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Sample GSM1824696 Query DataSets for GSM1824696
Status Public on Jan 18, 2016
Title Xbp1 Knock-out (Xbp1KO) rep2, batch 2
Sample type SRA
 
Source name Bone marrow, plasma cells, Xbp1 knockout
Organism Mus musculus
Characteristics strain/background: C57BL/6
genotype/variation: Xbp1-/-
tissue: bone marrow
cell type: plasma cells
Extracted molecule total RNA
Extraction protocol RNA was isolated from ex-vivo sorted Blimp1-GFP+CD138+ plasma cells using the Qiagen RNeasy Micro kit.
Libraries were generated using the Illumina TruSeq RNA sample preparation kit following manufacturer instructions.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NextSeq 500
 
Description Xbp1KO_rep2_batch2
Data processing Sequence reads were aligned to the GRCm38/mm10 build of the Mus musculus genome using the Subread aligner. Only uniquely mapped reads were retained.
Genewise counts were obtained using featureCounts. Reads overlapping exons in annotation build 38.1 of NCBI RefSeq database were included. Ig genes were excluded from the gene-level expression analysis. Genes were filtered from downstream analysis if they failed to achieve a CPM (counts per million mapped reads) value of at least 1 in at least one library.
Counts were converted to log2 counts per million, quantile normalized and precision weighted with the 'voom' function of the limma package. A linear model was fitted to each gene, and empirical Bayes moderated t-statistics were used to assess differences in expression. Genes were called differentially expressed if they achieved a false discovery rate of 0.05 or less.
Genome_build: GRCm38 (mm10)
Supplementary_files_format_and_content: Tab-delimited text files include normalized log2-FPKM values for each library. EntrezIDs represent NCBI Entrez Gene IDs.
Supplementary_files_format_and_content: GEO_suppl_raw_counts.txt': Includes raw read counts for each gene in each library. The raw read count is the number of mapped reads (or read pairs for paired-end libraries) assigned to each gene. EntrezIDs represent NCBI Entrez Gene IDs.
 
Submission date Jul 15, 2015
Last update date May 15, 2019
Contact name Wei Shi
E-mail(s) [email protected]
Organization name Monash University
Street address Wellington Rd
City Clayton
State/province Victoria
ZIP/Postal code 3800
Country Australia
 
Platform ID GPL19057
Series (1)
GSE70981 Blimp1 controls plasma cell physiology and function
Relations
SRA SRX1098365
BioSample SAMN03863205

Supplementary file Size Download File type/resource
GSM1824696_Xbp1CreER_fl_rep2.bam.txt.gz 221.4 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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