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Sample GSM6372291 Query DataSets for GSM6372291
Status Public on Jun 20, 2024
Title siFBL_rep2_12h
Sample type SRA
 
Source name HEK293T cell line
Organism Homo sapiens
Characteristics cell line: HEK293T
sirna: siFBL
time point: 12h
Extracted molecule polyA RNA
Extraction protocol RNA was extracted from the HEK293T and C4-2 cells.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model BGISEQ-500
 
Data processing mRNA half-life of the HEK293T cells and C4-2 cells was computed as described before. In short, the mRNA levels were first normalized to RPKM (Reads Per Kilobase Million). To reduce the noise due to genes that showed a higher expression levels after inhibition of transcription, we then scaled the FPKM values based on the expression levels of top 10 genes which were most stable between time points, so that these genes will have no change of expression between time points. The RNA degradation rate kdecay was defined as the mean values of ratio from RPKM at time 0 over the RPKM value at each other time point (0hour, 6hour, 12hour, 24hour). After that the pseudo-mRNA half-life t1/2 was calculated as ln2/kdecay.
After base-calling using guppy_basecaller (version 3.6.1), the direct RNA-seq of Nanopore reads with quality value more than 7 were aligned to the human genome (Hg38, GRCh38.p13 from GENCODE database) using Minimap with --secondary=no -ax splice -uf -k14 option. Tombo resquiggle was used to assigned to transcript sequence as reference from the website: https://www.gencodegenes.org/human . We extracted the median, standard deviation, mean, and dwell time from Nanopore raw signal data in each direct RNA sequencing read to calculate the probability of Nm modification using the training models from rRNA. The modified base supported by at least 5 modified transcripts were identified as modified Nm sites.
Assembly: hg19 for NGS RNA-seq. hg38 for Nanopore RNA-seq.
Supplementary files format and content: *.count.txt: Tab-delimited text files include abundance measurements.
Supplementary files format and content: *.bw: bigWig files.
 
Submission date Jul 21, 2022
Last update date Jun 20, 2024
Contact name Yanqiang Li
Organization name Boston Children's Hospital
Department Cardiology Department
Lab Kaifu Chen Lab
Street address 300 Longwood Ave.
City Boston
State/province MA
ZIP/Postal code 02115
Country USA
 
Platform ID GPL23227
Series (1)
GSE208837 FBL catalyzes internal 2′-O-Methylation in mRNA to promote RNA stability
Relations
BioSample SAMN29881672
SRA SRX16407269

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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