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Sample GSM7731450 Query DataSets for GSM7731450
Status Public on Mar 29, 2024
Title snATAC-Seq Hypothalamic Cells, rs7132908 AA, Differentiation 2, Replicate 1
Sample type SRA
 
Source name Hypothalamic cells
Organism Homo sapiens
Characteristics cell type: Hypothalamic cells
genetic modification: rs7132908 G>A
Sex: Female
Extracted molecule genomic DNA
Extraction protocol Nuclei were isolated from each sample following 10X Genomics Chromium Single Cell Multiome ATAC + Gene Expression protocols
Libraries were prepared following the 10X Genomics Chromium Single Cell Multiome ATAC + Gene Expression workflow, according to manufacturer's instructions.
 
Library strategy ATAC-seq
Library source genomic
Library selection other
Instrument model Illumina NovaSeq 6000
 
Description AA2
Data processing .fastq files were generated with Cell Ranger ARC version 2.0.2 -mkfastq
.fastq files were aligned to GRCh38 and cells were called using Cell Ranger ARC version 2.0.2 with parameters -count --min-atac-count=2000 --min-gex-count=1000
Cells underwent quality control with SoupX version 1.6.2, Scrublet version 0.2.3 and Seurat version 4.3.0
Samples were integrated with SCTransform version 0.3.5 and then Harmony version 0.1.1 was used for batch correction
Assembly: GRCh38
Supplementary files format and content: barcode.tsv contains 10X barcodes used to identify cells, features.tsv contains peak location, matrix.tx contains read counts for all cells
 
Submission date Aug 23, 2023
Last update date Mar 29, 2024
Contact name Sheridan Hope Littleton
E-mail(s) sl2225@cam.ac.uk
Organization name University of Cambridge
Department Clinical Biochemistry
Lab Giles Yeo
Street address Robinson Way
City Cambridge
ZIP/Postal code CB2 0SL
Country United Kingdom
 
Platform ID GPL24676
Series (2)
GSE241593 Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3’ UTR of FAIM2 (snATAC-Seq)
GSE241691 Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3’ UTR of FAIM2
Relations
BioSample SAMN37130026
SRA SRX21475337

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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