BLUEPRINT release August 2015, RNA-Seq for neutrophilic myelocyte, on genome GRCh38

RNA-Seq data for 3 neutrophilic myelocyte sample(s). 3 run(s), 3 experiment(s), 3 alignment(s) on human genome GRCh38. Part of BLUEPRINT release August 2015. Analysis documentation available at http://ftp.ebi.ac.uk/pub/databases/blueprint/releases/20150820/homo_sapiens/README_rnaseq_analysis_crg_20150820

17/08/2016
3 samples
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
	BLUEPRINT RNA-seq data for common cells in the haematopoietic lineages, from adult and cord blood samples.	Transcriptome Analysis

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
EGAF00000694361	fastq.gz	9.1 GB
EGAF00000694362	fastq.gz	9.1 GB
EGAF00000694363	fastq.gz	8.7 GB
EGAF00000694364	fastq.gz	8.8 GB
EGAF00000694365	fastq.gz	8.9 GB
EGAF00000694366	fastq.gz	8.9 GB
EGAF00000866526	bam	20.5 GB
EGAF00000866651	bam	20.3 GB
EGAF00000867018	bam	21.1 GB
9 Files (115.4 GB)