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Investigating low frequency variants in CAD/MI cases, controls and pedigrees using whole exome sequencing and custom pulldowns

The Cardiogenics re-sequencing study will consist of three parts: Eight pools of 25 individuals will be sequenced using a Nimblegen hybrid-capture solution specific to miRNA sequences, 80 pools of 25 individuals will be sequenced using a custom Agilent SureSelect array covering genes associated with coronary artery disease (CAD) and myocardial infarction (MI), 10 individuals from families with a history of CAD/MI will be exome sequenced using the Sanger exome array. The experiment will use the early onset patients from the German MI cohort and the UK BHF CAD/MI cohort both of which have strong family history. For controls we will consider individuals from the UKBS and KORA cohorts.

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Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.

Study ID Study Title Study Type
EGAS00001000043 Other

This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.

ID File Type Size Located in
EGAF00000078915 bam 13.5 GB
EGAF00000078916 bam 12.8 GB
EGAF00000078917 bam 12.9 GB
EGAF00000078918 bam 13.3 GB
EGAF00000078919 bam 13.3 GB
EGAF00000078920 bam 13.4 GB
EGAF00000078921 bam 13.6 GB
EGAF00000078922 bam 17.3 GB
EGAF00000078923 bam 16.1 GB
EGAF00000078924 bam 17.1 GB
EGAF00000078925 bam 17.0 GB
EGAF00000081183 bam 14.4 GB
12 Files (174.7 GB)