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Status |
Public on Jun 12, 2015 |
Title |
Disease-Associated SNPs From non-Coding Regions in Juvenile Idiopathic Arthritis Are Located Within or Adjacent to Functional Genomic Elements of Human Neutrophils and CD4+ T Cells |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing Genome binding/occupancy profiling by high throughput sequencing
|
Summary |
This SuperSeries is composed of the SubSeries listed below.
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Overall design |
Refer to individual Series
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Citation(s) |
25833190 |
|
Submission date |
Mar 13, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Lisha Zhu |
E-mail(s) |
lishazhu4508@gmail.com
|
Organization name |
UT Health Science Center at Houston
|
Street address |
7000 fannin st
|
City |
Houston |
State/province |
TX |
ZIP/Postal code |
77030 |
Country |
USA |
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Platforms (1) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
|
Samples (12)
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This SuperSeries is composed of the following SubSeries: |
GSE66895 |
Disease-Associated SNPs From non-Coding Regions in Juvenile Idiopathic Arthritis Are Located Within or Adjacent to Functional Genomic Elements of Human Neutrophils and CD4+ T Cells [RNA-Seq] |
GSE66896 |
Disease-Associated SNPs From non-Coding Regions in Juvenile Idiopathic Arthritis Are Located Within or Adjacent to Functional Genomic Elements of Human Neutrophils and CD4+ T Cells [ChIP-Seq] |
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Relations |
BioProject |
PRJNA278280 |