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ugli [2026/06/04 09:33] – [Imputation] sylviaugli [2026/06/04 09:33] (current) – [Imputation] sylvia
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 ====Imputation==== ====Imputation====
-A final set of 28,149 samples and 460,136 markers on autosomal and X chromosomes passing all QC steps described above were used for genetic imputation. Genetic imputation was done through the Sanger imputation service using the Haplotype Reference Consortium (http://www.haplotype-reference-consortium.org) panel.+A final set of 28,149 samples and 460,136 markers on autosomal and X chromosomes passing all QC steps described above were used for genetic imputation. Genetic imputation was done through the Sanger imputation service using the Haplotype Reference Consortium (https://www.sanger.ac.uk/collaboration/haplotype-reference-consortium/) panel.
  
 ====SNP array intensity files==== ====SNP array intensity files====
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 ====Imputation==== ====Imputation====
 A final set of 60,157 samples and 476,693 markers on autosomal and X chromosomes passing all QC steps described in the QC rapport and were used for genetic phasing and imputation. Genetic imputation was done through the  A final set of 60,157 samples and 476,693 markers on autosomal and X chromosomes passing all QC steps described in the QC rapport and were used for genetic phasing and imputation. Genetic imputation was done through the 
-Sanger imputation service using the Haplotype Reference Consortium (http://www.haplotype-reference-consortium.org) panel. +Sanger imputation service using the Haplotype Reference Consortium (https://www.sanger.ac.uk/collaboration/haplotype-reference-consortium/) panel. 
 Method: See QC report Method: See QC report
  
ugli.1780565580.txt.gz · Last modified: by sylvia