Mouse Genomes Project

Data release policy

The Mouse Genomes Project releases sequence data, SNPs and other variant calls as a service to the research community.

These data are released in accordance with the Fort Lauderdale agreement and Toronto agreements. As producers of these data we reserve the right to be the first to publish a genome-wide analysis of the data we have generated.

The pre-publication data that we release via this website is embargoed for publication except for analyses of single chromosomes in single strains or single gene loci across multiple strains. We strongly encourage researchers to contact us if there are any queries about referencing or publishing analysis based on pre-publication data obtained via this website.

More information on the Wellcome Trust Sanger Institute's data sharing policy.

Enquiries

For further information, please contact mousegenomes@sanger.ac.uk

Latest News

  • 2011-11-17 FVB Strain Sequenced
    We have completed sequencing of the FVB/NJ strain to 53x sequence coverage. SNP, indel, and structural variation calls will be posted soon. The raw data is available for download from our ftp site and can browsed in LookSeq.
  • 2011-09-15 Nature Publications
    We are delighted to announce that two papers have been published in Nature describing the variation found and its impact on mouse phenotypes and traits. Further details.
  • 2011-08-05 Structural Variation Calls
    The entire set of structural variation calls across the 17 strains have been posted on our ftp site in the current_svs directory. These have also been submitted to DGVa under accession estd118.
  • 2011-06-30 Whole-brain RNA-seq BAMs
    We have just posted the BAM files and top-hat expression values for the whole-brain RNA-Seq data on our ftp site in the current_rna_bams directory. Note this data is also available from the ENA under accession ERP000614
  • 2011-06-27 Multi-tissue RNA-Seq
    We have recently completed RNA-Seq from a cross of C57BL/6J and DBA/2J across 6 different tissues and this data is available from the ENA under accession ERP000591
  • 2011-06-24 Whole-brain RNA-Seq
    We have recently completed sequencing whole-brain RNA from 15 of the strains using the Illumina RNA-Seq protocol. The data has been accessioned at the ENA under ERP000614.
  • 2011-06-24 Long Fragment end Sequencing
    We have recently completed sequencing the ends of 3kb fragments on the illumina platform across the mouse strains. The data is available from the ENA under study accession ERP000255
  • 2011-06-23 Variant Release & dbSNP
    We have made the final release of the SNP and short indel variants. The only change from the previous release (REL-1101) is that we have filtered out chrY calls. These SNPs and indels have been submitted to dbSNP as the final published set. The SNPs and short indels are available from our ftp site. The BAM alignment files have not been changed.
  • 2011-06-22 Accession Numbers
    The raw data has all been submitted to the ENA and the accession numbers and links are listed with the strain names.
  • 2010-07-27 Variant Releases
    The variant calls have been steadily updated over the past few months. The Data Release section below has links to all of the latest sets of SNP and short indel calls and the online browser has also been updated to reflect the new callsets. The BAM alignment files have not been changed.
  • 2010-01-13 New release
    The new release data have been loaded and are visible in the SNP query and LookSeq pages. 14 of the 17 strains are over 20x coverage (three over 30x) with the others (129S5, NZO, and WSB) all over 15x.
  • 2009-12-11 New Sequencing Data
    We have made a new freeze of the sequencing data with almost all of the strains sequenced to over 20x depth. This new data has now been loaded into the Lookseq viewer. We are preparing new SNP/indel calls and hope to have these searchable very soon.
  • 2009-11-03 IMGC
    Here is the poster we presented at IMGC
  • 2009-11-03 Sequencing Progress
    We now have 10 strains over 20x sequencing depth and have begun to prepare a new data release (SNP, indel, SV calls) for these strains. We'll post and update when the new data has been loaded.
* quick link - http://q.sanger.ac.uk/viht3vda