Assesment of Multiomics Profiles in Health and Disease.
Condition(s) studied
Investigational drug(s) / intervention(s)
Blood sample analysis: Nucleic acids sequencing, presence of proteins and metabolites.
Health status: Health status will be examined by a physician and subject will complete a health status questionnaire.
Race and ethnicity: Subject will complete race and ethnicity questionnaire to make sure subjects are from the Czech population.
Study summary
This study will determine reference genomic, transcriptomic, proteomic and metabolomic profiles in Czech population and will evaluate its correlation with the disease phenotype.
Eligibility
Primary outcome measure(s)
- Whole Genome (Exom) Sequencing of the Healthy Volunteers - establishment of the HEALTHY VOLUNTEER REFERENCE GENOME (min. 1000 individuals) — 72 months
Establishment of the Healthy Volunteers Whole Genome (Exom) Reference Database typical for the population of the Czech Republic/Central Europe. - Whole Genome (Exom) Sequencing of the patient groups with different diseases and their comparison to the HEALTHY VOLUNTEER REFERENCE GENOME — 72 months
Whole Genome (Exom) Sequencing of the patient populations presenting various diseases. Based on the comparison with the HEALTHY VOLUNTEER REFERENCE GENOME - determination of various genetic polymorphisms (single nucleotide polymorphisms, insertions, deletions, inversions, copy-number variations etc.) and giving these into correlation with disease phenotypes.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| University Hospital Olomouc | Olomouc | Czechia | Recruiting |
More The Institute of Molecular and Translational Medicine, Czech Republic trials in Czechia
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04427163 on ClinicalTrials.gov ↗ ← All trials in Czechia