See
Genome Information for Homo sapiens
Navigate Up
This project is a component of the
UK10KNavigate Across
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 TwinsUK study. For further information with regard to this cohort please contact Brent Richards (brent.richards@kcl.ac.uk) or Nicole Soranzo (ns6@sanger.ac.uk).
Less...| Accession | PRJEB7218 |
| 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 |
Project Data:
No public data is linked to this project. Any recently released data that cites this project will be linked to it within a few days.