BLUEPRINT September 2016, ChIPmentation for naive B cell from tonsil, on Genome GRCh38

ChIPmentation data for 1 sample(s) for naive B cell from tonsil, on Genome GRCh38. 1 run(s), 1 experiment(s), 1 alignment(s). Part of BLUEPRINT (September 2016).

21/11/2016
1 sample
DAC: EGAC00001000135
Technology: Illumina HiSeq 2000

Access Policy1 Study Files

Metadata

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Blueprint Data Access Policy

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
EGAF00001344827	fastq.gz	3.9 GB
EGAF00001344828	fastq.gz	2.3 GB
EGAF00001398572	bam	5.5 GB
3 Files (11.7 GB)