تخطي إلى التنقل الرئيسي
تخطي إلى البحث
تخطي إلى المحتوى الرئيسي
الصفحة الرئيسية
المساعدة والأسئلة الشائعة
English
العربية
الصفحة الرئيسية
الوحدات البحثية
الملفات الشخصية
نتاج البحث
المشاريع
المعدات
أنشطة
مجموعات البيانات
الصحافة / وسائل الإعلام
الجوائز
التأثيرات
الدورات التدريبية
البحث حسب الخبرة أو الاسم أو الانتماء
A community genomic study of inherited neurological disorders in Oman
Al Shehi, Aisha Hassan
(PI)
Biology
المشروع
:
بحوث المنح الداخلية
معاينة
بصمة
بصمة
استكشف موضوعات البحث التي تناولها هذا المشروع. يتم إنشاء هذه الملصقات بناءً على الجوائز/المنح الأساسية. فهما يشكلان معًا بصمة فريدة.
فرز حسب
الوزن
أبجديًا
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%