|
Status |
Public on Oct 21, 2012 |
Title |
HeLa mRNA-seq |
Sample type |
SRA |
|
|
Source name |
HeLa mRNA-seq
|
Organism |
Homo sapiens |
Characteristics |
cell line: HeLa
|
Treatment protocol |
HeLa cells were crosslinked on ice with UV-C (254 nm) at 400 mJ per cm2 in presence of cold PBS (4 ml per 15 cm dish).
|
Growth protocol |
HeLa cells were cultivated in 15 cm dishes in Dulbecco’s modified Eagle’s medium (DMEM) with 4,5g l-1 D-glucose supplemented with 10% FCS and antibiotics (streptomycin 100 ug ml-1 and penicillin 100 U ml-1).
|
Extracted molecule |
polyA RNA |
Extraction protocol |
Total RNA was harvested from HeLa cells using TRI Reagent (Ambion). cDNA library was generated from polyA+ selected mRNAs using Illumina TruSeq(TM) SBS v5 kit.
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
Illumina Casava1.7 software used for basecalling. CLIP-seq reads were trimmed for adaptor sequence using the Btrim software (parameters -3 -v7 -l 15). CLIP-seq and mRNA-seq reads were mapped to hg19 genome assembly (Ensembl 63) using Novoalign V2.07.11 (parameters -F ILMFQ -o SAM) and BLAT version 34 (parameter -minScore=15). All uniquely mapped reads with Novoalign and BLAT were used in subsequent processing. bedGraph files were generated using the genomeCoverageBed function v2.12.0 from BEDTools. Genome_build: hg19 Supplementary_files_format_and_content: bedGraph files
|
|
|
Submission date |
Sep 11, 2012 |
Last update date |
May 15, 2019 |
Contact name |
Herve LE HIR |
E-mail(s) |
lehir@ens.fr
|
Organization name |
IBENS
|
Department |
Functional Genomics
|
Lab |
Le Hir lab
|
Street address |
46 rue d'Ulm
|
City |
PARIS |
ZIP/Postal code |
75005 |
Country |
France |
|
|
Platform ID |
GPL11154 |
Series (1) |
GSE40778 |
CLIP-seq of eIF4AIII reveals transcriptome-wide mapping of the human exon junction complex |
|
Relations |
SRA |
SRX186079 |
BioSample |
SAMN01164168 |