All genome sequencing technologies have some degree of error in their results. This tool is designed to take the data you have uploaded from a variety of sources (SNP, WGS, etc) and look for disagreements in results. The generated report will display a detailed report of which calls have disagreed with each other between the genomes you provide. Notes: At the moment, this tool only works on data encoded using the VCF format. It is a work in progress, so be sure to look at the raw data lines if you think a disagreement might be in error.
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