Search 1000Genomes
The 1000 Genomes Browser
Ensembl-based browser provides early access to 1000genomes data
In order to facilitate immediate analysis of the 1000genomes data by the whole scientific community, this browser (based on Ensembl) integrates the SNP calls and read coverage from this December 2008 release. All of this data has been submitted to dbSNP, and once rsid's have been allocated, will be absorbed into the UCSC and Ensembl browsers according to their respective release cycles. Until that point any SNP id's on this site are temporary and will NOT be maintained.
Start Browsing 1000 Genomes data
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Browse Human → NCBI 36 |
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Transcript SNP view → View the consequences of sequence variation at the level of each transcript in the genome. |
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SeqAlignView → Shows read-depth data alongside SNPs |
Links
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1000 Genomes → More information about the 1000 Genomes Project on the 1000 genomes main site. |
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1000 Genomes Wiki → Browse the 1000 Genomes Wiki. |
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NHGRI → National Human Genome Research Institute |
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NCBI → National Center for Biotechnology Information |
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EMBL - EBI → European Bioinformatics Institute |
Data Access
The 1000 Genomes Browser displays SNP calls on CEU and YRI high coverage individuals from the December 2008 release of data from Pilot 2
The 1000 Genomes Project is an international collaborative project
described
at www.1000genomes.org. The
1000 Genomes Browser is based on Ensembl web code
Ensembl is a joint project of
and the
Wellcome Trust
Sanger Institute
and the
Wellcome Trust
Sanger Institute
