Error-corrected next-generation sequencing for profiling the subclonal genetic architecture of juvenile myelomonocytic leukemia
- 7 April 2026
- journal article
- Published by Springer Nature in Leukemia
- Vol. 40 (5) , 1035-1039
Abstract
No abstract availableFunding Information
- Japan Agency for Medical Research and Development (22ck0106611h0003)
- Japan Agency for Medical Research and Development (23ck0106855h0001)
- Japan Society for the Promotion of Science (21K07771)
- Donation from Nagoya Pediatric Cancer Fund.
This publication has 12 references indexed in Scilit:
- Defining the KRAS- and ERK-dependent transcriptome in KRAS-mutant cancersScience, 2024
- Detection of subclonal SETBP1 and JAK3 mutations in juvenile myelomonocytic leukemia using droplet digital PCRLeukemia, 2020
- Integrated molecular profiling of juvenile myelomonocytic leukemiaBlood, 2018
- Enhancing the accuracy of next-generation sequencing for detecting rare and subclonal mutationsNature Reviews Genetics, 2018
- Genome-wide DNA methylation is predictive of outcome in juvenile myelomonocytic leukemiaNature Communications, 2017
- RAS-pathway mutation patterns define epigenetic subclasses in juvenile myelomonocytic leukemiaNature Communications, 2017
- Juvenile myelomonocytic leukemia displays mutations in components of the RAS pathway and the PRC2 networkNature Genetics, 2015
- The genomic landscape of juvenile myelomonocytic leukemiaNature Genetics, 2015
- Subclonal mutations in SETBP1 confer a poor prognosis in juvenile myelomonocytic leukemiaBlood, 2015
- Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemiaNature Genetics, 2013