Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Detection of recurrent, rare, and novel gene fusions in patients with acute leukemia using next‐generation sequencing approaches

25 Dec 2019

Abstract excerpt

Identification of gene fusion is an essential part in the management of patients with acute leukemia, not only for diagnosis but also in predicting the treatment outcome and selecting appropriate treatment. Adopting next-generation sequencing (NGS) technology for identification of gene fusion in patients with acute leukemia can be a good alternative to conventional tests. In the present study, the NGS RNA fusion...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Acute Lymphoblastic Leukemia research
Share to Acute Myeloid Leukemia Research
Share to Chronic Myeloid Leukemia Treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 31875988
DOI: 10.1002/hon.2709

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Detection of recurrent, rare, and novel gene fusions in patients with acute leukemia using next‐generation sequencing approachesPMID 31875988Read ↗

Detection of leukemia gene fusions by targeted RNA-sequencing in routine diagnosticsSemantic proximity Read ↗

Fusion gene map of acute leukemia revealed by transcriptome sequencing of a consecutive cohort of 1000 cases in a single centerSemantic proximity Read ↗

Identification of Novel Fusion Genes in Pediatric B-ALL patients Using Whole Transcriptome SequencingSemantic proximity Read ↗

Identification of Novel Fusion Genes in Pediatric B-ALL patients Using Whole Transcriptome SequencingSemantic proximity Read ↗

Next generation sequencing approach for detecting 491 fusion genes from human cancerSemantic proximity Read ↗

Systematic discovery of gene fusions in pediatric cancer by integrating RNA-seq and WGSSemantic proximity Read ↗

The emerging complexity of gene fusions in cancer.Semantic proximity Read ↗

Uncovering Clinically Relevant Gene Fusions with Integrated Genomic and Transcriptomic Profiling of Metastatic CancersSemantic proximity Read ↗

Clinical and molecular consequences of fusion genes in myeloid malignanciesSemantic proximity Read ↗

Fusion genes and their discovery using high throughput sequencing.Semantic proximity Read ↗

Systematic discovery of gene fusions in pediatric cancer by integrating RNA-seq and WGSSemantic proximity Read ↗

[Research Progress of Next Generation Sequencing in Acute Leukemia --Review].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.