|
Status |
Public on Jul 01, 2024 |
Title |
ZR-75-1_Ctrl_r1 |
Sample type |
SRA |
|
|
Source name |
ZR-75-1
|
Organism |
Homo sapiens |
Characteristics |
cell line: ZR-75-1 cell type: breast cancer genotype: WT treatment: NA
|
Growth protocol |
All the cell lines were maintained in DMEM with 10% FBS and antibiotics under humidified atmosphere with 5% CO2 at 37C
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted with Trizol and 10 ug total RNA was used for downstream Dnase treatment and reverse transcription Targeted PCR was perforem with Phusion to add illumina sequencing adaptors
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|
|
Library strategy |
OTHER |
Library source |
transcriptomic |
Library selection |
other |
Instrument model |
Illumina HiSeq 4000 |
|
|
Description |
RORC RNA switch DMS reactivity
|
Data processing |
Reads from multiple lanes were merged and collapsed using fastq2collapse.pl (CTK package) UMIs were then extracted using `umi_tools extract` with --extract-method string --bc-pattern=NNNNNNNNNNN flags cutadapt (v3.5) was used to remove the constant sequences bwa (v0.7.17-r1188) was used to align the reads to the reference. Aligned reads were then sorted and deduplicated using UMICollapse (with -k 1 --algo adj --merge avgqua flags) Mutations were then counted at each position for As and Cs (common SNPs were filtered) Assembly: hg38 Supplementary files format and content: DMS signal at each position Library strategy: DMS-MaPseq
|
|
|
Submission date |
Apr 28, 2024 |
Last update date |
Jul 01, 2024 |
Contact name |
Hani Goodarzi |
Organization name |
UCSF
|
Department |
Biochemistry and Biophysics
|
Street address |
600 16th St, GH S312D
|
City |
San Francisco |
State/province |
CA |
ZIP/Postal code |
94158 |
Country |
USA |
|
|
Platform ID |
GPL20301 |
Series (2) |
GSE266051 |
DMS-MaPseq of RORC reporters and endogeneous RORC locus |
GSE266070 |
RORC RNA Switch Mechanisms |
|
Relations |
BioSample |
SAMN41105983 |
SRA |
SRX24387143 |