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Sample GSM3449974 Query DataSets for GSM3449974
Status Public on Nov 10, 2018
Title HeLa_RNAseq_totalRNA
Sample type SRA
 
Source name cervical cancer cells
Organism Homo sapiens
Characteristics cell line: HeLa
Growth protocol HeLa cells (from ATCC) were cultured in DMEM (HyClone, SH30243.01) supplemented with 10% FBS (HyClone, SH30084.03) and 100 U ml-1 penicillin-streptomycin (HyClone, SV30010) and maintained in a incubator at 37˚C and 5% CO2.
Extracted molecule total RNA
Extraction protocol Cells were UV-crosslinked and lysed, and RNA-protein complexes were isolated with magnetic beads.
cDNA libraries were prepared for sequencing using standard Illumina protocols.
 
Library strategy OTHER
Library source transcriptomic
Library selection other
Instrument model BGISEQ-500
 
Description total RNA
Data processing Library strategy: PBS-R
Illumina Casava1.7 software used for basecalling.
The reads were mapped to the hg19 human reference genome using the HISAT aligner.
Bowtie2 and RSEM were used to analyze gene expression, and MACS was used for peak calling.
Genome_build: hg19
Supplementary_files_format_and_content: AllSamples_FPKM txt file include FPKM values for each Sample, and RPBS_peaks txt file include peaks information of protein binding sites on RNAs.
 
Submission date Oct 29, 2018
Last update date Nov 10, 2018
Contact name Liu Fenglin
E-mail(s) liufl@ioz.ac.cn
Phone 15001248122
Organization name Chinese Academy of Sciences
Street address Courtyard 1, Beichen West Road
City Beijing
ZIP/Postal code 100101
Country China
 
Platform ID GPL23227
Series (1)
GSE121919 Genome-wide identification of protein binding sites on RNAs in mammalian cells [PBS-R]
Relations
BioSample SAMN10341907
SRA SRX4949959

Supplementary file Size Download File type/resource
GSM3449974_AllSamples_FPKM.txt.txt.gz 1.9 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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