acute myeloid leukemia phenotype

Aliases

AML

Related entities (3)

Mentioned in (70)

Papers in which this entity is mentioned.

• A guide to transcriptomic deconvolution in cancer. (2026)
• Tumor-informed deep sequencing of ctDNA detects minimal residual disease and predicts relapse in osteosarcoma. (2024)
• A Novel Tissue-Free Method to Estimate Tumor-Derived Cell-Free DNA Quantity Using Tumor Methylation Patterns. (2023)
• Towards understandings of serine/arginine-rich splicing factors. (2023)
• RNA splicing dysregulation and the hallmarks of cancer. (2023)
• Nanopore sequencing technology, bioinformatics and applications. (2021)
• Application of third-generation sequencing in cancer research. (2021)
• Alternative splicing: Human disease and quantitative analysis from high-throughput sequencing. (2021)
• Micro-RNA-125a mediates the effects of hypomethylating agents in chronic myelomonocytic leukemia. (2021)
• NUP98-NSD1 Driven MDS/MPN in Childhood Masquerading as JMML. (2021)
• Emerging Roles of SRSF3 as a Therapeutic Target for Cancer. (2020)
• Diverse noncoding mutations contribute to deregulation of cis-regulatory landscape in pediatric cancers. (2020)
• Single-Cell RNA-Seq Reveals AML Hierarchies Relevant to Disease Progression and Immunity. (2019)
• CHASMplus Reveals the Scope of Somatic Missense Mutations Driving Human Cancers. (2019)
• Super-enhancers: critical roles and therapeutic targets in hematologic malignancies. (2019)
• Comprehensive analysis of structural variants in breast cancer genomes using single molecule sequencing (2019)
• CNVScope: Visually Exploring Copy Number Aberrations in Cancer Genomes. (2019)
• CALDER: Inferring Phylogenetic Trees from Longitudinal Tumor Samples. (2019)
• Single-cell multiomic analysis identifies regulatory programs in mixed-phenotype acute leukemia. (2019)
• Driver Fusions and Their Implications in the Development and Treatment of Human Cancers. (2018)
• Quantification of subclonal selection in cancer from bulk sequencing data. (2018)
• Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptome. (2018)
• Patterns and mechanisms of structural variations in human cancer. (2018)
• ClonEvol: clonal ordering and visualization in cancer sequencing. (2017)
• OncoKB: A Precision Oncology Knowledge Base. (2017)
• Statistical algorithms improve accuracy of gene fusion detection. (2017)
• One-Carbon Metabolism in Health and Disease. (2017)
• A Next Generation Connectivity Map: L1000 Platform and the First 1,000,000 Profiles. (2017)
• chromVAR: inferring transcription-factor-associated accessibility from single-cell epigenomic data. (2017)
• The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog). (2017)
• Tumor phylogeny inference using tree-constrained importance sampling. (2017)
• Visualizing tumor evolution with the fishplot package for R. (2016)
• Small molecule inhibition of cAMP response element binding protein in human acute myeloid leukemia cells. (2016)
• GenVisR: Genomic Visualizations in R. (2016)
• Truncating Erythropoietin Receptor Rearrangements in Acute Lymphoblastic Leukemia. (2016)
• The cell cycle regulator CCDC6 is a key target of RNA-binding protein EWS. (2015)
• What is the DNA repair defect underlying Fanconi anemia? (2015)
• The landscape of long noncoding RNAs in the human transcriptome. (2015)
• MBASED: allele-specific expression detection in cancer tissues and cell lines. (2014)
• CDK9-mediated transcription elongation is required for MYC addiction in hepatocellular carcinoma. (2014)
• Clonal evolution in hematological malignancies and therapeutic implications. (2014)
• The genomic landscape of the Ewing Sarcoma family of tumors reveals recurrent STAG2 mutation. (2014)
• THetA: inferring intra-tumor heterogeneity from high-throughput DNA sequencing data. (2013)
• Fusion genes and their discovery using high throughput sequencing. (2013)
• Mutational heterogeneity in cancer and the search for new cancer-associated genes. (2013)
• Thalidomide-a notorious sedative to a wonder anticancer drug. (2013)
• Emerging landscape of oncogenic signatures across human cancers. (2013)
• An APOBEC cytidine deaminase mutagenesis pattern is widespread in human cancers. (2013)
• Differential expression profiles of glycosphingolipids in human breast cancer stem cells vs. cancer non-stem cells. (2013)
• Proteomic and bioinformatic analysis of mammalian SWI/SNF complexes identifies extensive roles in human malignancy. (2013)
• The genomic landscape of hypodiploid acute lymphoblastic leukemia. (2013)
• Pan-cancer patterns of somatic copy number alteration. (2013)
• An Inv(16)(p13.3q24.3)-encoded CBFA2T3-GLIS2 fusion protein defines an aggressive subtype of pediatric acute megakaryoblastic leukemia. (2012)
• Molecular genetics of B-precursor acute lymphoblastic leukemia. (2012)
• Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing. (2012)
• Assessing telomeric DNA content in pediatric cancers using whole-genome sequencing data. (2012)
• Detectable clonal mosaicism from birth to old age and its relationship to cancer. (2012)
• Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations. (2012)
• A framework for regularized non-negative matrix factorization, with application to the analysis of gene expression data. (2012)
• VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. (2012)
• Regulation of chromatin by histone modifications. (2011)
• Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion. (2011)
• Allele-specific copy number analysis of tumors. (2010)
• A flexible R package for nonnegative matrix factorization. (2010)
• Integrative analysis of the melanoma transcriptome. (2010)
• MicroRNAs: master regulators of ethanol abuse and toxicity? (2010)
• Longitudinally mapping the influence of sex and androgen signaling on the dynamics of human cortical maturation in adolescence. (2010)
• BreakDancer: an algorithm for high-resolution mapping of genomic structural variation. (2009)
• Recurring mutations found by sequencing an acute myeloid leukemia genome. (2009)
• Mouse Af9 is a controller of embryo patterning, like Mll, whose human homologue fuses with Af9 after chromosomal translocation in leukemia. (2002)

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