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Sample GSM4061726 Query DataSets for GSM4061726
Status Public on Nov 01, 2019
Title HCC827_AKT1
Sample type SRA
 
Source name HCC827 cell line, NSCLC
Organism Homo sapiens
Characteristics cell line: HCC827
treatment: AKT1
Extracted molecule total RNA
Extraction protocol RNA was harvested using Trizol reagent. RNA was prepared by using Ribo-Zero Magnetic Kit (rRNA-depleted RNA). Illumina TruSeq Stranded mRNA Kit was used for the construction of sequencing libraries.
RNA libraries were prepared for sequencing using standard Illumina protocols
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NovaSeq 6000
 
Data processing Bustard software used for basecalling.
Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence, then mapped to HG38 whole genome using bowtie2.
Reads Per Kilobase of exon per Megabase of library size (RPKM) were calculated by using HTseq.
Genome_build: HG38
Supplementary_files_format_and_content: Tab-delimited text files include RPKM values for each samples were attached.
 
Submission date Sep 05, 2019
Last update date Nov 02, 2019
Contact name Han Tian
E-mail(s) tianhan@mail2.sysu.edu.cn
Phone 86-20-87333587
Organization name Sun Yat-sen University
Department Zhongshan School of Medicine
Street address No.74, Zhongshan Er Road
City Guangzhou
State/province Guangdong
ZIP/Postal code 510080
Country China
 
Platform ID GPL24676
Series (1)
GSE136904 Strand specific Sequencing of myr-Akt1 induced transcriptomes in NSCLC cell lines
Relations
BioSample SAMN12698164
SRA SRX6804715

Supplementary file Size Download File type/resource
GSM4061726_HCC827_AKT1.txt.gz 259.9 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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