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Sample GSM1021224 Query DataSets for GSM1021224
Status Public on Nov 01, 2013
Title Young_1_RNAseq
Sample type SRA
 
Source name Bone Marrow
Organism Mus musculus
Characteristics cell type: Haematopoietic Stem Cells
strain: C57BL/6
age: Young - 8 - 12 weeks
Extracted molecule polyA RNA
Extraction protocol We sorted lower side population cells (LSPs) from adult female wild-type C57b/6 mice at different time points and extracted DNA and RNA simultaneously from the same cells. DNA library prep was performed using NEB library prep kits for illumina and mRNA library prep was completed using the Illumina Tru-seq library prep kit
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina Genome Analyzer II
 
Description RNA-(Tru)seq
Data processing The MeDIP-seq data were analysed within the MeDUSA pipeline (Wilson et al. 2012)
Alignment was performed using BWA v0.5.8 with default parameters
Filtering was performed using SAMtools to remove reads with low alignment score. Only those forming a correctly aligned pair were kept. A final filtering step removed potential PCR artefacts by discarding all but one read-pair within groups of non-unique fragments.
Wig files were created using the MEDIPS v1.0 bioconductor package. Bigwig files generated by converting wig files generated in MEDIPS using wigToBigWig from UCSC.
The RNA-Seq data were analysed using RSEM v1.1.21
RNA-seq data was aligned against a transcriptome library using BOWTIE v0.12.7 with default parameters. Transcript library built using RSEM v1.1.21 utilising UCSC mm9 annotation (from UCSC table 'knownGene')
Isoform counts were generated from the aligned RNA-seq data using RSEM (http://deweylab.biostat.wisc.edu/rsem/) utilising the UCSC known gene table for mm9.
Gene counts and isoform counts .results files output from RSEM
Genome_build: mm9
Supplementary_files_format_and_content: .bw file scores represent normalised (reads per million) read depth across the genome.
Supplementary_files_format_and_content: .results files represent gene counts and isoform counts. Headers for the output genes.results are 'internal_gene_id', 'expected_counts', 'tau_value', 'ucsc_transcript_id_list'. Headers for the output isoforms.results are 'ucsc transcript_id', 'expected_counts', 'tau_value', 'internal_gene_id'.
 
Submission date Oct 17, 2012
Last update date May 15, 2019
Contact name Gareth Wilson
E-mail(s) gareth.wilson@ucl.ac.uk
Organization name UCL Cancer Institute
Street address 23 Huntley Street
City London
ZIP/Postal code WC1E 6BT
Country United Kingdom
 
Platform ID GPL9250
Series (1)
GSE41658 Methylomic analysis identifies the involvement of migration and adhesion genes in the ageing of primary haematopoietic stem cells
Relations
Reanalyzed by GSE80797
SRA SRX196447
BioSample SAMN01766998

Supplementary file Size Download File type/resource
GSM1021224_Y_B6_out_genes.Results.txt.gz 464.1 Kb (ftp)(http) TXT
GSM1021224_Y_B6_out_isoforms.Results.txt.gz 720.0 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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