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Status |
Public on Dec 07, 2020 |
Title |
RNAi of NF-YB RNA-seq Replicate 1 |
Sample type |
SRA |
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Source name |
HeLa cell line
|
Organism |
Homo sapiens |
Characteristics |
cell line: HeLa treatment: NF-YB siRNA J-010002-08-0002
|
Treatment protocol |
Cells at 25-30% confluence were transfected with 50 nM siRNA using 3.75 µL Lipofectamine 3000 Reagent (ThermoFisher) in 1.5 mL final volume of Optimem (ThermoFischer) per well.
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Growth protocol |
HeLa cells were grown in DMEM high glucose with L-glutamine (EuroClone SpA) supplemented with 10% FBS, 100 U/mL penicillin and 100 µg/mL streptomycin. The day before transfection, 0.15 × 10e6 cells/well were seeded in antibiotic-free medium in a 6-well plate.
|
Extracted molecule |
polyA RNA |
Extraction protocol |
The RNAs were extracted using TRI-reagent (Merck) and further purified with RNeasy Mini Kit (Qiagen) following the RNA clean-up protocol. Performed by Novogene. Total RNAs were poly-T purified, randomly fragmented and transformed in cDNA with NEB library preparation protocol.
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 4000 |
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|
Data processing |
Alignment performed with bowtie2 within rsem-calculate-expression against hg19 transcriptome. Gene quantification performed with rsem-calculate-expression. Genome_build: hg19 (GRCh37) Supplementary_files_format_and_content: *.genes.results.txt: Tab-delimited text files containing gene expression as counts, TPM and FPKM for each sample.
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Submission date |
May 26, 2020 |
Last update date |
Dec 08, 2020 |
Contact name |
Diletta Dolfini |
E-mail(s) |
diletta.dolfini@unimi.it
|
Organization name |
University of Milan
|
Department |
Bioscience
|
Street address |
Via Celoria, 26
|
City |
Milano |
State/province |
MI |
ZIP/Postal code |
20133 |
Country |
Italy |
|
|
Platform ID |
GPL20301 |
Series (1) |
GSE151237 |
On the NF-Y regulome as in ENCODE (2019) |
|
Relations |
BioSample |
SAMN15028111 |
SRA |
SRX8402223 |