Acute myeloid leukemia (AML) is caused by genetic aberrations that also govern the prognosis of patients and guide risk-adapted and targeted therapy. Genetic aberrations in AML are structurally diverse and currently detected by different diagnostic assays. This study sought to establish whole transcriptome RNA sequencing as single, comprehensive, and flexible platform for AML diagnostics. We developed HAMLET (Human AML Expedited Transcriptomics) as bioinformatics pipeline for simultaneous detection of fusion genes, small variants, tandem duplications, and gene expression with all information assembled in an annotated, user-friendly output file. Whole transcriptome RNA sequencing was performed on 100 AML cases and HAMLET results were validat...
Next generation sequencing (NGS) is routinely used for mutation profiling of acute myeloid leukemia....
Advances in sequencing technologies are giving unprecedented insights into the spectrum of somatic m...
Genetic lesions are crucial for cancer initiation. Recently, whole genome sequencing, using next gen...
Acute myeloid leukemia (AML) is caused by genetic aberrations that also govern the prognosis of pati...
Transcriptional profiling of acute leukemia, specifically by RNA-sequencing or whole transcriptome s...
Acute myeloid leukemia (AML) is an aggressive malignancy of haematopoietic stem cells driven by a we...
BACKGROUND: Patients with hematological malignancies (HMs) carry a wide range of chromosomal and mol...
© 2019 Anna QuaglieriAcute myeloid leukaemia (AML) is a cancer of the blood affecting the normal dev...
In recent years, our understanding of the molecular pathogenesis of myeloid neoplasms, including acu...
Myeloid neoplasms and acute leukemias derive from the clonal expansion of hematopoietic cells driven...
Abstract Fusion genes (FGs) are important genetic abnormalities in acute leukemias, but their variet...
The analyses carried out using 2 different bioinformatics pipelines (SomaticSniper and MuTect) on th...
The analyses carried out using 2 different bioinformatics pipelines (SomaticSniper and MuTect) on th...
BCR-ABL1–positive acute leukemia can be classified into three disease categories: B-lymphoblastic le...
Acute myeloid leukemias (AMLs) are currently genomically characterized by karyotype, fluorescence in...
Next generation sequencing (NGS) is routinely used for mutation profiling of acute myeloid leukemia....
Advances in sequencing technologies are giving unprecedented insights into the spectrum of somatic m...
Genetic lesions are crucial for cancer initiation. Recently, whole genome sequencing, using next gen...
Acute myeloid leukemia (AML) is caused by genetic aberrations that also govern the prognosis of pati...
Transcriptional profiling of acute leukemia, specifically by RNA-sequencing or whole transcriptome s...
Acute myeloid leukemia (AML) is an aggressive malignancy of haematopoietic stem cells driven by a we...
BACKGROUND: Patients with hematological malignancies (HMs) carry a wide range of chromosomal and mol...
© 2019 Anna QuaglieriAcute myeloid leukaemia (AML) is a cancer of the blood affecting the normal dev...
In recent years, our understanding of the molecular pathogenesis of myeloid neoplasms, including acu...
Myeloid neoplasms and acute leukemias derive from the clonal expansion of hematopoietic cells driven...
Abstract Fusion genes (FGs) are important genetic abnormalities in acute leukemias, but their variet...
The analyses carried out using 2 different bioinformatics pipelines (SomaticSniper and MuTect) on th...
The analyses carried out using 2 different bioinformatics pipelines (SomaticSniper and MuTect) on th...
BCR-ABL1–positive acute leukemia can be classified into three disease categories: B-lymphoblastic le...
Acute myeloid leukemias (AMLs) are currently genomically characterized by karyotype, fluorescence in...
Next generation sequencing (NGS) is routinely used for mutation profiling of acute myeloid leukemia....
Advances in sequencing technologies are giving unprecedented insights into the spectrum of somatic m...
Genetic lesions are crucial for cancer initiation. Recently, whole genome sequencing, using next gen...