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Series GSE75417 Query DataSets for GSE75417
Status Public on Feb 28, 2017
Title mRNA-seq analysis of B3 pre-B cell line from STATegra Project
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary The main goal of the project is to develop a new generation of bioinformatics resources for the integrative analysis of multiple types of omics data. These resources include both novel statistical methodologies as well as user-friendly software implementations. STATegra methods address many aspects of the omics data integration problem such as the design of multiomics experiments, integrative transcriptional and regulatory networks, integrative variable selection, data fusion, integration of public domain data, and integrative pathway analysis. To support method development STATegra uses a model biological system, namely the differentiation process of mouse pre-B-cells. The STATegra consortium generated data focused on a critical step in the differentiation of B lymphocytes, which are key components of the adaptive immune system. Transcription factors of the Ikaros family are central to the normal differentiation of B cell progenitors and their expression increases in response to developmental stage-specific signals to terminate the proliferation of B cell progenitors and to initiate their differentiation. In particular, a novel biological system that models the transition from the pre-BI stage to the pre-BII subsequent stage, where B cell progenitors undergo growth arrest and differentiation, was used. The approach involves a pre-B cell line, B3 , and an inducible version of the Ikaros transcription factor, Ikaros-ERt2. Ikaros factors act to down-regulate genes that drive proliferation and to simultaneously up-regulate the expression of genes that promote the differentiation of B cell progenitors. Hence, in the B3 system, before induction of Ikaros, cells proliferate and their gene expression pattern is similar to proliferating B cell progenitors in vivo. Following Ikaros induction, B3 cells undergo gene expression changes that resemble those that occur in vivo during the transition from cycling to resting pre-B cells, followed by a marked reduction in cellular proliferation and by G1 arrest. On this system the consortium has created a high-quality data collection consisting of a replicated time course using seven different omics platforms: RNA-seq, miRNA-seq, ChIP-seq, DNase-seq, Methyl-seq, proteomics and metabolomics, which is used to assess and to validate STATegra methods.
 
Overall design The STATegra experimental design consists of a 6 point, time course that captures the differentiation of B3 cells containing Ikaros-ERt2 upon Ikaros induction within a 24 hours period. The differentiation was sampled at 0h, 2h, 6h, 12h, 18h and 24h after Ikaros induction by Tamoxifen. As control, B3 cells transfected with an empty vector were treated and sampled in the same way as the inducible line. Eight different omic technologies were measured on this system: RNA-seq, miRNA-seq, DNase-seq, RRBS-seq, ChIP-seq, scRNA-seq, Proteomics and Metabolomics. Generally, three biological replicates were obtained per platform and were processed as independent batches.
Paired-end strand-specific RNA-seq analysis was performed using total RNA of 3 biological batches (1, 2 and 4) for time 0h and total RNA of 3 biological batches (1, 3 and 4) for times 2h, 6h, 12h,18h and 24h. There were two experimental conditions (C=Control, IK=Ikaros) and the 3 biological replicates per condition and time point were numbered as 1, 2 and 3. For some of these biological replicates, also technical replicates were generated in order to measure the variability between batches and afterwards correct the potential batch effect.
Web link http://www.stategra.eu/
 
Contributor(s) Merkenschlager M, Ferreiros I, Liang Z, Cooper L, Tegnér J, Gómez-Cabrero D, Fernandes S, Noori P, Silderberg G, Conesa A
Citation(s) 31672995
Submission date Nov 25, 2015
Last update date Oct 05, 2020
Contact name Ana Conesa
E-mail(s) info@stategra.eu
Organization name Centro de Investigaciones Príncipe Felipe (CIPF)
Department Computational Genomics Program
Lab Genomics and Gene Expression Lab
Street address C/ Eduardo Primo Yúfera 3
City Valencia
State/province Valencia
ZIP/Postal code 46012
Country Spain
 
Platforms (1)
GPL17021 Illumina HiSeq 2500 (Mus musculus)
Samples (36)
GSM1954785 Stategra_Control cells 0h Batch1
GSM1954786 Stategra_Control cells 0h Batch2
GSM1954787 Stategra_Control cells 0h Batch4
This SubSeries is part of SuperSeries:
GSE75395 Omics analyses of B3 pre-B cell line from STATegra Project
Relations
BioProject PRJNA304160
SRA SRP066679

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Supplementary file Size Download File type/resource
GSE75417_STATegra.RNAseq.CQN.Combat.Annotated.positive_2014_09.csv.gz 3.6 Mb (ftp)(http) CSV
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Raw data are available in SRA
Processed data are available on Series record

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