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Series GSE212027 Query DataSets for GSE212027
Status Public on Jun 30, 2024
Title Transcriptome analysis in B16F10 and 4T1 cell lines with decitabine treatment [RNA-seq]
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary The goal of RNA-seq is to identify the differential expressed genes in the B16F10 and 4T1 cells after Decitabine treatment. Three biological replicates were assigned for each group and in total 12 groups were prepared for RNA-seq libraries with 300 ng mRNA as starting materials using NEXTflex Illumina qRNA-Seq Library Prep Kit (Bioo Scientific). We mapped over 60 million reads per sample to mouse genome (mm10) with RSEM workflow. P-values of differential expression were adjusted for multiple-hypothesis testing using False Discovery Rate (FDR) method.
 
Overall design Messenger RNA from B16F10 and 4T1 cell lines were extacted and cDNA libraries were generated for deep sequencing, in triplicate, using HiSeq 4000 or NovaSeq S4
 
Contributor(s) Zhang Y, Wang SY
Citation(s) 39169233
Submission date Aug 25, 2022
Last update date Sep 30, 2024
Contact name Eric Greer
E-mail(s) [email protected]
Organization name Boston Children's Hospital/Harvard Medical School
Department Newborn Medicine/Department of Pediatrics
Lab Greer Lab
Street address 320 Longwood Avenue
City Boston
State/province MA
ZIP/Postal code 02115
Country USA
 
Platforms (2)
GPL21103 Illumina HiSeq 4000 (Mus musculus)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
Samples (12)
GSM6507523 B16F10 control replicate 1 [RNA-seq]
GSM6507524 B16F10 control replicate 2 [RNA-seq]
GSM6507525 B16F10 control replicate 3 [RNA-seq]
This SubSeries is part of SuperSeries:
GSE212029 B16 and 4T1 cell lines with decitabine treatment
Relations
BioProject PRJNA873589

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Supplementary file Size Download File type/resource
GSE212027_B16_and_4T1_raw_counts.xlsx 4.3 Mb (ftp)(http) XLSX
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Raw data are available in SRA
Processed data are available on Series record

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