With VarSome Clinical you can process your NGS data, be it an off-the-shelf or custom gene panel, an exome or whole genome. You can start the analysis either from FASTQ or VCF.
The first step consists of uploading your sequencing data to our servers over a secure internet protocol. You can either select the files directly from your computer, or you can take advantage of the application programming interface to upload the data automatically.
Visit VarSome.com, our Global Human Genomics Community
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Documentation for VarSome Clinical
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Learn more about VarSome Clinical
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Application Notes and Whitepapers
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