Analysis of Czech genomes for terranostik (Q20003): Difference between revisions

From EU Knowledge Graph
Jump to navigation Jump to search
(‎Removed claim: summary (P836): The objective of the project is the creation of a national reference database — the tool to group the genetic variability of the Czech population. A sample of 1000 healthy people will undergo a sequential analysis of the data obtained and a sequence of analysis of the data obtained. The identified variants, together with their frequency in the population, will be included in the database. These data are necessary for the correct interpretation...)
(‎Created claim: summary (P836): The aim of the project is to create a national reference database – a tool that will simulate the genetic variability of the Czech population. On a sample of 1000 healthy populations, all-genomal sequencing will be performed and subsequently analysed the data obtained. The identified variants, along with their frequency in the population, will be inserted into the database. These data are necessary for the correct interpretation of diagnostic ge...)
Property / summary
 
The aim of the project is to create a national reference database – a tool that will simulate the genetic variability of the Czech population. On a sample of 1000 healthy populations, all-genomal sequencing will be performed and subsequently analysed the data obtained. The identified variants, along with their frequency in the population, will be inserted into the database. These data are necessary for the correct interpretation of diagnostic genetic tests. a. (English)
Property / summary: The aim of the project is to create a national reference database – a tool that will simulate the genetic variability of the Czech population. On a sample of 1000 healthy populations, all-genomal sequencing will be performed and subsequently analysed the data obtained. The identified variants, along with their frequency in the population, will be inserted into the database. These data are necessary for the correct interpretation of diagnostic genetic tests. a. (English) / rank
 
Normal rank
Property / summary: The aim of the project is to create a national reference database – a tool that will simulate the genetic variability of the Czech population. On a sample of 1000 healthy populations, all-genomal sequencing will be performed and subsequently analysed the data obtained. The identified variants, along with their frequency in the population, will be inserted into the database. These data are necessary for the correct interpretation of diagnostic genetic tests. a. (English) / qualifier
 
point in time: 22 October 2020
Timestamp+2020-10-22T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

Revision as of 17:35, 22 October 2020

Project in Czech Republic financed by DG Regio
Language Label Description Also known as
English
Analysis of Czech genomes for terranostik
Project in Czech Republic financed by DG Regio

    Statements

    0 references
    71,921,256.5 Czech koruna
    0 references
    2,876,850.26 Euro
    10 January 2020
    0 references
    94,757,913.7 Czech koruna
    0 references
    3,790,316.55 Euro
    10 January 2020
    0 references
    75.9 percent
    0 references
    1 January 2019
    0 references
    31 December 2022
    0 references
    Masarykova univerzita
    0 references
    0 references

    49°12'8.64"N, 16°36'28.44"E
    0 references

    49°11'55.68"N, 16°36'7.06"E
    0 references
    60200
    0 references
    Cílem projektu je vytvoření národní referenční databáze - nástroje, který bude napovat genetickou variabilitu české populace. Na vzorku 1000 zdravých obyvatel bude provedeno celogenomové sekvenování a nasledně analýza získaných dat. Identifikované varianty budou spolu s jejich frekvencí v populaci vloženy do databáze. Tato data jsou nezbytná pro správnou interpretaci diagnostickách genetickách testů. a. (Czech)
    0 references
    The aim of the project is to create a national reference database – a tool that will simulate the genetic variability of the Czech population. On a sample of 1000 healthy populations, all-genomal sequencing will be performed and subsequently analysed the data obtained. The identified variants, along with their frequency in the population, will be inserted into the database. These data are necessary for the correct interpretation of diagnostic genetic tests. a. (English)
    22 October 2020
    0 references

    Identifiers

    CZ.02.1.01/0.0/0.0/16_026/0008448
    0 references