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Sample GSM7886367 Query DataSets for GSM7886367
Status Public on Jul 08, 2024
Title 21_SS111
Sample type SRA
 
Source name Retina
Organism Homo sapiens
Characteristics tissue: Retina
cell line: hTERT RPE1
cell type: epithelial cell
genotype: +chr 8; +chr 9; +chr18
Growth protocol Cells were maintained in DMEM supplemented with 10% fetal bovine serum (FBS) and 1% penicillin-streptomycin in humidified atmosphere with 5% CO2 at 37°C.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using the miRNeasy mini kit (Qiagen).
Small RNA sequencing libraries were constructed using the TruSeq Small RNA Library Prep Kit (Illumina) according to manufacturer protocol.
 
Library strategy miRNA-Seq
Library source transcriptomic
Library selection size fractionation
Instrument model Illumina NovaSeq 6000
 
Description 21_SS111
Data processing FASTQ data were trimmed using cutadapt-1.9.1; then trimmed data was aligned to custom sequence libraries listing all isoforms of small RNA molecules by using Bowtie with --best and -v 0 switches and saved in .map output format.
Isomirage software was used to count the number of occurrences in the .map file of each isoform listed in the .genome file
Assembly: custom genome, containing all human microRNAs (canonical and Isoforms)
Supplementary files format and content: raw_counts.txt: raw reads for all miRNAs in all samples
 
Submission date Nov 08, 2023
Last update date Jul 08, 2024
Contact name Francesco Nicassio
E-mail(s) francesco.nicassio@iit.it
Organization name Istituto Italiano di Tecnologia
Department Center for genomic science
Street address Via Adamello 16
City Milano
ZIP/Postal code 20139
Country Italy
 
Platform ID GPL24676
Series (1)
GSE247267 Increased RNA and protein degradation is required for counteracting transcriptional burden and proteotoxic stress in human aneuploid cells
Relations
BioSample SAMN38155304
SRA SRX22416426

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA

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