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Sample GSM7089883 Query DataSets for GSM7089883
Status Public on Jul 14, 2023
Title NCI-H1975 + sequins mixA mixed with HCC827 + sequins mixB in ratio 50:50
Sample type SRA
 
Source name Lung adenocarcinoma
Organism Homo sapiens
Characteristics tissue: Lung adenocarcinoma
cell line: NCI-H1975, HCC827
Treatment protocol Cells were dissociated into single cell suspensions in FACS buffer, centrifuged and frozen at -80 °C.
Growth protocol The cell lines were retrieved from the ATCC (https://www.atcc.org/) and cultured in Roswell Park Memorial Institute (RPMI) 1640 medium with 10% fetal calf serum and 1% penicillin-streptomycin. The cells were grown independently at 37°C with 5% carbon dioxide until near 100% confluency.
Extracted molecule total RNA
Extraction protocol The mRNA was extracted using a Qiagen RNA miniprep kit and purified using the NEBNext® Poly(A) mRNA Magnetic Isolation Module (E7490).
The NCI-H1975+sequins mixA replicate 1 RNA was mixed with the HCC827+sequins mixB replicate 1 RNA in the 5 following mass ratios: 100:0, 75:25, 50:50, 25:75 and 0:100. 1 ng of each mix was then used for library preparation. The cRNA-PCR Barcoding (SQK-PCS109 with SQK-PBK004) kit was used with the supplied ONT protocol. Amplication for purified mRNA spiked with sequins was done with 16 PCR cycles with a 2 minutes and 30 seconds extension step and a 0.8X final bead clean up. Size selection was performed for the standard ~2kb target. 65 ng of the final library were loaded onto 1 FLO-PRO002 PromethION flow cell (R9.4.1).
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model PromethION
 
Data processing Reads were basecalled with Guppy 6.2.1 in `sup’ accuracy (dna_r9.4.1_450bps_sup_prom.cfg), disabling trimming and enabling read splitting.
Passed reads were aligned to the Gencode V33 reference transcriptome and RNA sequin annotation 2.4 with minimap2 version 2.24.
Transcript-level counts were obtained using salmon version 1.9.0.
Assembly: GrCh38 and RNA sequin annotation 2.4
Supplementary files format and content: Tab-separated files with transcript IDs, lengths and read counts
 
Submission date Mar 09, 2023
Last update date Jul 15, 2023
Contact name Matthew Ritchie
E-mail(s) [email protected]
Organization name The Walter and Eliza Hall Institute of Medical Research
Street address 1G Royal Parade
City Parkville
State/province Victoria
ZIP/Postal code 3052
Country Australia
 
Platform ID GPL26167
Series (1)
GSE227000 Long-read transcriptome profiling of human lung cancer cell lines
Relations
BioSample SAMN33698271
SRA SRX19610928

Supplementary file Size Download File type/resource
GSM7089883_barcode03.tsv.gz 1.4 Mb (ftp)(http) TSV
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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