You are here: FoswikiMITOMAP WebToolLaunchpad (20 Feb 2020, UnknownUser)

New Tools!

Classic Tools and Resources

    Haplotype your sequences and get variant information - including frequencies, conservation, references, and more. Input can be sequences in FASTA format, GenBank numbers, or SNVs. The SNV query is especially useful for novel variants.

  • Allele Search
    Search for variants by position - a quick way to pull up info on general population variants and patient variants. For variants not currently listed in Mitomap, use the SNV query function in MITOMASTER, above.

  • Sequence and Variant Downloads
    Retrieve sequence IDs from our current database, from GenBank, and elsewhere. Download a real-time listing of all variants found in Mitomap's set of GenBank sequences.

  • Data Downloads
    Download raw data in various formats from the Mitomap database.

Topic revision: r1 - 20 Feb 2020, UnknownUser

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