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  1. Ensembl genome browser 115

    Ensembl is a public and open project providing access to genomes, annotations, tools and methods. Its goal is to enable genomic science by providing high-quality, integrated and consistent annotation on …

  2. Ensembl Plants

    Ensembl Plants is a genome-centric portal for plant species of scientific interest

  3. Ensembl Genome Browser

    Browse a Genome The Ensembl project produces genome databases for vertebrates and other eukaryotic species, and makes this information freely available online.

  4. Homo_sapiens - Ensembl genome browser 115

    Genome assembly: GRCh38.p14 (GCA_000001405.29) More information and statistics Download DNA sequence (FASTA) Convert your data to GRCh38 coordinates Display your data in Ensembl Other …

  5. About Ensembl Variation

    About Ensembl Variation The Ensembl Variation database stores areas of the genome that differ between individual genomes ("variants") and, where available, associated disease and phenotype …

  6. BLAST search — Ensembl

    BLAST stands for Basic Local Alignment Search Tool. The emphasis of this tool is to find regions of sequence similarity, which will yield functional and evolutionary clues about the structure and …

  7. Ensembl

    The new website of the Ensembl projectBeta is a fresher, faster way to see genome annotation across the taxonomic tree and get the data you need. This is the new home for both the most popular …

  8. Ensembl Training and Workshops

    Welcome to the Ensembl Training homepage, where you'll find out everything you need to know about training and workshops on working with the Ensembl Genome Browser, focussing on vertebrate …

  9. Downloads - Ensembl genome browser 115

    Write your own Perl scripts to retrieve small-to-medium datasets. All our data, as well as added functionality, is available through the Ensembl Perl API. Use the API to retrieve gene and transcript …

  10. Ensembl Variant Effect Predictor (VEP)

    Ensembl VEP predicts the effect of your variants (SNPs, insertions, deletions, CNVs or structural variants) on gene transcripts and protein sequence, as well as regulatory regions. It reports …