Northstar Select CH™

Avoid false signals from clonal hematopoiesis (CH).

>99%

accuracy on CH calling for clinically actionable variants1

Introducing a panel-wide CH filter powered by ultra-sensitive buffy-coat (WBC) sequencing of CH-prone, clinically actionable genes recommended by guidelines2,3, with proprietary machine-learning classification for all other genes.

What is Clonal Hematopoiesis (CH)?

CH is primarily a natural, age-related accumulation of somatic mutations in hematopoietic stem cells. Also termed ‘CH of indeterminate potential’ (CHIP), this refers to certain driver mutations that are derived from non-tumor origins.4

Solid tumor patients harbors at least one CH-derived alteration5
Observed frequency of CH in PARPi genes (e.g. CHEK2)6

Treat with confidence.

The prevalence varies by tumor type and can occur at a wide range of VAF. Proper attribution is critical, as non–tumor-derived alterations are not expected to respond to targeted therapies in the same way as true somatic tumor mutations, potentially exposing patients to unnecessary toxicity and ineffective treatment.

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For clinically actionable DNA repair genes (PARPi genes), buffy-coat (white blood cell) sequencing is recommended in guidelines2,3 to rule out CH.

How Northstar Select CH™ works

Northstar Select CH™ is designed to seamlessly integrate into the existing Northstar Select® testing workflow, as an add-on test at the time of initial order

Powered by buffy-coat sequencing
For CH-prone genes, and proprietary machine-learning classification for all others
Covers copy number amplifications (19 genes) and copy number losses (5 genes)
Achievable through the online portal or TRF - seamless integration with Northstar Select Reporting

What clinicians receive

Unparalleled accuracy

with panel-wide assessment of CH

Clear differentiation

between tumor-derived and CH-derived variants

Improved confidence

in clinically actionable findings

Seamless delivery

of CH insights as part of the Northstar Select Report

  • BillionToOne internal data on file, Jan 2026

  • Pascual, J., et al. ESMO recommendations on the use of ctDNA assays... Ann Oncol. 2022 Aug;33(8):750-768. PMID: 35809752.

  • Lockwood, CM., et al. A Joint Consensus Recommendation of AMP and CAP... Mol Diagn. 2023 Dec;25(12):876-897. doi: 10.1016/j.jmoldx.2023.09.004. Epub 2023 Oct 6. PMID: 37806433.

  • Marshall CH, et al. Cancer Res. 2022 Nov 15;82(22):4107-4113. PMID:36040522.

  • Coombs, CC., et al. Cell Stem Cell. 2017 Sep 7;21(3):374-382.e4. Epub 2017 Aug 10. PMID: 28803919

  • Magee D, et al. Clin Cancer Res. 2025 Jul 1;31(13):2710-2718. PMID: 39932457.

More answers start here.

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