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The UK10K project proposes a series of complementary genetic approaches to find new low-frequency/rare variants contributing to disease phenotypes.
More...The UK10K project proposes a series of complementary genetic approaches to find new low-frequency/rare variants contributing to disease phenotypes. These will be based on obtaining the genome-wide sequence of 4000 samples from the Department of Twin Research and Genetic Epidemiology (TwinsUK) and Avon Longitudinal Study of Parents and Children (ALSPAC) cohorts (at 6x sequence coverage), and the exome sequence (protein-coding regions and related conserved sequence) of 6000 samples selected for extreme phenotypes. This project describes the variants identified from the ALSPAC study. For further information with regard to this cohort please contact Brent Richards (
[email protected]) or Nicole Soranzo (
[email protected]).
Less...| Accession | PRJEB7217 |
| Scope | Monoisolate |
| Organism | Homo sapiens[Taxonomy ID: 9606] Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens |
| Submission | Registration date: 10-Sep-2014
European Bioinformatics Institute |
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