Our Technology
Drive Precision Medicine Forward
Our end-to-end software solution empowers your lab to operate at the efficiency of a large team, without the overhead, ensuring scalability and cost-effectiveness.
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Identifying and managing integration points (seams) is crucial for a successful, enterprise-wide precision medicine program.
The BioBeam Platform empowers pathology departments to transform raw data into consistent, actionable insights while ensuring unified and secure access to your data at every stage of the workflow.
By eliminating the need to acquire and integrate disparate software solutions from multiple vendors, BioBeam simplifies operations, enhancing scalability and flexibility. This streamlined approach removes barriers to test menu adoption and growth, enabling pathology labs to focus on delivering high-quality care.
Our solution manages every aspect of a next-generation molecular laboratory, from accession and processing to clinical decision support and final, customizable case signout. BioBeam supports both somatic and germline testing, providing labs with the tools needed for comprehensive molecular diagnostics. With centralized access to your data, BioBeam provides the transparency and control needed to make impactful decisions and achieve better patient outcomes.
Wet Lab Management: Streamlines sample tracking, workflows, and bioinformatics integration for seamless data processing and reporting
BioBeam LIMS
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Order entry.
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Patient/case/specimen/nucleic acid management.
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Wet lab procedures.
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Bioinformatics pipeline integration enables interpretation and reporting of clinical results and sequencing data.
Streamlined NGS Data Processing: BLI provides labs with one-click bioinformatics pipelines for transforming the tsunami of NGS data into an easy-to-understand report.
BioBeam
Pipelines
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Integration with various sequencers (Illumina, MGI, Element, etc) to pull raw run data and perform BLI’s bioinformatics pipeline and ensure comprehensive data standardization.
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Automate preprocessing, quality control, and alignment for NGS data, tailored for both somatic and germline testing to accommodate diverse laboratory needs.
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Leverage AI-driven algorithms for faster and more accurate variant calling, including specialized modules for detecting and interpreting germline mutations that are crucial for hereditary risk assessments and genetic counseling.
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Enable seamless annotation of genomic variants using integrated clinical databases, enhancing the accuracy and clinical relevance of somatic as well as germline variant reports.
Pathologist Decision Support: Vetting involves evaluating available evidence to determine the impact of each variant and if it should be reported.
BioBeam VarSuite
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Database storage of annotated variants from BioBeam Pipelines, including comprehensive support for both somatic and germline variants, ensuring robust data management across all testing types.
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Retrieval and viewing of case-level variant sets, allowing for detailed examination of somatic mutations and hereditary variations.
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Management tools to set variant filter rules and define cutoffs, tailored to the specific requirements of both somatic and germline analyses.
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Access to previously signed out data & population/disease-specific database, clinical variant databases, and leading knowledge bases: OncoKB and CKB Boost.
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Data visualization of copy number variant plots and other critical genetic markers to facilitate the sign-out process, supporting effective decision-making for patient care.
Dynamic and Personalized Clinical Reporting: Provides a pathology department with a modern technology stack that is flexible, extendible, and scalable.
BioBeam
Reporting
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Tailored report capabilities, including real-time editing and customizable templates for both somatic and germline test results.
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Rule-based reporting: integrations with Genomenon's Cancer Knowledgebase (CKB) for cutting-edge somatic insights and your own custom knowledge base to include significant germline findings, enabling comprehensive genomic interpretation.
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​Multi-language support to accommodate diverse patient demographics and enhance the accessibility of complex genetic data.
Unlocking Insights from Molecular Data: Provides a centralized platform for managing, visualizing, and analyzing molecular data with real-time insights, AI-driven tools, and scalable infrastructure for precision medicine and research.
BioBeam
Analytics
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A centralized repository for all molecular data, enabling downstream research and analytics.
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Tools for comprehensive visualization of genomic trends and variant distributions.
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Enable real-time processing and analytics for laboratory QC & data science teams.
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Identify anomalies and outliers in genomic data with Dashboards and AI.