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Scientists from the Weizmann Institute isolate rare circulating hematopoietic stem cells and apply single-cell genetic sequencing in a blood test to detect myelodysplastic syndrome and assess leukemia risk, potentially replacing bone marrow biopsy and enabling earlier intervention.

Key points

  • Teams at the Weizmann Institute capture rare circulating CD34+ hematopoietic stem cells in peripheral blood.
  • Single-cell genetic sequencing identifies somatic mutations linked to myelodysplastic syndrome and leukemia.
  • Blood‐based assay predicts MDS severity and leukemia risk, replacing invasive bone marrow biopsy.

Why it matters: A noninvasive blood test for early leukemia risk could transform diagnosis, enabling timely therapy and reducing reliance on invasive bone marrow biopsies.

Q&A

  • What is myelodysplastic syndrome?
  • Why are circulating stem cells important?
  • How does single-cell genetic sequencing work?
  • What is clonal hematopoiesis?
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