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NIHR BioResource Rare Diseases WGS project - Ehler-Danlos (ED) and ED-like Syndromes (EDS) Rare Disease domain

Short read whole genome sequencing (WGS) CRAM files for the NIHR BioResource Rare Diseases WGS project – Participants from the Ehler-Danlos (ED) and ED-like Syndromes (EDS) Rare Disease domain.

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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
EGAS00001001012 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
EGAF00001194634 cram 38.8 GB
EGAF00001215617 cram 38.2 GB
EGAF00001237990 cram 33.8 GB
EGAF00001237998 cram 36.6 GB
EGAF00001238022 cram 33.6 GB
EGAF00001238025 cram 33.1 GB
EGAF00001238045 cram 39.4 GB
EGAF00001238051 cram 38.7 GB
EGAF00001238060 cram 33.7 GB
EGAF00001238063 cram 34.5 GB
EGAF00001238067 cram 33.4 GB
EGAF00001238081 cram 30.8 GB
EGAF00001299599 cram 34.2 GB
EGAF00001299620 cram 35.5 GB
EGAF00001299624 cram 34.8 GB
EGAF00001396666 cram 39.7 GB
EGAF00001777461 cram 46.3 GB
EGAF00001777464 cram 44.7 GB
EGAF00001777465 cram 44.7 GB
EGAF00001777467 cram 44.2 GB
EGAF00001777478 cram 44.7 GB
EGAF00001777480 cram 44.3 GB
EGAF00002239614 cram 36.4 GB
23 Files (874.1 GB)