Patient-Specific Assays Based on Whole-Genome Sequencing Data to Measure Residual Disease in Children With Acute Lymphoblastic Leukemia: A Proof of Concept Study
by Arthur C, Rezayee F, Mogensen N, Saft L, Rosenquist R, Nordenskjöld M, Harila-Saari A, Tham E and Barbany G (2022) 12:899325. doi: 10.3389/fonc.2022.899325
Due to a production error, there was a mistake in Figure 6 as published. The part labels in the figure were not placed correctly. The corrected Figure 6 appears below. The publisher apologizes for this mistake.
Figure 6 (A–D) Kinetics of leukemic targets in CSF and plasma by ddPCR during treatment. (A) CSF and (B) plasma results in patient 3. (C) CSF and (D) plasma results in patient 4. Empty symbols denote trace values (1–2 positive droplets). CSF, cerebrospinal fluid; ddPCR, droplet digital PCR.
The original version of this article has been updated.
Keywords: acute lymphoblastic leukemia, liquid biopsy, disease monitoring, precision medicine, whole-genome sequencing, structural variation, technical feasibility, diagnostic performance
Citation: Frontiers Production Office (2023) Erratum: Patient-specific assays based on whole-genome sequencing data to measure residual disease in children with acute lymphoblastic leukemia: A proof of concept study. Front. Oncol. 12:1124071. doi: 10.3389/fonc.2022.1124071
Received: 14 December 2022; Accepted: 14 December 2022;
Published: 04 January 2023.
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