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Genome Information for Homo sapiens
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 TwinsUK and ALSPAC
cohorts (at 6x sequence coverage), and the exome sequence (protein-coding regions and
related conserved sequence) of 6000 samples selected for extreme phenotypes. Our studies
will focus primarily on cardiovascular-related quantitative traits, obesity and related
metabolic traits, neurodevelopmental disorders and a limited number of extreme clinical
phenotypes that will provide proof-of-concept for future familial trait sequencing.
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 TwinsUK and ALSPAC
cohorts (at 6x sequence coverage), and the exome sequence (protein-coding regions and
related conserved sequence) of 6000 samples selected for extreme phenotypes. Our studies
will focus primarily on cardiovascular-related quantitative traits, obesity and related
metabolic traits, neurodevelopmental disorders and a limited number of extreme clinical
phenotypes that will provide proof-of-concept for future familial trait sequencing. We
will directly analyse quantitative traits in the cohorts and the selected traits in the
extreme samples, and also use imputation down to 0.1% allele frequency to extend the
analyses to further sample sets with genome wide genotype data. In each case we will
investigate indels and larger structural variants as well as SNPs, and use statistical
methods that combine rare variants in a locus or pathway as well as single-variant
approaches. The TwinsUK samples will be part of the cohort study and will undergo whole
genome sequencing. For further information with regard to this cohort please contact
Brent Richards (
[email protected]) or Nicole Soranzo
(
[email protected]).
Less...Accession | PRJEB6040 |
Type | Umbrella project |
Submission | Registration date: 5-Apr-2014 European Bioinformatics Institute |
This project encompasses the following 2 sub-projects:
Project Type | Number of Projects |
Other | 2 |
BioProject accession | Organism | Title |
---|
PRJEB7217 | Homo sapiens | UK10K Avon Longitudinal Study of Parents and Children (ALSPAC) Variants (European Bioinformatics Institute) | PRJEB7218 | Homo sapiens | UK10K The Department of Twin Research and Genetic Epidemiology (TwinsUK) Variants (European Bioinformatics Institute) |
|