Associations between APOE and cognitive ability in Generation Scotland.
This DAC controls 4 datasets:
|EGAD00001000181||UK10K_OBESITY_SCOOP REL-2012-01-13||Illumina HiSeq 2000||212|
|EGAD00001000318||UK10K_NEURO_FSZ REL-2012-11-27||Illumina HiSeq 2000||119|
|EGAD00001000819||We are aiming to investigate repair of a double strand break (DSB) within the genome in the presence and absence of the BLOOM protein. Zinc Finger Nucleases introduce DSBs at specified loci within the genome. Using sequencing we will assess the size of the deletion following repair. Protocol 1. Transfect normal and BLOOM deficient human iPS cells with ZFNs, using AMXA 2. Harvest cells after 5 days 3. Perform column extraction of DNA 4. PCR-amplify the ZFN region 5. Sequence and analyse repair of the DSB This data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute (including details of any publication moratoria), please see http://www.sanger.ac.uk/datasharing/||Illumina MiSeq||6|
|EGAD00010000738||Generation Scotland APOE data||18336|