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UnknownBayesian Effect Size Ranking to Prioritise Genetic Risk Variants in Common Diseases for Follow-Up Studies.
Not available
S-EPMC11696485 | biostudies-literature
Genomicsena-DATASET-irgb_cnr-25-06-2013-12:35:10:789-8 - samples
1204 Sardinian males
EGAD00001000618 | EGA
GenomicsChromosome Y Philogeny in Sardinia
Genetic variation within the male specific portion of the Y chromosome (MSY) can clarify the origins of contemporary populations, but previous studies were hampered by partial genetic information. Population sequencing of 1,204 Sardinian males identified 11,763 MSY single nucleotide polymorphisms (S...
EGAS00001000532 | EGA
GenomicsSardinian Chromosome Y DAC
Data Access Committee EGAC00001000121
EGAC00001000121 | EGA
GenomicsGWAS results from Danjou et al, Nature Genetics 2015
GWAS results in epacts format for Danjou et al, Nature Genetics 2015
EGAD00010001722 | EGA
GenomicsGWAS Results from Danjou et al, Nature Genetics 2015
We report genome-wide association study results for the levels of A1, A2 and fetal hemoglobins, analyzed for the first time concurrently. Integrating high-density array genotyping and whole-genome sequencing in a large general population cohort from Sardinia, we detected 23 associations at 10 loci. ...
EGAS00001003645 | EGA
GenomicsAssociation studies using the Metabochip array - Samples analysed by the WTCCC (1958 British Birth Cohort (58BC), Hypertension cohort (HT), Type 2 Diabetes Cohort (T2D) and Coronary Artery Disease (CAD) cohort)
Genomewide association studies (GWAS) have proven a powerful hypothesis-free method to identify common disease-associated variants. Even quite large GWAS, however, have only at best identified moderate proportions of the genetic variants contributing to disease heritability. To provide cost-effectiv...
EGAS00000000115 | EGA
Genomicsena-DATASET-irgb_cnr-12-01-2017-10:08:18:724-1 - samples
List of SNPs, and their frequencies, extracted from a low pass whole genome sequencing of 3,514 individuals.
EGAD00001003141 | EGA
GenomicsWhole-genome low pass sequencing of 3,514 Sardinian individuals
The dataset includes the VCF files with the list of variants, and their frequency, found in 3,514 Sardinian individuals recruited from the SardiNIA longitudinal study (N=2090) and from a case-control study of autoimmune diseases in Sardinia (N=1424).
EGAS00001002212 | EGA
GenomicsSardiNIA population frequency DAC
Data Access Committee EGAC00001000590
EGAC00001000590 | EGA
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