WARNING: the interactive features of this website use CSS3, which your browser does not support. To use the full features of this website, please update your browser.
157,314 bulk items are available, covering 157,314 participants.
There are 1 distinct values.
Mean = 1
Std.dev = 0
Estimation of human contamination in whole genome sequencing data, generated using ReadHaps software (https://github.com/DecodeGenetics/read_haps). This is provided for all samples sequenced by deCODE, and for any main phase samples sequenced by Wellcome Sanger Institute with a calculated sample contamination over 1% using Freemix VerifyBamID.
This data is currently restricted and is anticipated for public release in late 2023.
0 Related Data-Fields
There are no related data-fields
There are no matching Resources
Enabling scientific discoveries that improve human health