DNMT3A microcephalic primordial dwarfism RRBS data

RRBS sequence data from one control and one patient with de novo DNMT3A mutations resulting in microcephalic primordial dwarfism.

2 samples
DAC: EGAC00001000393
Technology: NextSeq 550

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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
EGAS00001003232	Gain of function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions	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
EGAF00002191754	fq.gz	960.7 MB
EGAF00002191755	fq.gz	994.1 MB
EGAF00002191756	fq.gz	3.8 GB
EGAF00002191757	fq.gz	4.1 GB
4 Files (9.9 GB)