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160; Feedback to us. The map-based sequence of the rice genome.
Welcome to our wiki! If you would like to contribute, log-in. We recommend using your e-mail address or Michigan uniqname as your user id. For basic instructions, see the Wikipedia Tutorial. We are developing software tools. For the analysis of next generation sequence data. Variant Calling and De Novo Mutation Detection in Families with Polymutt. Rare Variant Analysis using RvTests.
Rapidly align sequences to the genome. Download data from the Genome Browser database. Get functional effect predictions for variant calls. Combine data sources from the Genome Browser database. Find genes that are similar by expression and other metrics. Run the Genome Browser on your laptop or server. Rapidly align PCR primer pairs to the genome. Convert genome coordinates between assemblies.