We offer a full spectrum of genome data analysis and interpretation services. Our team of highly qualified experts, combined with advanced technology and techniques, ensures that your data is analyzed accurately and efficiently.
AUGMET streamlines the handling of intricate genomics datasets by offering an advanced yet user-friendly and intuitive interface, representing a cutting-edge solution to all your data management requirements.
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AUGMET incorporates cutting-edge algorithms and computational techniques to analyze genomic data rapidly and accurately. It leverages machine learning and artificial intelligence to provide detailed insights into genetic variations, disease predispositions, and potential treatment options.
AUGMET significantly reduces analysis time by optimizing computational workflows and utilizing parallel processing capabilities. This enables healthcare providers to deliver prompt and actionable results to patients, facilitating faster decision-making and personalized treatment plans.
AUGMET seamlessly integrates with existing healthcare systems, electronic health records, and clinical workflows. It enables efficient data sharing, collaboration, and integration of genomic information with other clinical data, ensuring a holistic approach to patient care.
With improved algorithms and refined data interpretation methods, AUGMET offers higher accuracy in identifying genetic variants and assessing their clinical significance. This precision allows for more reliable predictions of disease risk and treatment response, aiding in preventive strategies and personalized medicine approaches.
AUGMET makes precision genomics accessible by offering a cost-effective solution ensuring high-quality analysis, significantly optimizing resource utilization, operating on a transparent pricing model, and enabling unlimited horizontal scaling efficiently with your projects.
AUGMET is designed to accommodate the evolving landscape of genomics and healthcare. It is scalable to handle increasing volumes of genomic data and incorporates modular architecture, allowing for easy integration of future advancements in genomics research and technologies.
AUGMET offers an innovative approach to sequencing data analysis. Our platform combines intuitive user interfaces with indigenous sequencing algorithms to provide users with a streamlined and efficient analysis experience for diverse use cases.
AUGMET offers cutting-edge data visualization capabilities that transform complex genomic data into clear and insightful visual representations. With a rich set of visualization tools and techniques, AUGMET enables researchers to explore and interpret genomic data with ease. By visualizing genetic variations, gene expression patterns, and genomic interactions, scientists can uncover hidden patterns, identify potential biomarkers, and gain a deeper understanding of complex biological processes. AUGMET's interactive and customizable visualizations provide an intuitive way to navigate and analyze large-scale genomic datasets, empowering researchers to make informed decisions and drive breakthrough discoveries. AUGMET revolutionizes the way genomic data is analyzed and facilitates new insights into the intricacies of the genome.
We offers seamless integration with multiple leading sequencers, including MGI, Element, and Illumina, enabling researchers to streamline their genomic data analysis workflow. With full integration into these platforms, researchers can directly import sequencing data into the AUGMET, eliminating the need for manual data transfer and ensuring data integrity throughout the analysis process. This integration enables researchers to efficiently analyze large-scale genomic datasets generated by these sequencers, leveraging the AUGMET's powerful analysis capabilities.
AUGMET offers powerful reporting and export functionalities that enhance the dissemination and utilization of genomic insights. Researchers can customize and generate comprehensive reports that capture key findings, analysis parameters, and visualizations, providing a clear and concise summary of their genomic analyses. These reports can be tailored to specific audiences, whether it be fellow researchers, clinicians, or stakeholders. AUGMET also facilitates seamless data export in various formats, allowing researchers to share their findings with external collaborators or integrate the results into other analysis pipelines. This flexibility empowers researchers to leverage the outputs of the AUGMET in diverse contexts and facilitates knowledge sharing and collaboration within the scientific community. With its customizable reporting and export functionalities, AUGMET streamlines the communication of genomic insights and enables researchers to make a broader impact in the field of genomics.
>AUGMET provides comprehensive support for annotations in the fields of hematology, oncology, and germline genetics, enabling researchers to extract meaningful insights from genomic data in these critical areas. With an extensive library of curated annotations, including disease-associated variants, gene expression profiles, and functional annotations, researchers can confidently annotate and interpret genomic variants in the context of hematology, oncology, and germline genetics.
AUGMET integrates the latest knowledge and databases to ensure accurate and up-to-date annotations, empowering researchers to identify potential biomarkers, therapeutic targets, and genetic predispositions. Additionally, the AUGMET allows for interactive exploration of annotations, enabling researchers to delve deeper into the functional implications of genetic variants. By providing fully supported annotations in hematology, oncology, and germline genetics, AUGMET equips researchers with the tools they need to make informed decisions and advance precision medicine in these critical areas.
We offers advanced filtering and interpretation options that greatly enhance the analysis of functional impact in genomic data. With a range of sophisticated filtering parameters, researchers can refine their analysis and focus on variants of high relevance. AUGMET allows for customizable filters based on variant type, allele frequency, functional annotations, and pathogenicity scores, among others, enabling researchers to identify and prioritize variants with potential functional impact. Additionally, the AUGMET provides in-depth interpretation options, including variant effect prediction algorithms and pathway enrichment analysis, to unravel the biological significance of the identified variants. These interpretation tools enable researchers to understand the potential molecular mechanisms, affected pathways, and biological consequences associated with the variants, aiding in the discovery of novel disease mechanisms or therapeutic targets. With its advanced filtering and interpretation options, AUGMET empowers researchers to perform comprehensive and insightful functional impact analysis, accelerating discoveries in the realm of genomics.
AUGMET, offers a comprehensive end-to-end solution for researchers by encompassing data management, analytics capabilities, quality control (QC), analysis, annotation, reporting, and long-term storage and retrieval functionalities. With AUGMET, researchers can seamlessly manage their genomic data throughout the entire analysis workflow, ensuring data integrity and accessibility.
AUGMET offers seamless integration with Electronic Medical Records (EMR) systems, enhancing the efficiency and effectiveness of genomic analysis in clinical settings. By integrating EMR data with genomic data analysis, AUGMET enables researchers and clinicians to gain comprehensive insights into the relationship between genetic variations and patient health outcomes. The EMR integration feature of AUGMET allows researchers to access and analyze genomic data alongside patient clinical information stored within the EMR system. This integration enables researchers to correlate genomic data with patient phenotypes, medical histories, treatment responses, and outcomes. By leveraging this integrated data, researchers can identify genetic markers associated with disease susceptibility, drug responses, or treatment efficacy, leading to personalized and targeted healthcare interventions.
With AUGMET, you can seamlessly manage your genomic data from start to finish. AUGMET provides intuitive interfaces and user-friendly features that simplify data input, organization, and retrieval. You can effortlessly navigate through your data, ensuring quick access to the information you need for analysis.
AUGMET's advanced analytics capabilities enable you to uncover meaningful insights from your genomic data. You can perform complex statistical analyses, visualize data with interactive plots and visualizations, and utilize machine learning algorithms to uncover hidden patterns and relationships. AUGMET empowers you to derive valuable insights from your data, leading to breakthrough discoveries and advancements in genomics.
AUGMET, a versatile genomic data analysis platform, offers a wide range of use cases, empowering researchers, clinicians, and scientists across multiple domains. Whether you are studying genetic diseases, developing personalized therapies, or conducting population-level genomics research, AUGMET provides the tools and capabilities to drive impactful discoveries.
Having used the AUGMET Precision Genomics platform for over 2 years, I can confidently attest to its transformative impact on our clinical reporting. The platforms user-friendly UI simplifies complex analysis, ensuring streamlined and efficient genomics analysis. Its speed and reliability consistently deliver accurate results. Right from the start, I effortlessly adapted to the well-designed, intuitive interface, accessing a wide range of tools and features. The exceptional support teams expertise and responsiveness have exceeded my expectations, promptly addressing any issues or suggestions for improvement. I highly recommend AUGMET to anyone in need of a comprehensive genomics platform for clinical reporting.
We at SGRH had the pleasure of visualizing the ngs data through AUGMET. It is a good interface to visualize the data as a whole in one place. IGV images can also be seen. Significant variants can be flagged in the workbench for team interpretation, which makes it very convenient to use. Ease of variant filtration based on variant location, database availability, zygosity and internal frequency make it much more fun to use. Convenience of making gene panels based on HPO terms is another highlight of this software.
It is an easy-to-use tool for the visual exploration of genomic data including IGV images. It is very convenient. Specifically, the availability of databases makes it easier for interpretation at the same time.
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