BLUEPRINT September 2016, ChIPmentation for CD38-negative naive B cell from cord blood, on Genome GRCh38

ChIPmentation data for 1 sample(s) for CD38-negative naive B cell from cord blood, on Genome GRCh38. 5 run(s), 3 experiment(s), 3 alignment(s). Part of BLUEPRINT (September 2016).

21/11/2016
1 sample
DAC: EGAC00001000135
Technology: NextSeq 500

Access Policy1 Study Files

Metadata

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Access to the sequence and alignment and genotype level data produced by the Blueprint Consortium is controlled by the Blueprint Data Access Committee (DAC). Access to data will be granted to qualified investigators for appropriate use. Please email blueprint-dac@ebi.ac.uk to request data access.

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
EGAS00001000326	BLUEPRINT ChIP-seq data for cells in the haematopoietic lineages, from adult and cord blood samples.	Epigenetics

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
EGAF00001227976	fastq.gz	375.8 MB
EGAF00001227977	fastq.gz	393.0 MB
EGAF00001227978	fastq.gz	413.9 MB
EGAF00001227979	fastq.gz	448.1 MB
EGAF00001228050	fastq.gz	82.9 MB
EGAF00001228051	fastq.gz	87.8 MB
EGAF00001228052	fastq.gz	92.8 MB
EGAF00001228053	fastq.gz	104.7 MB
EGAF00001228096	fastq.gz	197.3 MB
EGAF00001228097	fastq.gz	205.0 MB
EGAF00001398524	bam	555.7 MB
EGAF00001398571	bam	842.0 MB
EGAF00001398596	bam	867.1 MB
13 Files (4.7 GB)