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BLOOD
Plasma and buffy coat
Banked plasma and matched buffy coat for comparison with the same donor’s tumor tissue. The team reviews collection and processing records against your analyte and assay requirements.
LIQUID BIOPSY & MCED
Patient-matched plasma, buffy coat, and tumor tissue for liquid biopsy and oncology biomarker research. Source banked sets or plan a collection around your cohort, treatment status, and protocol.
Explore matched sets
WHAT WE DO
Liquid biopsy development and oncology biomarker research depend on access to patients across disease stages, treatment histories, and demographic groups. Study cohorts should reflect the population your diagnostic or therapy is intended to serve.
Our physician network recruits and collects to your protocol. You define the cohort; we connect your study with eligible patients and coordinate specimen collection.
MATCHED SPECIMEN SETS
Patient-matched specimens let you compare findings across plasma, buffy coat, and tumor tissue from the same donor, supporting biomarker discovery, concordance studies, and oncology drug development.
BLOOD
Banked plasma and matched buffy coat for comparison with the same donor’s tumor tissue. The team reviews collection and processing records against your analyte and assay requirements.
TUMOR TISSUE
FFPE tumor tissue for histologic and molecular assessment, with frozen tissue included in selected sets. Compare tissue findings with the matched plasma result.
Selected inventory by cancer diagnosis and specimen type. Download the full workbook for donor-level details and quantities.
| Clinical diagnosisRecorded pathology | Blood | Tumor tissue | ||
|---|---|---|---|---|
| Plasma | Buffy coat | FFPE tissue | Frozen tissue | |
| Breast CancerInvasive Ductal Carcinoma (IDC) | Plasma | Buffy coat | FFPE tissue | Frozen tissue |
| Colorectal CancerAdenocarcinoma | Plasma | Buffy coat | FFPE tissue | Frozen tissue |
| Ovarian CancerPapillary Cystoadenocarcinoma | Plasma | Buffy coat | FFPE tissue | Frozen tissue |
| Prostate CancerAdenocarcinoma | Plasma | Buffy coat | FFPE tissue | Frozen tissue |
| Renal cancerClear Cell Carcinoma | Plasma | Buffy coat | FFPE tissue | Frozen tissue |
| LymphomaNon-Hodgkin's Lymphoma | Plasma | Buffy coat | FFPE tissue | Frozen tissue |
Invasive Ductal Carcinoma (IDC)
Adenocarcinoma
Papillary Cystoadenocarcinoma
Adenocarcinoma
Clear Cell Carcinoma
Non-Hodgkin's Lymphoma
Individual sets differ. Availability, quantities, and case details are confirmed for each request.
COHORT DESIGN
For early-detection work, define healthy, benign, and cancer cohorts around the intended-use population. We scope eligibility and collection for each group.
Reference comparisons
Define eligibility and clinical-review criteria for reference specimens used to assess false-positive rates.
Nonmalignant conditions
Include relevant benign conditions to evaluate how the assay distinguishes them from cancer-associated findings.
Disease-associated findings
Define cohorts by indication, stage, and treatment status to study the signals your assay measures.
Define demographic matching and treatment-naive requirements across the cohorts. Plan consistent collection and handling to reduce pre-analytical variation.
CUSTOM COLLECTION
Work with the Biospecimen Solutions team to plan a direct collection through our physician network in the United States and Latin America. For tumor-adjacent normal tissue, other specimen types, or different combinations, we scope a protocol-specific collection.
Indication, stage, treatment status, and donor demographics, including requirements for treatment-naive cohorts.
Tube type, processing windows, centrifugation, and storage, specified for the analyte and assay. Discuss requirements for ctDNA, cfRNA, methylation, and fragmentomics.
Required clinical fields, collection timepoints, blood-to-tissue timing, and pathology review, captured per protocol.
Discuss your protocol for these and other indications.
Diagnosis, histology, tumor grade, and stage.
Age, gender, and ethnicity, as recorded in the inventory.
Specimen type, collection date, and recorded quantity.
Direct collections follow IRB/IEC oversight, informed consent, and documented chain of custody. De-identified specimens and clinical data are supplied according to the agreed protocol.
EXPERIENCE
Work with a biospecimens team experienced in the collection requirements, clinical data, and specimen handling that diagnostic and drug development demand.
Biospecimens team experience
20+
Years in biospecimens
9M+
Specimens
800+
Programs
DCN Dx maintains ISO 13485- and ISO 9001-certified quality systems.
REQUEST SPECIMENS
Share your indication, specimen types, cohort criteria, quantities, and timing. The team will review banked matched sets or plan a direct collection.
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Include stage, treatment status, or donor criteria, if relevant.
Please enter the specimen types you need.
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