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GenomicsSearch for new loci and low-frequency variants influencing glioma risk by exome-array analysis
To identify protein altering variants (PAVs) for glioma we analysed Illumina HumanExome BeadChip exome array data on 1,882 glioma cases and 8,079 controls from three independent European populations. In addition to single variant tests we incorporated information on the predicted functional conseque...
EGAS00001001258 | EGA
Genomicsena-DATASET-ICR-PTGT-15-10-2018-17:54:40:362-3 - samples
BAM files of individuals from the 1958BC aligned to hg17
EGAD00001004396 | EGA
GenomicsICR MOPOPGEN UK exome control series
ICR MOPOPGEN UK exome control series
EGAS00001001667 | EGA
GenomicsGlioma_Exome_FRE_CASES - samples
French glioma case germline genotypes using Illumina HumanExome-12v1_A array
EGAD00010000758 | EGA
GenomicsGlioma_Exome_UK_CASES - samples
UK glioma case germline genotypes using Illumina HumanExome-12v1_A array
EGAD00010000754 | EGA
GenomicsGlioma_Exome_FRE_CONTROLS - samples
French glioma control germline genotypes using Illumina HumanExome-12v1_A array
EGAD00010000756 | EGA
GenomicsGlioma_Exome_GER_CASES - samples
German glioma case germline genotypes using Illumina HumanExome-12v1_A array
EGAD00010000752 | EGA
GenomicsGlioma_Exome_GER_CONTROLS - samples
German glioma control germline genotypes using Illumina HumanExome-12v1_A array
EGAD00010000750 | EGA
GenomicsGlioma exome array DAC
Data Access Committee EGAC00001000345
EGAC00001000345 | EGA
GenomicsGlioma GWAS summary statistics
Meta-analysis association statistics from case-control analysis (includes imputed SNPs)
EGAD00010001657 | EGA
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