Biochemistry, Genetics and Molecular Biology
Next Generation Sequencing
100%
BRCA1
91%
Genetic Screening
91%
Proband
82%
Genetic Divergence
70%
Promoter Region
63%
Germ Cell
59%
Germline
56%
Genome Sequencing
52%
Exome
51%
Array Comparative Genomic Hybridization
49%
Enhancer Region
49%
Missense
46%
Whole Genome Sequencing
40%
Autosomal Recessive Disorder
39%
Oncogene
35%
Tumor Gene
35%
Copy-Number Variation
33%
Epigenomics
33%
Penetrance
33%
Haploinsufficiency
33%
Programmed Cell Death
33%
Oxidative Phosphorylation
33%
Untranslated Region
33%
R-Loop
33%
Allele
29%
DNA Sequence
27%
Autosomal Dominant Inheritance
27%
Wild Type
27%
Genotype Phenotype Correlation
25%
Mental Retardation
24%
Fibroblast
23%
Albinism
23%
Transcription Factors
23%
RNA
23%
RNA Sequence
22%
Nuclear Gene
22%
Fibroblast
22%
16S Ribosomal RNA
22%
Exome Sequencing
22%
Regulatory Element
22%
Minigene
21%
Genetic Heterogeneity
21%
Small Nuclear RNA
21%
Genetic Mechanism
20%
Sanger Sequencing
20%
Methylation
20%
Gene Expression
20%
Binding Site
19%
Single-Nucleotide Polymorphism
19%
Medicine and Dentistry
Breast Cancer
49%
Diagnosis
44%
Diseases
37%
Genetic Screening
33%
Severe Acute Respiratory Syndrome Coronavirus 2
33%
In Silico
33%
BRCA1
31%
Tumor Gene
19%
Autosomal Recessive Disorder
18%
Clinical Feature
18%
Retina Disease
16%
Prevalence
16%
Eye Disease
16%
Homology Modeling
16%
Pathogenicity
16%
Growth Retardation
16%
Postnatal Growth
16%
Hypertelorism
16%
Anterior Chamber of Eyeball
16%
Eyebrow
16%
RNA Splicing
16%
Genitourinary System
16%
Cleft Lip Palate
16%
Absence
16%
Preschooler
16%
Ovarian Cancer
16%
Genetic Variability
16%
Genetic Heterogeneity
16%
BRCA2
10%
Rare Disease
8%
Gene Mutation
8%
DNA Sequence
8%
Visual Impairment
8%
Calcium Channel
8%
Cross-Validation
8%
Messenger RNA Precursor
8%
Amino Acid
8%
Congenital Stationary Night Blindness
8%
Orphan Disorder
8%
Ectopia Lentis
6%
Albinism
6%
Cataract
6%
Molecular Diagnosis
6%
