Jong R. Choi-Rak Choi

Seoul, Republic of Korea

Last Updated: 09/26/2026

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Found 9 publications

Comparison of exon-level copy number variants in CytoScan XON assay and next-generation sequencing in clinical samples.

Comparison of exon-level copy number variants in CytoScan XON assay and next-generation sequencing in clinical samples.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: August 09, 2023

FLT3 Internal Tandem Duplication in Patients With Acute Myeloid Leukemia Is Readily Detectable in a Single Next-Generation Sequencing Assay Using the Pindel Algorithm.

FLT3 Internal Tandem Duplication in Patients With Acute Myeloid Leukemia Is Readily Detectable in a Single Next-Generation Sequencing Assay Using the Pindel Algorithm.

Journal: Annals of laboratory medicine

Published: May 14, 2018

A patient with B-cell acute lymphoblastic leukemia with PAX5-ETV6 rearrangement with dic(9;12)(p13;p13) identified by chromosomal microarray.

A patient with B-cell acute lymphoblastic leukemia with PAX5-ETV6 rearrangement with dic(9;12)(p13;p13) identified by chromosomal microarray.

Journal: Annals of hematology

Published: January 02, 2018

Targeted gene panel and genotype-phenotype correlation in children with developmental and epileptic encephalopathy.

Targeted gene panel and genotype-phenotype correlation in children with developmental and epileptic encephalopathy.

Journal: Epilepsy research

Published: November 24, 2017

Efficient strategy for the molecular diagnosis of intractable early-onset epilepsy using targeted gene sequencing.

Efficient strategy for the molecular diagnosis of intractable early-onset epilepsy using targeted gene sequencing.

Journal: BMC medical genomics

Published: May 25, 2017

Detection of Immunoglobulin Heavy Chain Gene Clonality by Next-Generation Sequencing for Minimal Residual Disease Monitoring in B-Lymphoblastic Leukemia.

Detection of Immunoglobulin Heavy Chain Gene Clonality by Next-Generation Sequencing for Minimal Residual Disease Monitoring in B-Lymphoblastic Leukemia.

Journal: Annals of laboratory medicine

Published: November 08, 2016

Evaluation of an amplicon-based next-generation sequencing panel for detection of BRCA1 and BRCA2 genetic variants.

Evaluation of an amplicon-based next-generation sequencing panel for detection of BRCA1 and BRCA2 genetic variants.

Journal: Breast cancer research and treatment

Published: January 11, 2016

Bone marrow chimerism detection using next generation sequencing based on single nucleotide polymorphisms following liver transplantation: comparison with short tandem repeat-PCR.

Bone marrow chimerism detection using next generation sequencing based on single nucleotide polymorphisms following liver transplantation: comparison with short tandem repeat-PCR.

Journal: Annals of laboratory medicine

Published: April 20, 2015

Isochromosome 1q in childhood Burkitt lymphoma: the first reported case in Korea.

Isochromosome 1q in childhood Burkitt lymphoma: the first reported case in Korea.

Journal: Annals of laboratory medicine

Published: January 14, 2015

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Last Updated: 09/26/2026