PRDM13 exome sequencing set
Exome sequencing study on 4 individuals from a pedigree with CHH and cerebellar hypoplasia.
- 8 samples
- DAC: EGAC00001002454
- Technology: Illumina HiSeq 2500
See our policy for how to access data.
Check that the user will be using the data within terms of consent, by asking them to sign up to the terms within the DAA Check for an Institutional email address for the requestor * Look for evidence of the requestor being “appropriately qualified/bona fide” for use of the data e.g., PubMed search, Research Gate, LinkedIn etc. Check the affiliated organisation is real and that they are still working there
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 |
---|---|---|
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 | |
---|---|---|---|---|
EGAF00005740419 | 1639404840176 | 4.2 GB | ||
EGAF00005740420 | 1639405080541 | 5.1 GB | ||
EGAF00005740421 | 1639404900199 | 5.2 GB | ||
EGAF00005740422 | 1639405021120 | 4.5 GB | ||
EGAF00005740423 | 1639404960177 | 5.8 GB | ||
EGAF00005740424 | 1639405260202 | 5.1 GB | ||
EGAF00005740425 | 1639405260202 | 4.6 GB | ||
EGAF00005740426 | 1639405200189 | 4.8 GB | ||
8 Files (39.3 GB) |