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Series GSE201076 Query DataSets for GSE201076
Status Public on Apr 24, 2022
Title Copy number variations may contribute to congenital heart defect risk greatly by disrupting long noncoding RNAs
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary We identified lncRNAs locating in CNV locus which were coexpressed with multiple congenital heart defect associated genes. To validate our findings, we performed overexpression and knockdown experiments to characterize the trascriptomic profiles regulated by HSALNG0104472.
 
Overall design Paired RNA-seq of lncRNA HSALNG0104472 knockdown cardiomyocytes (AC16), HSALNG0104472 overexpression cardiomyocytes, control cardiomyocytes for overexpression of HSALNG0104472 and control cardiomyocytes for knockdown of HSALNG0104472. Three biological replicates were obtained for each sample.
Web link https://www.nature.com/articles/s42003-023-04565-z
 
Contributor(s) Lu Y, Fang Q, Wang B
Citation(s) 36806749
Submission date Apr 19, 2022
Last update date Mar 06, 2023
Contact name Yibo Lu
E-mail(s) wave8013@sjtu.edu.cn
Phone 18916600183
Organization name Shanghai Jiao Tong University
Department Shanghai Children's Medical Center
Street address No.1678, Dongfang Road, Shanghai
City Shanghai
ZIP/Postal code 200025
Country China
 
Platforms (1)
GPL29480 DNBSEQ-T7 (Homo sapiens)
Samples (12)
GSM6050230 290-rep1
GSM6050231 290-rep2
GSM6050232 290-rep3
Relations
BioProject PRJNA828187

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Supplementary file Size Download File type/resource
GSE201076_Featurecounts_matrix.txt.gz 541.0 Kb (ftp)(http) TXT
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