society. The long-term benefits to the community will include fundamental new knowledge, generation of new pharmaceuticals and th .... Macrophage proteins: structure, function and e-science. The human genome was published five years ago, yet the functions of only a small fraction of the tens of thousands of encoded proteins are known. The development of smarter and faster methods for elucidating the structure and function of uncharacterised proteins is vital to a knowledge-based economy and a healthy society. The long-term benefits to the community will include fundamental new knowledge, generation of new pharmaceuticals and the development of new eScience approaches to streamline costs and efforts of research and to make science more accessible to the public.
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    Funded Activity

    Discovery Projects - Grant ID: DP0346797

    Funder
    Australian Research Council
    Funding Amount
    $255,000.00
    Summary
    Organisation, expression and diversity of the sub-telomeric regions of the ancient eukaryote, Giardia duodenalis. We propose to extend our findings on the extreme plasticity of the structure and organisation of the sub-telomeric region of the complete genome of Giardia by more extensive chromosome walking, and comparison of different isolates. These regions are subject to gene conversion, transcriptional silencing, gene mobility, recombination, variable surface protein expression, subtelomeric i .... Organisation, expression and diversity of the sub-telomeric regions of the ancient eukaryote, Giardia duodenalis. We propose to extend our findings on the extreme plasticity of the structure and organisation of the sub-telomeric region of the complete genome of Giardia by more extensive chromosome walking, and comparison of different isolates. These regions are subject to gene conversion, transcriptional silencing, gene mobility, recombination, variable surface protein expression, subtelomeric instability and the insertion of transposable elements, a dynamic balance between structural conservation and rapid evolution. This is a rare opportunity to understand the forces at work in moulding eukaryotic sub-telomeric sequences because Giardia is not constrained by sexual homogenisation and the dynamic variability is retained.
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    Funded Activity

    Discovery Projects - Grant ID: DP0209460

    Funder
    Australian Research Council
    Funding Amount
    $176,000.00
    Summary
    Evolution of nervous system patterning processes: characterisation of homologs of key Drosophila regulatory genes from the coral Acropora. Defining the common mechanisms of nervous system development is one of the major goals of modern biology, but is presently being addressed largely by comparisons between a few very advanced (and therefore specialised) animals. Comparative data from a lower animal is urgently needed, and will clarify many aspects of nervous system evolution and development. Th .... Evolution of nervous system patterning processes: characterisation of homologs of key Drosophila regulatory genes from the coral Acropora. Defining the common mechanisms of nervous system development is one of the major goals of modern biology, but is presently being addressed largely by comparisons between a few very advanced (and therefore specialised) animals. Comparative data from a lower animal is urgently needed, and will clarify many aspects of nervous system evolution and development. The pioneering work carried out on Acropora in this laboratory suggests that it is perhaps the best choice currently available for this purpose. This project will use Acropora to address fundamental questions about the evolution of nervous system developmental processes.
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    Funded Activity

    Discovery Projects - Grant ID: DP0772241

    Funder
    Australian Research Council
    Funding Amount
    $345,000.00
    Summary
    The sponge genome project and the evolution of multicellularity: using comparative genomics and developmental biology to reconstruct the first animals. Recently the entire genome from a living fossil - a sponge from the Great Barrier Reef - was sequenced (jointly supported by the ARC and US Department of Energy). As this genome is assembled and analysed, many of the fundamental biological processes that underlie the construction and evolution of all animals, including humans, will be revealed. .... The sponge genome project and the evolution of multicellularity: using comparative genomics and developmental biology to reconstruct the first animals. Recently the entire genome from a living fossil - a sponge from the Great Barrier Reef - was sequenced (jointly supported by the ARC and US Department of Energy). As this genome is assembled and analysed, many of the fundamental biological processes that underlie the construction and evolution of all animals, including humans, will be revealed. In addition, sponge genomics will fuel innovations in medicine and biotechnology. Specifically, sponges are renowned for their capacity to synthesise bioactive compounds used in drug development, and high-grade silica used for semi-conductor construction. This project will identify the gene networks controlling these biosynthetic processes.
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    Funded Activity

    Discovery Projects - Grant ID: DP0558901

    Funder
    Australian Research Council
    Funding Amount
    $370,000.00
    Summary
    The making of a sea shell: function and evolution of genes encoding calcareous architectures of phenomenal strength, purity and beauty. The mollusc shell is composed of microscopic layers of tabular calcium carbonate crystals and thin sheets of proteins with precise nanoscale architectures. This configuration produces a high-performance composite material that exceeds the present capabilities of human engineering. This integrated study will elucidate the molecular mechanisms controlling the fab .... The making of a sea shell: function and evolution of genes encoding calcareous architectures of phenomenal strength, purity and beauty. The mollusc shell is composed of microscopic layers of tabular calcium carbonate crystals and thin sheets of proteins with precise nanoscale architectures. This configuration produces a high-performance composite material that exceeds the present capabilities of human engineering. This integrated study will elucidate the molecular mechanisms controlling the fabrication of these architectures. This knowledge will contribute significantly to the development of materials for advanced electronics and energy transducers, human bone therapeutics and marine?based products such as pearls and cements, through the identification of genes underlying biofabrication networks and the development of in vitro bioproduction systems.
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