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Full service sequencing core that provides both Sanger and Next Generation Sequencing services, in addition to library prep and quality check services, open access to equipment and training. Works directly with the bioinformatics core who can provide assist in any of your analysis needs to data storage solutions.
Facility is aimed towards developing new research tools for life sciences. In the facility, CMOS processing technologies are utilized to enable personalized healthcare and preemptive medicine via smart and miniature devices, circuits, and systems with biomedical applications. Biosensing, DNA sequencing, and smart implanting are key components of the COREs tasks. Discovery-based research and translational research is supported in this lab as the Device Fabrication facility wishes to promote the development of new research tools for life science applications.
It is based a SVM-based classifier.
Core laboratory with infrastructure and expertise to perform all aspects of protein and small molecule structure determination using X-ray crystallography. For protein structure determination, high-throughput methods are utilized to move projects rapidly from gene-to-structure.
Core supports data-enabled research through training, advising, and collaboration in data science, covering topics like research design, data access, analysis, visualization, reproducibility, ethics, and use of tools and methods in the areas of machine learning, bioinformatics, HPC, and open-source software.
Data analysis service providing a motif discovery platform developed to help biologists to find novel as well as known motifs in their peak datasets from transcription factor (TF) binding experiments such as ChIP-seq and ChIP-chip.
Knowledgebase of biomedical research resources. Repository for storing validation and problematic information about variety of entities within biomedical domain, such as antibodies, cell lines, etc. Enables researchers to submit their own claims about specific entity to make validation/problematic information F.A.I.R. (Findable, Accessable, Interoperable, Reuseable).
Core provides NMR services and instrumentation including 500MHz NMR spectrometers and X-band EPR spectrometer.
Established under the National Collaborative Research Infrastructure Strategy, the Australian National Fabrication Facility (ANFF) links 8 university-based nodes to provide researchers and industry with access to state-of-the-art fabrication facilities. The capability provided by ANFF enables users to process hard materials (metals, composites and ceramics) and soft materials (polymers and polymer-biological moieties) and transform these into structures that have application in sensors, medical devices, nanophotonics and nanoelectronics. The nodes, which are located across Australia, draw on existing infrastructure and expertise. Each offers a specific area of expertise including advanced materials, nanoelectronics & photonics and bio nano applications. Our commitment to providing a world-class user facility is underpinned by the sharing of best practice in service provision across the nodes.
Portal includes information about genetic studies of drug abuse in outbred rats. Data center created in 2014 to perform genome wide association studies on numerous behavioral traits that have well established relevance to drug abuse using outbred rats.
Software pipeline to automate centromere specific enrichment. Used for data which contain reads from the centromere. This pipeline ensures the meaningful interpretation by mapping and enrichment score assignment.
Institute for biomedical research in Barcelona, Spain.
Software tool for Bayesian analysis of single cell sequencing data. Used to perform statistical analyses of single cell RNA sequencing datasets in context of supervised experiments.
New York Genome Center (NYGC) is a nonprofit academic research institution used to drive collaborative genomic science, biomedical discovery, and clinical diagnostics
Biomedical research organization that conducts basic research on genes and proteins that control fundamental processes in living cells to analyze diseases and find keys to their causes, treatment, and prevention.
Software framework for human and nonhuman brain models.Combines open database with software for access, management, and vetting, allowing scientists to distribute their resources under FAIR principles. Supports multifaceted insight into brains across species, and enables multiverse analyses testing whether results generalize across standard references, scales.Community archive of imaging templates and atlases for improved consistency in neuroimaging R.
Software operational, evidence, provenance, and reproducibility infrastructure for the preregistered longitudinal audit of research software identity propagation across open scholarly infrastructures. This repository is research infrastructure and is not an eleventh object in the fixed ten-object study corpus.
Software Java pipeline for trimming tasks for Illumina paired end and single ended data. Flexible Trimmer for Illumina Sequence Data. Pair aware preprocessing tool optimized for Illumina next generation sequencing data. Includes several processing steps for read trimming and filtering. Operating systems Unix/Linux, Mac OS, Windows.
Source code for alpha helix structural optimisation written in MATLAB.
Core facility provides in vitro and in vivo metabolic phenotyping services. Offers expertise in experimental design and data analysis.