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. 2021 Jul 8;106(11):3004–3007. doi: 10.3324/haematol.2021.278762

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Copyright© 2021 Ferrata Storti Foundation

This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 4.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.

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Figure 2. — RUNX1 database genomics cohort demographic. (A) Breakdown of the number and types of NGS samples currently stored in the RUNX1db. Pre- Leukemic: thrombocytopenia, asymptomatic Other: includes post-transplant/post-treatment and saliva samples. Both WES and panel data is analysed and stored in the database. (B) Scatter plot displaying the age of the individual when each sample was collected. Major RUNX1db cohorts (malignancy and preleukemic samples) are displayed. The median age for each cohort is represented by the vertical line. Clinical demographics of the malignancy cohort is shown with the number of individuals with different types of FPD-MM malignancy presentation and the (C) gender and (D) age distribution; Adult ≥40years, AYA=15-39 years, children ≤14years. AML: Acute myeloid leukemia; MDS: myelodysplastic syndromes; MDS/MPN: myelodysplastic syndrome/myeloproliferative Neoplasm overlap; MPN: Myeloproliferative Neoplasm; ALL: acute lymphoblastic leukemia; AL: acute undifferentiated leukemia.