Table 1.

Summary of the study samples

CharacteristicsStudy samples
No. of BCP-ALL cases 23,  
Mean age, y 8.5 
Female/male, n 12/11 
BM blasts, mean % 89 
Molecular subgroup/WHO classification, no. of patients  
BCR::ABL1/BCP-ALL with (9;22)(q34.1;q11.2);BCR::ABL1 
ETV6::RUNX1/t(12;21)(p13.2;q22.1);ETV6::RUNX1 
HeH/hyperdiploidy 
DUX4-r/BCP-ALL with other defined genetic abnormalities 11 
scRNA-seq, no. of BCP-ALL cases (no. of cells) 23 (149 731) 
BCR::ABL1 4 (25 706) 
ETV6::RUNX1 4 (29 772) 
HeH 4 (21 346) 
DUX4-r 11 (72 907) 
scATAC-seq, no. of BCP-ALL cases (no. of nuclei) 19 (35 225) 
BCR::ABL1 3 (7 181) 
ETV6::RUNX1 4 (7 712) 
HeH 4 (3 623) 
DUX4-r 8 (15 657) 
No. of NBM samples (donors) 9 (5) 
MNC 
CD34+-enriched 
CD19+-enriched 
scRNA-seq, no. of NBM samples (no. of cells) 9 (38 815) 
MNC 3 (16 717) 
CD34+-enriched 3 (11 131) 
CD19+-enriched 3 (10 967) 
scATAC-seq, no. of NBM samples (no. of nuclei) 4 (6 667) 
MNC 3 (4 623) 
CD34+-enriched 1 (3 096) 
CharacteristicsStudy samples
No. of BCP-ALL cases 23,  
Mean age, y 8.5 
Female/male, n 12/11 
BM blasts, mean % 89 
Molecular subgroup/WHO classification, no. of patients  
BCR::ABL1/BCP-ALL with (9;22)(q34.1;q11.2);BCR::ABL1 
ETV6::RUNX1/t(12;21)(p13.2;q22.1);ETV6::RUNX1 
HeH/hyperdiploidy 
DUX4-r/BCP-ALL with other defined genetic abnormalities 11 
scRNA-seq, no. of BCP-ALL cases (no. of cells) 23 (149 731) 
BCR::ABL1 4 (25 706) 
ETV6::RUNX1 4 (29 772) 
HeH 4 (21 346) 
DUX4-r 11 (72 907) 
scATAC-seq, no. of BCP-ALL cases (no. of nuclei) 19 (35 225) 
BCR::ABL1 3 (7 181) 
ETV6::RUNX1 4 (7 712) 
HeH 4 (3 623) 
DUX4-r 8 (15 657) 
No. of NBM samples (donors) 9 (5) 
MNC 
CD34+-enriched 
CD19+-enriched 
scRNA-seq, no. of NBM samples (no. of cells) 9 (38 815) 
MNC 3 (16 717) 
CD34+-enriched 3 (11 131) 
CD19+-enriched 3 (10 967) 
scATAC-seq, no. of NBM samples (no. of nuclei) 4 (6 667) 
MNC 3 (4 623) 
CD34+-enriched 1 (3 096) 

MNC, mononuclear cells; no., number; NOS, not otherwise specified; scRNA-seq, single-cell RNA sequencing; WHO, World Health Organization.

Including 22 diagnostic samples and 1 relapse sample.

Including 1 mixed phenotype acute leukemia.

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