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Series GSE262189 Query DataSets for GSE262189
Status Public on Sep 17, 2024
Title Joint single-nucleus RNA sequencing and single-nucleus ATAC sequencing of neuroblastoma cell lines
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Genome binding/occupancy profiling by high throughput sequencing
Summary This study was undertaken to assess transcriptional and epigenetic heterogeneity a the level of individual cells within neuroblastoma cell lines, and to compare cell lines with MYCN amplificaion to cell lines without MYCN amplification. Methods: We used 10X Genomics multiome sequencing technology to perform joint gene expression and ATAC profiling on thousands of nuclei isolated from the following human neuoblastoma cell lines: SHSY5Y, SK-N-AS, SK-N-SH, SK-N-DZ, Be-2c, and CHP134. Results: We found considerable gene expression and epigeneic heterogeneity both within and between neuroblastoma cell lines. Conclusion: Joint single-nucleus RNA sequencing and single-nucleus ATAC sequencing has demonsrated that neuroblastoma cell lines are heterogeneous, which may have implications for therapeutic strategies.
 
Overall design Use of 10X Genomics muliome sequencing technology (GEX + ATAC) to analyze single-cell transcriptomics and single-cell epigenetics of neuroblastoma cell lines.
 
Contributor(s) Goldstein AM, Guyer RA
Citation(s) 39511250
Submission date Mar 21, 2024
Last update date Dec 17, 2024
Contact name Allan M Goldstein
E-mail(s) amgoldstein@partners.org
Phone 617-726-0270
Organization name Massachusetts General Hospital
Department Pediatric Surgery
Lab Goldstein Lab
Street address 185 Cambridge St
City Boston
State/province MA
ZIP/Postal code 02114
Country USA
 
Platforms (1)
GPL24676 Illumina NovaSeq 6000 (Homo sapiens)
Samples (12)
GSM8159270 Be2c ATAC
GSM8159271 Be2c GEX
GSM8159272 CHP134 ATAC
Relations
BioProject PRJNA1090535

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Supplementary file Size Download File type/resource
GSE262189_RAW.tar 26.8 Gb (http)(custom) TAR (of CSV, H5, TBI, TSV)
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Raw data are available in SRA

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