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Discovery Early Career Researcher Award - Grant ID: DE140100190
Funder
Australian Research Council
Funding Amount
$388,600.00
Summary
Tracing the Evolutionary History of Plant Developmental Mechanisms. Knowledge of the evolutionary history of genes involved in developmental processes provides a foundation for understanding how genetic networks were established and how their manipulation may influence plant growth and form. Genetic programs that direct growth and development in response to light will be examined functionally in Marchantia, a liverwort. Liverworts hold a key position in plant evolution as the sister group to all ....Tracing the Evolutionary History of Plant Developmental Mechanisms. Knowledge of the evolutionary history of genes involved in developmental processes provides a foundation for understanding how genetic networks were established and how their manipulation may influence plant growth and form. Genetic programs that direct growth and development in response to light will be examined functionally in Marchantia, a liverwort. Liverworts hold a key position in plant evolution as the sister group to all other land plants and possess many attributes reminiscent of the ancestral land plant. This project is expected to reveal some of the ancestral mechanisms for how light regulates plant form via the hormone auxin and could, in the future, aid the precise design of plants for diverse agricultural applications.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE150101648
Funder
Australian Research Council
Funding Amount
$363,000.00
Summary
A novel mechanism for the control of growth factor activity. Growth factors are secreted signalling molecules that govern fundamental biological processes such as cell growth, proliferation and death. The mechanism for growth factor control by a Membrane Attack Complex/Perforin-like (MACPF) protein is highly novel as MACPF proteins typically function to kill pathogens during the vertebrate immune response. This project aims to reveal how the MACPF protein Torso-like controls highly localised gro ....A novel mechanism for the control of growth factor activity. Growth factors are secreted signalling molecules that govern fundamental biological processes such as cell growth, proliferation and death. The mechanism for growth factor control by a Membrane Attack Complex/Perforin-like (MACPF) protein is highly novel as MACPF proteins typically function to kill pathogens during the vertebrate immune response. This project aims to reveal how the MACPF protein Torso-like controls highly localised growth factor signalling, using the sophisticated genetic and advanced imaging methods possible in the fruit fly Drosophila. This project aims to understand growth factor control as its deregulation leads to serious developmental disorders and diseases.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE150100652
Funder
Australian Research Council
Funding Amount
$345,000.00
Summary
Regulation of organ size and stem cell hierarchy in the developing kidney. Transient stem/progenitor cell populations play essential roles in establishing organ systems. The balance between self-renewal and differentiation in the nephron progenitor population plays a major, but poorly understood, role in regulating kidney development. Factors produced by undifferentiated progenitors promote organ expansion, whereas differentiation of these cells builds functional capacity. What is not clear is h ....Regulation of organ size and stem cell hierarchy in the developing kidney. Transient stem/progenitor cell populations play essential roles in establishing organ systems. The balance between self-renewal and differentiation in the nephron progenitor population plays a major, but poorly understood, role in regulating kidney development. Factors produced by undifferentiated progenitors promote organ expansion, whereas differentiation of these cells builds functional capacity. What is not clear is how the balance between self-renewal and differentiation is regulated in these cells, nor how the control of this fate decision impacts on optimal organ development. This project aims to dissect the molecular identity, regulation, and influence of this stem cell population on kidney development.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE230100036
Funder
Australian Research Council
Funding Amount
$465,803.00
Summary
Tracing the epigenetic life-history of cells. Each cell of the human body contains identical genetic information that is activated in different ways to form varied cell types. This research aims to develop novel single-cell genomic technologies to explain the origins of different cell types. This project expects to discover the molecular mechanisms through which specialised cell types are formed, which has been difficult to decipher using existing methods. My novel approach will elucidate how a ....Tracing the epigenetic life-history of cells. Each cell of the human body contains identical genetic information that is activated in different ways to form varied cell types. This research aims to develop novel single-cell genomic technologies to explain the origins of different cell types. This project expects to discover the molecular mechanisms through which specialised cell types are formed, which has been difficult to decipher using existing methods. My novel approach will elucidate how a small population of seemingly homogenous cells can give rise to a myriad of types of cells. Tracing the life histories of cells across time should lead to broad applications including in developmental biology, neuroscience and immunology.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE230101315
Funder
Australian Research Council
Funding Amount
$461,154.00
Summary
The dynamic interplay between the matrix and cell fate in developing heart. Malformations in the developing heart can lead to catastrophic defects and embryonic loss. The valves play a critical role in blood flow regulation and are made of a stratified matrix that is laid down early in development. This project aims to determine how the cellular fate of the early valve cells establish the layered matrix and in turn how the matrix can influence cell fate by utilising a multi-omics approach to ide ....The dynamic interplay between the matrix and cell fate in developing heart. Malformations in the developing heart can lead to catastrophic defects and embryonic loss. The valves play a critical role in blood flow regulation and are made of a stratified matrix that is laid down early in development. This project aims to determine how the cellular fate of the early valve cells establish the layered matrix and in turn how the matrix can influence cell fate by utilising a multi-omics approach to identify unique cell populations and integrate transcriptional and protein changes during matrix disruption. This project expects to generate fundamental knowledge on how matrix structure can influence cell fate in the valves and will advance Australia's knowledge base and research capabilities in developmental biology.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE120102954
Funder
Australian Research Council
Funding Amount
$375,000.00
Summary
Identifying and understanding the genetic regulators of cardiac development. The project aims to discover new genes involved in cardiac development so we can understand how to build a heart. Armed with this information, we can devise strategies for the repair of congenital and acquired heart disease.
Discovery Early Career Researcher Award - Grant ID: DE120101311
Funder
Australian Research Council
Funding Amount
$375,000.00
Summary
Role of intrinsic versus extrinsic cues in cell type determination during development and regeneration. During development all of the different cell types are generated by the action of genes and also signals from the embryo that read out which cell types are present or missing. This project studies how much environmental signals affect cell type generation developmentally and if they can be used to regenerate only the types missing in different diseases.
Discovery Early Career Researcher Award - Grant ID: DE140100217
Funder
Australian Research Council
Funding Amount
$395,220.00
Summary
Harnessing Mendel’s workhorse: meiotic crossovers for genetic diversity in crop breeding. Introducing genetic diversity from wild species into elite lines of wheat and barley may increase their resistance to the stresses they are exposed to in the field. Modern breeding cultivars could capture up to ten times more genetic variation. This project aims to gain fundamental insights into the genetic and environmental factors that limit the rates at which new genomic combinations can be made. This wi ....Harnessing Mendel’s workhorse: meiotic crossovers for genetic diversity in crop breeding. Introducing genetic diversity from wild species into elite lines of wheat and barley may increase their resistance to the stresses they are exposed to in the field. Modern breeding cultivars could capture up to ten times more genetic variation. This project aims to gain fundamental insights into the genetic and environmental factors that limit the rates at which new genomic combinations can be made. This will transform wheat and barley breeding methods, unlocking available genetic diversity to produce new varieties. Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE160100755
Funder
Australian Research Council
Funding Amount
$371,000.00
Summary
Evolution of genome architecture. The project aims to understand how changes to genome architecture over evolutionary time are linked to the diversity of animal morphology. Our genome sequence is arranged into higher order structures that enable coordinated gene expression. The appropriate expression of genes in time and space is necessary to produce the multitude of cell types that make up a multicellular organism. Yet, to date, genome topology is poorly explored, especially between species. Th ....Evolution of genome architecture. The project aims to understand how changes to genome architecture over evolutionary time are linked to the diversity of animal morphology. Our genome sequence is arranged into higher order structures that enable coordinated gene expression. The appropriate expression of genes in time and space is necessary to produce the multitude of cell types that make up a multicellular organism. Yet, to date, genome topology is poorly explored, especially between species. The project involves comparisons of the 3D structure of genomes in divergent species. These findings are expected to inform the underlying principles of gene regulation in animals and species evolution.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE140101962
Funder
Australian Research Council
Funding Amount
$395,220.00
Summary
Functional epigenomics interrogation of DNA methylation dynamics during vertebrate development and evolution. DNA methylation (mC) is an epigenetic signal essential for the maintenance of correct gene expression patterns. To investigate the causal relationships between mC and transcription during vertebrate embryonic development and evolution, this project will perform high-resolution mC profiling at different stages of teleost, amphibian and mammalian development. Highly conserved and syntenic, ....Functional epigenomics interrogation of DNA methylation dynamics during vertebrate development and evolution. DNA methylation (mC) is an epigenetic signal essential for the maintenance of correct gene expression patterns. To investigate the causal relationships between mC and transcription during vertebrate embryonic development and evolution, this project will perform high-resolution mC profiling at different stages of teleost, amphibian and mammalian development. Highly conserved and syntenic, methylated sequences will then be used as baits in proteomics screens to identify novel 5mC 'readers'. The generation of genomic profiles of mC 'readers' and their integration with developmental mC maps will reveal transient epigenome dynamics during vertebrate embryogenesis and provide new insights into the conservation of these crucial developmental mechanisms.Read moreRead less