NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM4079794 Query DataSets for GSM4079794
Status Public on Sep 17, 2019
Title DNp63-overexpressed LK2 cells_1 [OE_1]
Sample type SRA
 
Source name DNp63-overexpressed LK2 cells
Organism Homo sapiens
Characteristics cell line: LK2
cell type: lung squamous cell carcinoma (LUSC) cell lines
genotype/variation: pLEX_306-DNp63
Treatment protocol For inducible DNp63-expressing LK2 cells, cells were treated with or without 2 μg/ml doxycycline for 6 days.
Growth protocol LK2 cells were maintained in RPMI-1640 with 10% fetal bovine serum and 1% penicillin–streptomycin.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using the Qiagen RNeasy kit. Poly-adenylated RNA was enriched from 1ug of RNA with the NEBNext PolyA mRNA Magnetic Isolation Module, incubated at 94°C for 15 min and double-strand cDNA was synthesized using SuperScript III reverse transcriptase (ThermoFisher) and NEBNext® Ultra™ II Directional RNA Second Strand Synthesis Module.
Up to 10 ng of cDNA was used for the library construction using NEBNext Ultra II DNA Library Prep Kit. The finished double strand DNA libraries were quantified by Agilent Bioanalyzer according to manufacturer’s protocol. Uniquely indexed libraries were pooled in equimolar ratios and sequenced on an Illumina NextSeq500 with paired-end 38bp reads.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NextSeq 500
 
Description LK2_DNp63_1
Data processing Sequencing reads were aligned to the human reference genome hg19/GRCh37 using Tophat (v2.1).
Read counts per RefGene symbol on the USCS database was estimated using the htseq-count function in SAMtools.
The read counts were normalized using DEseq2 normalization algorithm.
Genome_build: hg19/GRCh37 RefGene
Supplementary_files_format_and_content: Text files
 
Submission date Sep 16, 2019
Last update date Sep 17, 2019
Contact name Hideo Watanabe
E-mail(s) [email protected]
Organization name Icahn School of Medicine at Mount Sinai
Department Department of Medicine, Division of Pulmonary, Critical Care and Sleep Medicine
Lab Hideo Watanabe
Street address One Gustave L. Levy Place
City New York
State/province NY
ZIP/Postal code 10029
Country USA
 
Platform ID GPL18573
Series (2)
GSE137460 Identification of a unique subtype of lung squamous cell carcinoma defined by SOX2 and a neural differentiation factor BRN2 [RNA-seq]
GSE137461 Identification of a unique subtype of lung squamous cell carcinoma defined by SOX2 and a neural differentiation factor BRN2
Relations
BioSample SAMN12757129
SRA SRX6852826

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

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap