Biochemistry, Genetics and Molecular Biology
Next Generation Sequencing
100%
Single-Nucleotide Polymorphism
46%
Trisomy
42%
Fusion Gene
26%
Prevalence
26%
Genetics
26%
Exon
25%
Optical Genome Mapping
24%
RNA
22%
ITPR1
21%
Droplet Digital Polymerase Chain Reaction
21%
Plasmid
21%
Sanger Sequencing
21%
Gene Frequency
21%
Newborn Screening
21%
Screening Test
21%
Dilution
21%
RNA Sequence
21%
Cas9
21%
Genetic Screening
21%
RFC1
21%
Exome Sequencing
18%
Myeloid
15%
Indel
14%
Metabolic Disorder
14%
Whole Genome Sequencing
14%
Gene Fusion
13%
Karyotyping
12%
PPP2R2B
10%
Genotyping
10%
Reverse Transcription Polymerase Chain Reaction
7%
Promoter Region
7%
Gene Locus
7%
Fluorescence in Situ Hybridization
7%
Dried Blood Spot
7%
Aneuploidy
5%
RNA Sequencing
5%
Reverse Transcription Polymerase Chain Reaction
5%
Deep Sequencing
5%
FGF14
5%
Coding Region
5%
Alpha 1-Antitrypsin
5%
Data Processing
5%
Medline
5%
Keyphrases
Variation Reduction
21%
NGS Data
21%
Sanger Sequencing
21%
Targeted NGS
21%
Copy number Variation Detection
21%
Clinical Diagnostics
21%
Gene Doping Detection
21%
Intronic Repeat Expansion
21%
Variants of Uncertain Significance
21%
Next-generation Sequencing
21%
Variant Classification
21%
Newborn Screening
21%
Classification Strategy
21%
Dutch
21%
Leukemia Classification
14%
ITPR1
9%
Whole Exome Sequencing
8%
Inherited Metabolic Diseases
8%
Filtering Strategy
8%
Metagenomic Next-generation Sequencing (mNGS)
8%
Whole Genome Sequencing
8%
True-false
8%
Fair Competition
7%
Pan-cancer
7%
Variant Patterns
7%
Variant Impact
5%
VCF Files
5%
SnpEff
5%
ExAC Database
5%
CADD Score
5%
Non-invasive Prenatal Test
5%
Deleteriousness
5%
Chromosomal Origin
5%
Leukemia Screening
5%
Medicine and Dentistry
Next Generation Sequencing
42%
Trisomy
31%
Clinician
21%
Neoplasm
21%
Minimal Residual Disease
21%
Leukemia
21%
Fusion Gene
21%
Droplet Digital Polymerase Chain Reaction
21%
Cell Line
16%
Counseling
10%
Decision Making
10%
Gene Fusion
8%
Sensitivity and Specificity
5%
Maternal Plasma
5%
Cell-Free DNA
5%
Aneuploidy
5%
