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De-identified COVID-19 immune response data available to help accelerate solutions to the pandemic

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3,189 Samples

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Developing Therapeutic Antibodies Against COVID-19

Every immune system has a story to tell.

The key is knowing how to listen.

At Adaptive, we’re writing the next chapter of precision health — powered by immune-driven medicine.

More powerful on the inside.

Learn more

immunoSEQ Assays are for Research Use Only. Not for use in diagnostic procedures.

Put the power of even more quantitative repertoire data at your fingertips. Use your preferred sample types, now including FFPE samples.

The new immunoSEQ TCRB Kit

Same box on the outside.

Learn more

Read our press release

clonoSEQ is available as an FDA-cleared in vitro diagnostic (IVD) test service provided by Adaptive Biotechnologies for use in acute lymphoblastic leukemia and multiple myeloma patients to detect measurable residual disease (MRD) in human bone marrow samples. clonoSEQ is also available for use in other lymphoid cancers as a CLIA-regulated laboratory developed test (LDT) service provided by Adaptive Biotechnologies. clonoSEQ is only available by prescription from a licensed healthcare professional. For important information about the FDA-cleared clonoSEQ IVD test service, including the full intended use, limitations, and detailed performance characteristics, please visit clonoSEQ.com/IFU.

Medicare now covers the clonoSEQ® Assay for MRD monitoring in patients with Chronic Lymphocytic Leukemia (CLL)*

*Not FDA-cleared; available as a CLIA-regulated laboratory developed test (LDT).

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