Genomics

Dataset Information

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UK10K The Department of Twin Research and Genetic Epidemiology (TwinsUK) Variants


ABSTRACT: 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).

INSTRUMENT(S): Illumina HiSeq 2000

ORGANISM(S): Homo Sapiens

SUBMITTER: Wellcome Trust Sanger Institute 

PROVIDER: PRJEB7218 | EVA | 2014-10-20

REPOSITORIES: EVA

Dataset's files

Source:
Action DRS
TWINSUK.beagle.anno.csq.shapeit.20131101.sites.vcf.gz Vcf
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