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Series GSE136703 Query DataSets for GSE136703
Status Public on Feb 11, 2020
Title Assessing the ability of various genomic features to prioritize causal non-coding variants associated with diseases and traits
Organisms Homo sapiens; unidentified plasmid
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Other
Summary This SuperSeries is composed of the SubSeries listed below.
 
Overall design Refer to individual Series
 
Citation(s) 32144282
Submission date Aug 30, 2019
Last update date Apr 01, 2020
Contact name Carl G de Boer
Organization name The Broad Institute
Lab Aviv Regev
Street address 415 Main St
City Cambridge
State/province MA
ZIP/Postal code 02139
Country USA
 
Platforms (5)
GPL15520 Illumina MiSeq (Homo sapiens)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
GPL18573 Illumina NextSeq 500 (Homo sapiens)
Samples (210)
GSM4055235 BJAB_0
GSM4055236 BJAB_1
GSM4055237 BJAB_4
This SuperSeries is composed of the following SubSeries:
GSE136686 Assessing the ability of various genomic features to prioritize causal non-coding variants associated with diseases and traits [ATAC-seq]
GSE136693 Assessing the ability of various genomic features to prioritize causal non-coding variants associated with diseases and traits [CRISPR guide-seq]
GSE136702 Assessing the ability of various genomic features to prioritize causal non-coding variants associated with diseases and traits [MPRA]
Relations
BioProject PRJNA563093

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE136703_RAW.tar 1.0 Gb (http)(custom) TAR (of BED, BW)
SRA Run SelectorHelp
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