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GenomicsWhole-Genome Sequencing of 128 Ashkenazi Jewish individuals
We sequenced 128 individuals of Ashkenazi Jewish ancestry. All individuals were controls in other studies: (1) Longevity (Gil Atzmon's lab; Albert Einstein College of Medicine), n=74. (2) Parkinson's disease (Lorraine Clark's lab; Columbia University Medical Center), n=54. Whole-genome, high-cover...
EGAS00001000664 | EGA
Genomicsena-DATASET-TAGC-18-03-2014-13:20:29:283-320 - samples
Whole genome, high coverage, sequencing of 128 Ashkenazi Jewish controls
EGAD00001000781 | EGA
GenomicsThe Ashkenazi Genome Consortium Data Access Committee
Data Access Committee EGAC00001000151
EGAC00001000151 | EGA
GenomicsCopy Number Variation in Congenital Kidney Malformations

We report a study of large rare, copy number variants (CNVs) in 192 patients with renal hypodysplasia (RHD). Congenital malformations of the kidney and urinary tract are present in 3 to 7 per 1,000 births, accounting for 16% of birth defects. These malformations account for 40-50% of pediatric an...

phs000565.v1.p1 | EGA
UnknownSame data, different analysts: variation in effect sizes due to analytical decisions in ecology and evolutionary biology.
Not available
S-EPMC11804095 | biostudies-literature
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