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    NGS Hero

    Controls & Reference Materials

    Seraseq® NGS Reference Materials

    SHOP PRODUCTS

    SeraCare’s comprehensive suite of patient-like reference materials accelerates development, streamlines validation, and ensures confidence in results of today’s demanding clinical genomics assays. Our platform agnostic, ground-truth reference materials can be used through all development phases to verify actionable and challenging variants as well as complex genomic signatures in patient samples. 

    Compatible Workflows

    • Next Generation Sequencing
    • Sanger Sequencing
    • Real-time PCR and digital PCR (dPCR)
    • Microarray

    A wide range of clinical applications

    • Somatic cancer - solid tumor, heme malignancy, immuno-oncology, and liquid biopsy
    • Reproductive health - NIPT (trisomies, microdeletion, sex chromosome aneuploidies)
    • Inherited cancer and cariomyopathy
    • Infectious disease - HIV and SARS-CoV-2

    Key Features

    • Ready-to-use reference materials covering clinically-relevant variants and all variant types - SNVs, INDELS, CNVs, and RNA fusions
    • Highly multiplexed - provide significantly more data per NGS run, saving sequencing costs
    • Available in multiple formats to suite different workflow needs - purified DNA & RNA, ctDNA, encapsulated ctDNA in plasma, and FFPE
    • Manufactured in cGMP-compliant, ISO 13485-certified facilities
    • Stringent product release testing - all variants qualified by dPCR for allele frequencies or copy numbers

    Develop and validate assays faster

    • Establish assay accuracy, precision, reproducibility, sensitivity, and LoD with confidence
    • Expedite assay design to analytical validation turnaround time without sacrificing quality

    Launch on time and on budget

    • Regulatory-compliant reference materials for analytical validation accepted by the New York State Department of Health, the FDA, and other regulatory bodies

    Ensure confidence in your results

    • Confirm detection of common, rare, and technically challenging variants at expected allele frequencies in patient samples
    • Validate measurement and reporting of complex genomic signatures and chromosomal aneuploidies
    • Ensure consistent run-after-run assay performance

    Custom Solution Capabilities

    • Expert-designed bespoke reference materials configured to meet your specific assay requirements
    • A high degree of flexibility – customized allele frequency, format, variant type, and matrix
    • Choose from a library of >400 clinically actionable variants or design your own
    • Fast project turnaround time with full traceability from sourcing through processing and delivery
    • Deep technical, quality management, and regulatory expertise to consult on projects 

    For research use only. Not for use in diagnostic procedures. 

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