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Status |
Public on Nov 01, 2019 |
Title |
HCC827_AKT1 |
Sample type |
SRA |
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Source name |
HCC827 cell line, NSCLC
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Organism |
Homo sapiens |
Characteristics |
cell line: HCC827 treatment: AKT1
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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
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
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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.
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Submission date |
Sep 05, 2019 |
Last update date |
Nov 02, 2019 |
Contact name |
Han Tian |
E-mail(s) |
tianhan@mail2.sysu.edu.cn
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Phone |
86-20-87333587
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Organization name |
Sun Yat-sen University
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Department |
Zhongshan School of Medicine
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Street address |
No.74, Zhongshan Er Road
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City |
Guangzhou |
State/province |
Guangdong |
ZIP/Postal code |
510080 |
Country |
China |
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Platform ID |
GPL24676 |
Series (1) |
GSE136904 |
Strand specific Sequencing of myr-Akt1 induced transcriptomes in NSCLC cell lines |
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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 Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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