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Status |
Public on Oct 10, 2019 |
Title |
Control_350nM Dox-2 |
Sample type |
SRA |
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Source name |
Control_350nM Dox, HFFs
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Organism |
Homo sapiens |
Characteristics |
cell type: Human Foreskin Fibroblasts (HFF) crispr-cas9 targets: sgControl+sgControl treatment: 350 nM Doxorubicin bio repeat: 2
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Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was isolated from HFFs using Qiagen RNeasy plus kit, treated with DNAse (Turbo DNA-free, Life Technologies), and quality control checked using Qubit, TapeStation, and qPCR. Libraries were prepared using Kappa stranded mRNA Hyper Prep
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NextSeq 500 |
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Data processing |
Reads were mapped to the Hg19 genome by STAR. HTseq was used to generate count file with gene names(53). R package DESeq2 was used to normalize counts (mean-ratio method), calculate total reads, and determine differential gene expression(54). MA plots were generated to display differentially expressed genes. Principal component analysis showed sufficient clustering of biological replicates. Genome_build: hg19 Supplementary_files_format_and_content: DESeq2 normalized reads
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Submission date |
Mar 22, 2019 |
Last update date |
Oct 10, 2019 |
Contact name |
Amy E Schade |
E-mail(s) |
[email protected]
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Organization name |
Brigham and Women's Hospital
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Department |
Medicine
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Lab |
Karen Cichowski
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Street address |
77 Avenue Louis Pasteur
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City |
Boston |
State/province |
MA |
ZIP/Postal code |
02215 |
Country |
USA |
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Platform ID |
GPL18573 |
Series (1) |
GSE128711 |
RNA-seq of human foreskin fibroblast cells lacking RB and/or p130 after doxorubicin treatment |
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Relations |
BioSample |
SAMN11233313 |
SRA |
SRX5559760 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
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