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seek and you will find

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    • LeukoPrint
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      • PanCanSeek
    • Publication 
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  • PanCanSeekTM

    Comprehensive Solutions for Hematological Malignancies: Genetics and Molecular Diagnostics

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    PanCanSeek™ utilizes whole-genome sequencing (50×) of bone marrow cell DNA to offer comprehensive genomic profiling. By capturing four types of genomic variants, including structural variants (SVs), copy number aberrations (CNAs), copy number neutral loss of heterozygosity (CN-LOH), and single nucleotide variations (SNVs and InDels), this approach enables clinicians to conduct accurate molecular typing, effective prognostic stratification, and precise therapeutic guidance.

  • One for All

    PanCanSeekTM, one test to detect four types of genetic variations across the entire genome.

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  • Specifications

    ◉ Indicated subjects:Patients suspected or diagnosed with hematologic malignancies

    ◉ Sample requirement:2ml bone marrow

    ◉ Result readout:SV, CNA, CN-LOH, SNV, and InDel

    ◉ Turnaround time (TAT):15 working days

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    How it works

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    Customer order

    Customers can place orders through SeekIn official website or local agents

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    Blood-draw

    2ml bone marrow collected in EDTA tubes and ransport under refrigeration

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    Testing

    Detection by next generation sequencing (NGS) platform

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    Reporting

    The test results will be ready in about 15 workdays after your blood draw arrived at central lab

  • Please review the instructions to gain a better understanding of PanCanSeekTM and assess whether it meets your needs.

    Downlod the Instructions

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