Keyphrases
Neurological Disorders
100%
Community Genomics
100%
Genomic Studies
100%
Oman
100%
Autosomal Recessive
66%
University College London
50%
St. George
50%
Ministry of Health
33%
Genetic Disorders
33%
DNA Sequencer
33%
Sultan Qaboos University
33%
Gene Sequencing
16%
Biological Research
16%
DNA Isolation
16%
Roche 454 Sequencing
16%
Disease Gene Prioritization
16%
Gene mutation
16%
Imaging Facility
16%
Expression Study
16%
Sequencing Platforms
16%
Parallel Development
16%
ChIP-seq Analysis
16%
Rare Diseases
16%
Group Members
16%
Existing Techniques
16%
Genetic Services
16%
Work Plan
16%
Disease Gene Discovery
16%
Type of Marriage
16%
Disease Gene Identification
16%
Causative Gene
16%
Clinical Expertise
16%
Molecular Study
16%
Primary Health Care System
16%
Affymetrix GeneChip
16%
Biomics
16%
SNP chip
16%
Collaborative Access
16%
Electron Microscopy
16%
Illumina Microarray
16%
Mutation Identification
16%
Prevelance
16%
Confocal Microscope
16%
Genome Sequence Analysis
16%
Strategic Projects
16%
Next-generation Sequencing
16%
Consanguineous Marriage
16%
Higher Education
16%
Genetic Disease
16%
Omani
16%
Massively Parallel Sequencing
16%
Research Fund
16%
Principal Investigator
16%
Medical Doctors
16%
Laboratory Facility
16%
Microarray
16%
Molecular Biology Laboratory
16%
Research-based
16%
Genetic Testing
16%
Innovative Technique
16%
Informed Consent
16%
INIS
oman
100%
communities
100%
diseases
100%
genes
85%
universities
71%
genetics
71%
availability
28%
dna sequencers
28%
pipelines
28%
populations
28%
state government
28%
molecular biology
14%
education
14%
control
14%
guidelines
14%
data
14%
microscopes
14%
animals
14%
phenotype
14%
testing
14%
laboratories
14%
mutations
14%
equipment
14%
documentation
14%
electron microscopy
14%
gene mutations
14%
dna
14%
range
14%
Medicine and Dentistry
Diseases
100%
Neurologic Disease
100%
Genetic Disorder
60%
Clinician
40%
Next Generation Sequencing
40%
Autosomal Recessive Inheritance
40%
Autosomal Recessive Disorder
40%
Confocal Microscopy
20%
Primary Health Care
20%
Informed Consent
20%
Genetic Screening
20%
Single Nucleotide Polymorphism
20%
Rare Disease
20%
Disease Gene Identification
20%
DNA Isolation
20%
Linkage Analysis
20%
Physician
20%
Gene Discovery
20%
Gene Mutation
20%
Base
20%
Electron Microscopy
20%