Keyphrases
Next-generation Sequencing
87%
Acute Myeloid Leukemia
42%
Myelodysplastic Syndrome
36%
Next-generation Sequencing Data
31%
Tumor
30%
Merkel Cell Carcinoma
28%
Metagenomic Next-generation Sequencing (mNGS)
27%
Merkel Cell Polyomavirus (MCPyV)
25%
Whole Genome Sequencing
21%
Fluorescence in Situ Hybridization
21%
Formalin-fixed Paraffin-embedded Tissue
19%
Whole Exome Sequencing
18%
Single nucleotide Variant
17%
Tumor Protein p53 (TP53)
15%
Gene mutation
15%
Immunohistochemistry
14%
In Cancer
13%
Insertion-deletion
13%
High-grade Neuroendocrine Carcinoma
13%
Clinical Laboratory
12%
Somatic mutation
12%
RNA Sequencing (RNA-seq)
11%
Chronic Lymphocytic Leukemia
11%
Non-small Cell Lung Cancer (NSCLC)
11%
Sequence Data
11%
Acute Leukemia
10%
T Cells
10%
Breast Implant-associated Anaplastic Large Cell Lymphoma (BIA-ALCL)
10%
Myeloid Neoplasms
10%
Copy number Variation
10%
Head-and-neck Squamous Cell Carcinoma (HNSCC)
10%
DNA Sequencing
9%
Glioblastoma
9%
Leukemia
9%
Formalin-fixed
9%
B Cells
9%
Neuroendocrine Carcinoma
9%
Myeloid Malignancies
9%
Sequence Variants
8%
Somatic Variants
8%
Hybrid Capture
8%
High Sensitivity
8%
In Silico
8%
Mutant Allele Frequency
7%
College of American Pathologists
7%
Hematopoietic Stem Cells
7%
Subclone
7%
International Consensus Classification
7%
Lung Adenocarcinoma
7%
Genome Sequencing
7%
Medicine and Dentistry
Next Generation Sequencing
57%
Neoplasm
46%
Acute Myeloid Leukemia
31%
Myelodysplastic Syndrome
27%
Merkel Cell Carcinoma
27%
Merkel Cell Polyomavirus
23%
Diseases
18%
Exome Sequencing
17%
Gene Mutation
17%
Neuroendocrine Carcinoma
16%
Fluorescence in Situ Hybridization
16%
Head and Neck Squamous Cell Carcinoma
13%
Immunohistochemistry
13%
Malignant Neoplasm
12%
Formaldehyde
11%
Diagnosis
11%
Single Nucleotide Polymorphism
11%
Acute Leukemia
11%
Glioblastoma
10%
Breast Implant
10%
In Silico
10%
B-Cell Chronic Lymphocytic Leukemia
10%
RNA Sequence
10%
Pathologist
9%
Gene Fusion
9%
T Cell
9%
Morphology
8%
Biological Marker
8%
Cancer
8%
Somatics
8%
Somatic Mutation
8%
Neck
7%
Allele
7%
Non Small Cell Lung Cancer
7%
Clinical Oncology
7%
Hematopoietic Cell
7%
Epstein Barr Virus
7%
Overall Survival
7%
Anaplastic Large Cell Lymphoma
7%
Malignant Transformation
7%
Metastatic Carcinoma
7%
Minimal Residual Disease
6%
Molecular Pathology
6%
Classical Hodgkin Lymphoma
6%
microRNA
6%
Ganglioglioma
6%
Myeloproliferative Neoplasm
6%
Retinoblastoma
6%
Whole Genome Sequencing
6%
Exome
6%
Biochemistry, Genetics and Molecular Biology
Next Generation Sequencing
100%
Myeloid
40%
Genomics
29%
Gene Mutation
23%
Whole Genome Sequencing
22%
Single-Nucleotide Polymorphism
22%
Exome Sequencing
18%
Fluorescence in Situ Hybridization
13%
Allele
13%
Indel
13%
Exome
12%
Cytogenetics
12%
B Cell
11%
Hematopoietic Cell
11%
Germ Cell
10%
Germline
10%
Genetics
10%
Deep Sequencing
9%
RNA Sequence
9%
RNA
9%
Genome Sequencing
9%
Clonal Variation
8%
Clonality
8%
Overall Survival
8%
Epidermal Growth Factor Receptor
8%
Somatic Mutation
7%
Malignant Transformation
7%
MicroRNA
6%
Hematopoiesis
6%
DNA Sequence
6%
Molecular Disease
5%
Gene Fusion
5%
Mouse Model
5%
Exon
5%
Capillary Electrophoresis
5%
DNMT3A
5%
Chromosomal Rearrangement
5%
T Cell
5%
Interphase
5%
RNA Sequencing
5%
Gene Rearrangement
5%
Stromal Cell
5%