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Status |
Public on Mar 28, 2018 |
Title |
Analysis of gene expression profile in the control and CHD7-knockdown hiPSC-derived lt-NES cells (scRNA-Seq) |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
CHARGE syndrome is a congenital disorder caused by mutations in Chromodomain Helicase DNA-binding domain 7 (CHD7) gene. We performed single cell RNA-seq analysis in CTRL and CHD7-knockdown lt-NES cells.
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Overall design |
Single cell RNA-Seq profiling of control (shCTRL) and CHD7-knockdown (sh410 or sh411) cells.
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Citation(s) |
29440260 |
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Submission date |
Dec 19, 2017 |
Last update date |
Mar 27, 2019 |
Contact name |
Tsukasa Sanosaka |
Organization name |
Keio University School of Medicine
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Department |
Department of Physiology
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Street address |
35 Shinanomachi
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City |
Shinjuku-ku |
State/province |
Tokyo |
ZIP/Postal code |
1608582 |
Country |
Japan |
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Platforms (1) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
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Samples (92)
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This SubSeries is part of SuperSeries: |
GSE111327 |
Chromatin remodeler CHD7 regulates the stem cell identity of human neural progenitors |
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Relations |
BioProject |
PRJNA423024 |
SRA |
SRP127035 |