2021
DOI: 10.3390/cancers13123001
|View full text |Cite
|
Sign up to set email alerts
|

Next Generation Cytogenetics in Myeloid Hematological Neoplasms: Detection of CNVs and Translocations

Abstract: Conventional cytogenetics are the gold standard for the identification of chromosomal alterations recurrent in myeloid neoplasms. Some next-generation sequencing (NGS) panels are designed for the detection of copy number variations (CNV) or translocations; however, their use is far from being widespread. Here we report on the results of a commercial panel including frequent mutations, CNVs and translocations in myeloid neoplasms. Frequent chromosomal alterations were analyzed by NGS in 135 patients with myeloi… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2022
2022
2023
2023

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 45 publications
(54 reference statements)
0
2
0
Order By: Relevance
“…Furthermore, the detection and characterization of CNVs could help in monitoring the prognosis of patients with hematologic malignancies such as ALL [ 101 ]. Although WGS improved the efficiency of detecting chromosomal alterations in various hematologic disorders [ 102 ], detecting CNVs can be challenging because they can be difficult to distinguish from noise in sequencing data.…”
Section: Ai-assisted Genomic Testing For Hematologic Disordersmentioning
confidence: 99%
“…Furthermore, the detection and characterization of CNVs could help in monitoring the prognosis of patients with hematologic malignancies such as ALL [ 101 ]. Although WGS improved the efficiency of detecting chromosomal alterations in various hematologic disorders [ 102 ], detecting CNVs can be challenging because they can be difficult to distinguish from noise in sequencing data.…”
Section: Ai-assisted Genomic Testing For Hematologic Disordersmentioning
confidence: 99%
“…NGS approaches including CNV may be interesting as a complementary technique to karyotype and FISH. Therefore, it would be advisable to include probes and bioinformatic algorithms to allow their analysis in AML panels [18]. This type of analysis may extend fast due to the growing body of evidence pointing to CNVs as clinically relevant in AML.…”
Section: Gene Panelsmentioning
confidence: 99%