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Status |
Public on Dec 22, 2024 |
Title |
Kuramochi, DMSO, rep 2 |
Sample type |
SRA |
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Source name |
Kuramochi
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Organism |
Homo sapiens |
Characteristics |
cell line: Kuramochi cell type: ovarian cancer treatment: DMSO
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Extracted molecule |
total RNA |
Extraction protocol |
Messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads After fragmentation, the first strand cDNA was synthesized using random hexamer primers followed by the second strand cDNA synthesis. The library was ready after end repair, A-tailing, adapter ligation, size selection, amplification, and purification.
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2000 |
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Data processing |
nf-core/rnaseq version 3.3. Assembly: GRCh38 Supplementary files format and content: Tab delimited text files, contain raw read counts at isoform level.
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Submission date |
Nov 13, 2024 |
Last update date |
Dec 22, 2024 |
Contact name |
Jianxin Wang |
Organization name |
Roswell Park Comprehensive Cancer Center
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Department |
Molecular and Cellular Biology
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Street address |
665 Elm Street
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City |
Buffalo |
State/province |
NY |
ZIP/Postal code |
14203 |
Country |
USA |
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Platform ID |
GPL11154 |
Series (1) |
GSE281746 |
Differential responses to selective CDK2 inhibitor BLU-222 is conditioned by tumor suppressors |
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Relations |
BioSample |
SAMN44716899 |
SRA |
SRX26704701 |
Supplementary file |
Size |
Download |
File type/resource |
GSM8627467_Kuramochi_DMSO_2.isoforms.results.gz |
3.4 Mb |
(ftp)(http) |
RESULTS |
SRA Run Selector |
Raw data are available in SRA |
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