|
| Status |
Public on Mar 02, 2018 |
| Title |
aCGH data from SCEC and corresponding normal samples |
| Organism |
Homo sapiens |
| Experiment type |
Genome variation profiling by genome tiling array
|
| Summary |
Primary SCEC is a rare malignancy without established treatment strategy. Although previous studies suggested that there were similarities between SCEC and SCLC in clinical manifestation and pathological morphology, genetic studies on this highly malignant tumour remains sparse.
This study was designed to investigate the copy number variations (CNVs) of SCEC.
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| |
|
| Overall design |
SCEC vs.corresponding normal samples. Biological replicates: 3 SCEC replicates, 3 control replicates.
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| |
|
| Contributor(s) |
Liu D, Chen J, Fan M |
| Citation(s) |
30228821 |
| Submission date |
Mar 01, 2018 |
| Last update date |
Jul 19, 2019 |
| Contact name |
Juan Wang |
| E-mail(s) |
wangj@rainbow-genome.com
|
| Organization name |
Shanghai Jiayin Biotechnology Co., Ltd.
|
| Street address |
No. 135 Guowei Road
|
| City |
Shanghai |
| ZIP/Postal code |
200438 |
| Country |
China |
| |
|
| Platforms (1) |
| GPL10123 |
Agilent-022060 SurePrint G3 Human CGH Microarray 4x180K (Feature Number version) |
|
| Samples (3) |
| GSM3028082 |
SCEC and corresponding normal tissue, replicate 1 |
| GSM3028083 |
SCEC and corresponding normal tissue, replicate 2 |
| GSM3028084 |
SCEC and corresponding normal tissue, replicate 3 |
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| This SubSeries is part of SuperSeries: |
| GSE111299 |
Genome-wide analysis of gene expression and DNA copy number variations in small cell esophageal carcinoma |
|
| Relations |
| BioProject |
PRJNA436496 |
