Biochemistry, Genetics and Molecular Biology
Next Generation Sequencing
100%
Myeloid
38%
Gene Mutation
26%
IDH1
21%
Somatic Mutation
21%
Gene Fusion
20%
Epidermal Growth Factor Receptor
19%
Androgen Receptor
18%
Wart Virus
18%
KRAS
18%
Gene Frequency
16%
Germ Cell
15%
Germline
15%
Overall Survival
13%
P53
12%
Gene Expression Profiling
12%
P16
11%
Exome Sequencing
11%
Single-Nucleotide Polymorphism
11%
Alpha Thalassemia/Mental Retardation X-Linked
10%
Mutated Genes
10%
Fluorescence in Situ Hybridization
10%
Sanger Sequencing
10%
Chromosomal Translocation
10%
Multiplex Polymerase Chain Reaction
9%
Indel
9%
Genotyping
9%
Amplicon Sequencing
9%
Plant Gene
9%
Stem Cell
9%
Neuroendocrine Cell
9%
Molecular Genetics
9%
STAT6
9%
Human Papillomavirus Type 18
9%
Nucleoporin
9%
Enzalutamide
9%
Artificial Intelligence
9%
Classification
9%
Homeodomain
9%
Synaptophysin
9%
Microsatellite Instability
9%
Tumor Suppressor Gene
9%
Jumping
9%
Polymorphonuclear Cell
9%
CRISPR/Cas9
9%
Optical Genome Mapping
9%
Amplicon
8%
IDH2
7%
Mitogen-Activated Protein Kinase
7%
Codon
7%
Medicine and Dentistry
Neoplasm
51%
Next Generation Sequencing
47%
Clear Cell Renal Cell Carcinoma
37%
Eosinophilic
23%
Diagnosis
21%
Cell-Free DNA
18%
Malignant Neoplasm
18%
Osteosarcoma
18%
Gene Mutation
18%
Morphology
15%
Somatic Mutation
14%
Immunohistochemistry
14%
Fluorescence in Situ Hybridization
11%
Targeted Therapy
11%
Myeloid Malignancy
11%
Ganglioneuroblastoma
10%
Gene Fusion
10%
Somatics
10%
Formaldehyde
9%
Tuberous Sclerosis
9%
Myelodysplastic Syndrome
9%
Gamma Urogastrone
9%
Epidermal Growth Factor Receptor 2
9%
Hematopoietic Stem Cell
9%
Oligoastrocytoma
9%
Follicular Lymphoma
9%
Childhood Cancer
9%
STAT6 Protein
9%
Glioblastoma
9%
Minimal Residual Disease
9%
Neuroendocrine Carcinoma
9%
Transplantation
9%
Hematopoiesis
9%
Plant Gene
9%
Nucleoporin 98
9%
Uterine Cervix
9%
Atherosclerosis
9%
Breast Cancer
9%
Colorectal Cancer
9%
Ganglioglioma
9%
Human Immunodeficiency Virus
9%
Androgen Receptor
9%
Granular Cell
9%
Pediatrics Patient
9%
Plexiform Neurofibroma
9%
Desmoplastic Melanoma
9%
Brain Metastasis
9%
Differential Diagnosis
9%
Clustered Regularly Interspaced Short Palindromic Repeat
9%
Cas9
9%
Keyphrases
Next-generation Sequencing
46%
Formalin-fixed Paraffin-embedded Tissue
19%
Cell-free DNA (cfDNA)
18%
Isocitrate Dehydrogenase 1 (IDH1)
15%
Mutational Profiling
10%
Trunk
10%
Colorectal Cancer
10%
IDH-wildtype
10%
Driver mutations
10%
Renal Cell Carcinoma
10%
In(III)
10%
Clinical Validation
10%
Melanoma
10%
Metagenomic Next-generation Sequencing (mNGS)
10%
Gene Fusion
10%
Variant Allele Frequency
9%
Uterine Osteosarcoma
9%
Hematopoietic Cell Transplant
9%
Diffuse Glioma
9%
Serial Analysis
9%
Diagnostic Utility
9%
Artificial Intelligence
9%
Primary Lung Cancer
9%
1p36
9%
Clinical Laboratory
9%
Cancer Genomic Data
9%
1p/19q Codeletion
9%
Sequence Data
9%
Follicular Lymphoma
9%
Deletion Detection
9%
ErbB2
9%
Subclinical Atherosclerosis
9%
Minimal Residual Disease
9%
Primary Glioblastoma
9%
Chromophobe Renal Cell Carcinoma (chRCC)
9%
Human Epidermal Growth Factor Receptor 2 (HER2)
9%
People Living with HIV (PLHIV)
9%
Clonal Hematopoiesis
9%
Treatment Recommendations
9%
CREB1
9%
Diagnostic Platform
9%
Choriocarcinomatous Differentiation
9%
Cystic Renal Cell Carcinoma
9%
Co-mutation
9%
Therapeutic Implications
9%
Chimerism Testing
9%
Germ Cells
9%
Neuroblastoma
9%
BRAF mutation
9%
Androgen Receptor mutation
9%