Harmoni
Harmoni is an advanced platform for data analysis and visualization, specifically tailored to handle market research data. It excels in various tasks, including data processing, analysis, reporting, and visualization, as well as managing distribution and alerts. By automating many processes, Harmoni enables users to focus more on analyzing data rather than just processing it. This platform simplifies the sharing of critical and actionable insights with stakeholders. In an era where market research budgets are tightening while expectations continue to rise, Harmoni provides the flexibility to explore data in response to emerging questions. Additionally, it enables the integration of multiple data sources into a single, usable dataset. Supporting various data sources, such as IBM SPSSĀ®, SQL, and Microsoft Excel, as well as CSV and tab-delimited files, Harmoni ensures comprehensive compatibility. Furthermore, it seamlessly integrates with well-known market research tools like Voxco and FocusVision Decipher, enhancing its usability and effectiveness in the field. Ultimately, Harmoni empowers professionals to derive meaningful conclusions from their data in a more efficient manner.
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Vertex AI
Completely managed machine learning tools facilitate the rapid construction, deployment, and scaling of ML models tailored for various applications.
Vertex AI Workbench seamlessly integrates with BigQuery Dataproc and Spark, enabling users to create and execute ML models directly within BigQuery using standard SQL queries or spreadsheets; alternatively, datasets can be exported from BigQuery to Vertex AI Workbench for model execution. Additionally, Vertex Data Labeling offers a solution for generating precise labels that enhance data collection accuracy.
Furthermore, the Vertex AI Agent Builder allows developers to craft and launch sophisticated generative AI applications suitable for enterprise needs, supporting both no-code and code-based development. This versatility enables users to build AI agents by using natural language prompts or by connecting to frameworks like LangChain and LlamaIndex, thereby broadening the scope of AI application development.
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Geneious
Geneious Prime revolutionizes bioinformatics by transforming raw data into easy-to-understand visual formats that make sequence analysis accessible to users of all levels. This platform simplifies the sequence assembly process while also enabling effortless editing of contigs. It offers a range of annotation features that provide automatic gene prediction, identification of motifs, translation processes, and variant calling, significantly benefiting researchers. Additionally, users can perform genotyping on microsatellite traces through automated ladder fitting and peak calling, which results in detailed allele tables. The software presents visually appealing representations of annotated genomes and assemblies in a customizable sequence view, further enhancing the user experience. It also enables robust analyses of SNP variants, streamlines RNA-Seq expression assessments, and supports amplicon metagenomics. Moreover, users are empowered to design and evaluate PCR and sequencing primers, while also having the ability to build a searchable primer database tailored to their needs. Furthermore, Geneious Biologics stands out as a flexible, scalable, and secure solution that optimizes workflows specifically for antibody analysis, promoting the development of top-tier libraries and the identification of the best therapeutic candidates. This seamless integration of various tools not only boosts efficiency but also encourages innovation in the field of biological research, paving the way for groundbreaking discoveries.
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Illumina DRAGEN Secondary Analysis
The DRAGEN Secondary Analysis system from Illumina provides accurate, comprehensive, and exceptionally efficient processing of next-generation sequencing data. By leveraging a graph reference genome in combination with machine learning methodologies, it achieves outstanding precision. With a highly streamlined workflow, it can fully analyze a 34x whole human genome in roughly 30 minutes when operated on the DRAGEN server v4. Furthermore, it optimizes this process by reducing FASTQ file sizes by as much as five times. This system is proficient in handling diverse types of NGS data, such as whole genomes, exomes, methylomes, and transcriptomes. It has been designed to work seamlessly with the user's chosen platform and can scale to accommodate various needs. DRAGEN analysis is consistently recognized as a frontrunner in accuracy for detecting both germline and somatic variants, supported by its strong performance in industry competitions hosted by precisionFDA. This sophisticated analytical tool enables laboratories of all sizes and specialties to fully leverage their genomic datasets. Additionally, the integration of highly adaptable field-programmable gate array (FPGA) technology allows DRAGEN to implement hardware-accelerated genomic analysis algorithms, significantly improving its efficiency. These advancements firmly establish DRAGEN as an essential asset in the rapidly advancing realm of genomics, enabling researchers to push the boundaries of scientific discovery.
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