Dataset

Menselijk Genoom Data (1+MG) - SNPs matrix

Gegevens van volledige genoomsequencing van 100 bloedmonsters die zijn afgenomen bij een referentiecohort dat representatief is voor de algemene Belgische bevolking. Een matrix met Single Nucleotide Variants (SNV’s) die zijn geïdentificeerd in een steekproef van 100 BELHES-deelnemers. Het bestand is een CSV-bestand met één regel per monster (gepseudonimiseerde ID) en één kolom per variant. De kolomkoppen zijn chr:positie. De gebruikte referentiegenoomversie was GRCh38.

Overzicht

Trefwoorden
genetic population-based Whole-genome
Talen
en
Health Categories
Human genetic, epigenomic and genomic data
Population Coverage
The sample size of the current study is determined by the number of BELHES participants who have signed an informed consent form for the collection of a blood sample and subsequent DNA analysis, and with their blood sample stored in Sciensano’s biobank.
Purposes
  • The primary objective of the project is to obtain DNA sequencing results from residual blood samples that have been collected from a reference cohort reflecting the general Belgian population

Provenance
  • The blood samples, together with their lab ID, have been sent to KULeuven for sequencing and the generated sequencing data are stored at the secured internal network server at Sciensano

Temporal Information

Temporal Coverage
Begin
Einde
Metadata Dates
Issued:
Modified:

Spatial Information

Geographic Coverage
  • BE
NUTS Codes
http://data.europa.eu/nuts/code/BE

Distributions & Resources

Belgian Health Data Agency | Request Form

https://www.hda.belgium.be/en/data_request

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Publication Info
License cc-zero1.0
Standards & Languages
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Conforms To
Distribution Profile
Human Genomics Data (1+MG) - SNPs matrix | Data dictionary

https://raw.githubusercontent.com/sciensanogit/SciensanoDataPortal_distributions/refs/heads/main/datasets/1%252BMG-SNP/datadic.ttl

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Beschrijving

Data dictionary (long format). A matrix containing Single Nucleotide Variants (SNVs) identified in a sample of 100 BELHES participants. The file is a CSV file with one line per sample (pseudonymised ID) and one column per variant. Column headers are chr:position. Reference genome version used was GRCh38.

Publication Info
License cc-zero1.0
Technical Details
MIME Type http://www.iana.org/assignments/media-types/text/turtle
Standards & Languages
Talen en
Conforms To
Sample Profile
Direct Links
Download URL Downloaden
Human Genomics Data (1+MG) - SNPs matrix | Illustrative structure (mock)

https://github.com/sciensanogit/SciensanoDataPortal_distributions/blob/main/datasets/1%252BMG-SNP/illustrativestructure-snpmatrix.png

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Beschrijving

Illustrative structure of a SNP matrix (mock).

Publication Info
License cc-zero1.0
Standards & Languages
Talen en
Conforms To
Sample Profile
Direct Links
Download URL Downloaden