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ugli [2025/12/19 15:17] – sylviaugli [2025/12/19 16:05] (current) – sylvia
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 ===== UGLI2+3 - Affymetrix ===== ===== UGLI2+3 - Affymetrix =====
 Important to note: **UGLI3 currently has a publication restriction**. the UGLI-consortium is currently preparing their manuscript describing the dataset and its primary analyses. Other manuscripts using UGLI3 data may not be submitted **before 31 December 2026**. Important to note: **UGLI3 currently has a publication restriction**. the UGLI-consortium is currently preparing their manuscript describing the dataset and its primary analyses. Other manuscripts using UGLI3 data may not be submitted **before 31 December 2026**.
-\\ + 
-As of december 2025, data of 60,157 genotyped participants has been made available. Samples in this release, called UGLI2+3, were genotyped using the FinnGen Thermo Fisher Axiom® custom array. The sample includes the previously genotyped participants from UGLI2 (see above). The QC and imputation was done on the combined dataset of UGLI2 and UGLI3.+As of december 2025, data of 60,157 genotyped participants have been made available. Samples in this release, called UGLI2+3, were genotyped using the FinnGen Thermo Fisher Axiom® custom array. The sample includes the previously genotyped participants from UGLI2 (see above). The QC and imputation was done on the combined dataset of UGLI2 and UGLI3.
  
 63,553 participants were selected for UGLI 2+3 release and assessed using the pre mentioned array. All genotypes were included for QC screening, but the QC focussed on the the autosomes and chromosomes X for which there are N=615,682 and 22,346 markers available, respectively. A final set of 60,157 samples and 476,693 markers on autosomal and X chromosomes passed the QC steps described in the quality check rapport. 63,553 participants were selected for UGLI 2+3 release and assessed using the pre mentioned array. All genotypes were included for QC screening, but the QC focussed on the the autosomes and chromosomes X for which there are N=615,682 and 22,346 markers available, respectively. A final set of 60,157 samples and 476,693 markers on autosomal and X chromosomes passed the QC steps described in the quality check rapport.
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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.haplotypereference-consortium.org) panel. +Sanger imputation service using the Haplotype Reference Consortium (http://www.haplotype-reference-consortium.org) panel. 
 Method: See QC report Method: See QC report
  
ugli.1766157474.txt.gz · Last modified: by sylvia