Keyphrases
Copy number Variation
100%
Whole Exome Sequencing
100%
Germ Cells
100%
Somatic Aberrations
100%
Tumor-normal
100%
Germline Variants
100%
Rare Cancer
100%
Rare Tumors
100%
Oncogene
66%
Tumor Suppressor Gene
66%
Small Indel
66%
Next-generation Sequencing
33%
Cancer Genes
33%
Cell Fate
33%
Cancer Patients
33%
Biologically Relevant
33%
Tumor
33%
Tumor Subtype
33%
Common Cancers
33%
Clinical Significance
33%
Gene Pathway
33%
Relevant Genes
33%
Genetic mutation
33%
Cancer Cases
33%
Normal Pair
33%
Somatic Variants
33%
Single nucleotide Variant
33%
Novel Variants
33%
Hippo
33%
Patient with Tumor
33%
Pathway mutation
33%
Double Hit
33%
Germline Pathogenic Variant
33%
Somatic Single nucleotide Variants
33%
Biochemistry, Genetics and Molecular Biology
Exome Sequencing
100%
Germ Cell
100%
Germline
100%
Oncogene
50%
Tumor Suppressor Gene
33%
Indel
33%
Single-Nucleotide Polymorphism
33%
Next Generation Sequencing
16%
Allele
16%
Notch
16%
Cell Fate
16%
Tumor Gene
16%